SlideShare a Scribd company logo
SENSORY RECEPTORS
• Student should be able to
• understand the types of sensory receptors
• enumerate and understand the properties of
receptors
SENSORY RECEPTORS
• Information about the internal and external environment activates
the CNS via a variety of sensory receptors.
• These receptors are transducers that convert various forms of
energy in the environment into action potentials in neurons.
• Stimulus is an event or particular form of energy that evokes a
specific functional reaction in an organ or receptor. (mechanical,
chemical, EMG, temp)
SENSE ORGANS
• Receptors are dendritic endings of afferent
neurons that are associated with non-neuronal
cells forming sense organs.
• The term Sensory unit
means sensory axon and
all its peripheral
branches.
• The receptive field of
a sensory neuron is the
particular part of the
body surface in which
a stimulus will trigger the
firing of that neuron.
CLASSIFICATION OF SENSORY
RECEPTORSTYPE OF SENSATION
• Mechanoreceptors
• Thermoreceptors
• Nociceptors
• Electromagnetic
• Chemoreceptors
DISTANCE OF
PERCEPTION
• Teleceptors
• Exteroceptors
• Interoceptors
• Proprioceptors
CLASSIFICATION OF RECEPTORS
• Mechanoreceptors
Epidermis & dermis
Joints, tendons, ligaments & muscles
Cochlea
Vestibular apparatus
Baroreceptors in vessels
• Thermoreceptors
Warmth & cold
• Nociceptors
Pain
• Electromagnetic
Rods & cones
• Chemoreceptors
Taste & smell
Carotid &aortic bodies
Hypothalamus
Osmo receptors
TACTILE MECHANORECEPTORSENCAPSULATED
• Meissner’s corpuscles in
dermal papilla
• Pacinian corpuscles in dermis,
ligaments, joint capaules
• Ruffni’s end organs in dermis
and in deeper tissues
NON-ENCAPSULATED
• Free nerve endings in
dermis, ligaments,
cornea, bones
• Hair end organs in hairy
skin
• Merkel’s discs in non
hairy and hairy skin
Mechanoreceptors
Skin (epidermis,
dermis)
Deeper tissues
SENSORY CODING
Receptors encode four elements of stimuli
• Modality
• Location
• Intensity
• Duration
MODALITY OF SENSATION
• Differential Sensitivity of Receptors for particular
stimulus or specific energy for which it is designed
• When nerve fiber from the receptors is stimulated the
perception is that for which the receptor is specialized,
no matter where and how that nerve is stimulated. This
is Muller’s law of specific energy.
• The specificity of nerve fibers for transmitting only one
modality of sensation is called the labeled line principle.
EXPLANNATION
• Each nerve tract terminates at a specific point in the
central nervous system, and the type of sensation felt
when a nerve fiber is stimulated is determined by the
point in the nervous system to which the fiber leads.
• For instance if a pain fiber is stimulated, the person
perceives pain regardless of what type of stimulus
excites the fiber.
• Likewise, if a touch fiber is stimulated by electrical
excitation of a touch receptor or in any other way, the
person perceives touch.
LAW OF PROJECTION
• No matter which part of a pathway you
stimulate between the receptor and the brain
center, your brain will locate the stimulus
where receptors are (e.g. phantom limb)
• reorganization of brain map in somatosensory
cortex
• Some believe it can be blocked by local
anesthetics in spinal cord.
• A phantom limb is the sensation that an amputated
or missing limb is still attached to the body.
• Approximately 60 to 80% of individuals with an
amputation experience phantom sensations in their
amputated limb, and the majority of the sensations
are painful.
• Phantom sensations may also occur after the
removal of body parts e.g. after amputation of the
breast, extraction of a tooth (phantom tooth pain)
or removal of an eye (phantom eye syndrome)
DALE’S LAW
• At one type of synapse only one type of
neurotransmitter is released
TRANSDUCTION OF SENSORY
STIMULI INTO RECEPTOR POTENTIAL
AND NERVE IMPULSESReceptor Potentials
When pressure is
applied to
pacinian corpuscle
, a small non-
propogated
depolarizing
potential develops
called receptor
potential.
PROPERTIES OF RECEPTOR
POTENTIAL
• It is graded potential
• It is non- propagated
• It doesn't obey all or none law
MECHANISMS OF RECEPTOR
POTENTIALS.
• Different receptors can be excited in one of several ways to cause receptor potentials:
• (1) by mechanical deformation of the receptor, which stretches the receptor
membrane and opens ion channels;
• (2) by application of a chemical to the membrane, which also opens ion channels;
• (3) by change of the temperature of the membrane, which
alters the permeability of the membrane; or
• (4) by the effects of electromagnetic radiation,
RELATION OF THE RECEPTOR
POTENTIAL TO ACTION POTENTIALS
• When the receptor potential rises above the
threshold for eliciting action potentials in the nerve
fiber attached to the receptor, then action potentials
occur.
• More the receptor potential rises above the
threshold level, the greater becomes the action
potential frequency.
RELATION OF THE RECEPTOR
POTENTIAL TO ACTION POTENTIALS
• More the receptor
potential rises above
the threshold level,
the greater becomes
the action potential
frequency.
RELATION BETWEEN STIMULUS
INTENSITY AND THE RECEPTOR
POTENTIAL.
• Amplitude increases
rapidly and then less
rapid rise at high stimulus
strength
• the frequency of
repetitive action
potentials transmitted
from sensory receptors
also increase
• But very strong
stimulation decrease
action potentials as well
ADAPTATION OF RECEPTORS
• Another characteristic of all
sensory receptors is that they
adapt either partially or
completely to any constant
stimulus after a period of time.
• That is, when a continuous
sensory stimulus is applied, the
receptor responds at a high
impulse rate at first and then at a
progressively slower rate until
finally the rate of action potentials
decreases to very few or often to
none at all.
MECHANISMS BY WHICH RECEPTORS
ADAPT
• part of the adaptation results from
readjustments in the structure of the receptor
itself,
• and part from an electrical type of
accommodation in the terminal nerve fibril
SLOWLY AND RAPIDLY
ADAPTING RECEPTORS
• Slowly Adapting Receptors Detect
Continuous Stimulus Strength—The
“Tonic” Receptors.
• impulses from the muscle spindles and
Golgi tendon apparatuses allow the
nervous system to know the status of
muscle contraction
• Receptors of the macula in the
vestibular apparatuses
• pain receptors
• baroreceptors of the arterial tree
• chemoreceptors of the carotid and
aortic bodies.
• Rapidly Adapting Receptors Detect
Change in Stimulus Strength—The “Rate
Receptors,” “Movement Receptors,” or
“Phasic Receptors.”
• Pacinian and meissner’s
• Importance of the Rate Receptors—
Their Predictive Function.
TYPES OF NERVE FIBERS
• To classify nerve fibers
• To understand the properties and differences
of nerve fibers
NERVE FIBERS THAT TRANSMIT
DIFFERENT TYPES OF SIGNALS, AND
THEIR PHYSIOLOGIC
CLASSIFICATION
nerve fibers come in all sizes between 0.5
and 20 micrometers in diameter—
the larger the diameter, the greater the conducting
velocity
The range of conducting velocities is between 0.5
and 120 m/sec
GENERAL CLASSIFICATION
OF NERVE FIBERS
In the general classification, the fibers are divided into types
• A, B and C,
• A&B are myelinated. C fibers are not
• the type A fibers are further subdivided into
• A α (annulospiral endings)
• A β (touch and pressure)
• A ɣ (motor to muscle spindles)
• Aδ (Pain and temp)
• B fibers are pre-ganglionic fibers
• C fibers are post ganglionic and also transmit slow pain
ALTERNATIVE CLASSIFICATION
USED BY SENSORY
PHYSIOLOGISTS
• Group Ia
Muscle spindle
• Group Ib
Golgi tendon organs
• Group II
Cutaneous tactile receptors
• Group III
Fibers carrying temperature, crude touch, and pricking pain sensations
• Group IV
Un-myelinated fibers carrying pain, itch, temperature, and crude touch
sensations
Diameter in
micrometers
Conduction
velocity in
m/sec
Motor Fiber Type
Aα 0.12-20 0.72-120 Extrafusal
skeletal muscle
fibers
Aγ 0.12-8.2 0.12-48 Intrafusal muscle
fibers
B 0.21-33 0.86-18 Preganglionic
autonomic fibers
C 0.2-2 0.5-2 Postganglionic
autonomic fibers
Peripheral nerve
fibers
Afferents Diameter of
nerve fibers in
mm
Conduction
velocity in m/sec
Receptors
Sensory Fiber Type
Aα Ia and Ib 0.13-20 0.80-120 m/sec Primary muscle
spindles, Golgi
tendon organ
Aβ II 0.16-12 0.35-75 Secondary muscle
spindles, skin
mechanoreceptors
Aδ III 0.11-5 0.15-30 Skin
mechanoreceptors,
thermal receptors,
fast pain
C IV 0.2-1.5 0.5-2 Slow pain and temp
DIVERGING PATHWAYS
Two types of divergence
• Amplifying type in same direction
• Divergence into multiple tracts to enter
multiple areas of brain
CONVERGING PATHWAYS
CONVERGENCE OF SIGNALS
• Convergence means signals from multiple inputs uniting
to excite a single neuron.
• Convergence from a single source. That is, multiple
terminals from a single incoming fiber tract terminate
on the same neuron.
• Convergence can also result from input signals
(excitatory or inhibitory) from multiple sources
SOMATIC SENSATIONS
AND MECHANICAL
RECEPTORS
DR. SADIA NAZIR
ASSISTANT PROFESSOR PHYSIOLOGY
LMDC
• Classify somatic sensations
• Classify mechanical receptors
Classification of Sensations
• The somatic senses are the nervous mechanisms
that collect sensory information from all over the
body.
• Special senses, which mean specifically vision,
hearing, smell, taste and equilibrium.
CLASSIFICATION OF SOMATIC
SENSES
• The mechanoreceptive somatic senses,
which include both tactile and position
sensations.
• The thermoreceptive senses, which detect
heat and cold
• The pain sense, which is activated by any
factor that damages the tissues.
MECHANORECEPTIVE SOMATIC
SENSES
• The tactile senses include touch, pressure,
vibration, and tickle
• the position senses include static position and rate
of movement
DETECTION AND TRANSMISSION OF
TACTILE SENSATIONS
• Touch, pressure, and vibration are all
detected by the same types of receptors
called tactile receptors.
• There are at least six entirely different
types of tactile receptors
FREE NERVE ENDINGS
• Free nerve endings,
which are found
everywhere in the
skin and in many
other tissues, can
• detect touch and
pressure
MEISSNER’S CORPUSCLE
• Elongated encapsulated nerve
ending of a large (type AB)
myelinated nerve fiber.
• Inside the capsulation are
many branching terminal
nerve filaments.
• These corpuscles are present
in the non hairy parts of the
skin .
• Meissner’s corpuscles adapt in
a fraction of a second after
they are stimulated,
• Detect low frequency
vibration.
MERKEL’S DISCS
• The hairy parts and non
hairy part of the skin also
contain moderate numbers
of expanded tip receptors
• they transmit an initially
strong but partially
adapting signal and then a
continuing weaker signal
• adapts only slowly.
• Therefore, they are
responsible for giving
steady-state signals
IGGO DOME RECEPTOR
• Merkel’s discs are
often grouped
together in a receptor
organ called the Iggo
dome receptor, which
projects upward
against the underside
of the epithelium of
the skin
HAIR END-ORGAN
• This receptor adapts
readily and, like
Meissner’s corpuscles,
detects mainly
• (a) movement of
objects on the surface
of the body or
• (b) initial contact with
the body.
RUFFINI’S END-ORGANS
• Multibranched,
encapsulated endings,
• These endings adapt
very slowly
• They are also found in
joint capsules and help
to signal the degree of
joint rotation
• Found in skin and
deeper tissues
PACINIAN CORPUSCLES
• Lie both immediately
beneath the skin and deep
in the fascial tissues of the
body.
• They are stimulated only by
rapid local compression of
the tissues because they
adapt in a few hundredths
of a second.
• Important for detecting
tissue vibration or other
rapid changes in the
mechanical state of the
tissues.
• Position sense
1. Static
2. Rate of movement called kinesthesia
• Receptors
1. Muscle spindles
2. Golgi tendon organs
3. Ruffni’s endings
4. Pacinian
• Texture meissner & merkel
• Localization meissner & merkel
• Discrimination meissner
• Vibration meissner & pacinian
• Prolonged touch merkel’s
• Prolonged deep touch & pressure
ruffni’s
TRANSMISSION OF TACTILE SIGNALS
IN PERIPHERAL NERVE FIBERS
• Transmit their signals in type A-beta nerve fibers
that have transmission velocities ranging from 30
to 70 m/sec.
• free nerve ending tactile receptors transmit signals
mainly by way of the small type A-delta myelinated
fibers that conduct at velocities of only 5 to 30
m/sec.
• Some tactile free nerve endings transmit by way of
type C unmyelinated fibers (up to 2 m/sec;) these
send signals into the spinal cord and lower brain
stem, mainly the sensation of tickle.
DETECTION OF VIBRATION
• Pacinian corpuscles can detect signal
vibrations from 30 to 800 cycles per second
and they also transmit their signals over type
A-beta nerve fibers.
• Meissner’s corpuscles detect vibrations from 2
to 80 cycles per seconds
TICKLE AND ITCH
• rapidly adapting mechanoreceptive free nerve
endings elicit only the tickle and itch
sensations.
• These sensations are transmitted by very small
type C, unmyelinated fibers similar to those
that transmit the aching, slow type of pain.
• Receptors afferents
dorsal root ganglia gray column
ascending tracts thalamus
sensory cortex
SENSORY PATHWAYS
• Dorsal Column-medial lemsiscus pathway
• Sensations carried:
• Light touch
• pressure
• Tactile localisation
• 2 point discrimination
• Flutter and vibration
• Stereognosis
• Propioception
• Graphesthesia
• Large myleinated nerve fibres (fast)
• Spatial orientation
•DORSAL COLUMN MEDIAL
LEMNISCUS PATHWAY
•Nerve fibres enters through
dorsal roots divides into
medial +lateral barnches
•Medial ascends in dorsal
columns
•Lateral further branches
and synapse with local
neurons
•Some fibres are given
off to the dorsal column
•Some form local
reflexes
•Others form
•Ascending fibres terminate on cuneate and gracile nuclei
•Decussate to the opposite side immediately medial
lemniscus
•Fibers terminate in the thalamic sensory relay area, called
the ventrobasal complex.
•third-order nerve fibers project, mainly to
• the postcentral gyrus of the cerebral cortex, (called somatic
sensory area I)
•also project to a smaller area in the lateral parietal cortex
called somatic sensory area II).
• the fibers from the lower parts
of the body lie toward the
center of the cord, whereas
new fibres enter laterally.
• In the thalamus, the tail end of
the body represented by the
most lateral portions of the
ventrobasal complex and the
head and face represented by
medial areas of the complex.
• because of the crossing of the
medial lemnisci in the medulla,
the left side of the body is
represented in the right side of
the thalamus, and the right
side of the body in the left
side of the thalamus.
Spatial Orientation
ANTEROLATERAL SYSTEM
Transmits sensory signals that DO NOT require highly
discrete localization
• Composed of smaller, myelinated nerve fibers
(transmission speeds 40 m/sec)
• Less spatial orientation
• Sensory modalities – wide range
• Comprise of:
• Anterior spinothalamic tract
• Lateral spinothalamic tract
ANTEROLATERAL SYSTEM
• Pain
• Thermal sensations
(including warmth & cold)
• Crude touch and pressure
sensations
• Tickle and itch sensations
• Sexual sensations
•From receptors (free nerve
ending enter dorsal horn
(cell bodies of these first
order neurons are in the
dorsal root ganglion)
•Synapse with 2nd order
within 1-2 segments
•Second order neurons
dorsal horn (at all levels).
Their axons decussate in the
anterior white and gray
commisure
•Joined by trigeminothalmic
fibers in medulla, send
collaterals to reticular
formation (alertness to pain)
•3rd order neurons VPL
nucleus of thalamus. Their
fibres ascend through the
posterior limb of internal
capsule corona radiate
•4th order neurons of the
cerebral cortex (Broadmans
areas 3,1.2
Somatosensory cortex)
•Some fibers from the
second order neuron
decussate and ascend as
anterior spinothalmic tract
•Both anterior & lateral
spinothalamic tracts unite
in MO forming spinal
lemniscus
ANTERIOR AND
LATERAL
SPINOTHALMIC
TRACTS
Some fibers carrying crude
touch, tickle may ascend 8-10
spinal cord segments before
synapsing with secondary
neurons. Ascend more
anteriorly as the anterior
spinothalmic tract
Secondary fibers decussate in
anterior gray or white
commissures. Acend to the
medulla together spinal
lemniscus
• Dorsal Column–Medial
Lemniscal System
• 1. Touch sensations
requiring a high degree of
localization of the stimulus
• 2. Touch sensations
requiring transmission of
fine gradations of intensity
• 3. Phasic sensations, such as
vibratory sensations
• 4. Sensations that signal
movement against the skin
• 5. Position sensations from
the joints
• 6. Pressure sensations
having to do with fine
degrees of judgment of
pressure intensity
• Anterolateral System
• 1. Pain
• 2. Thermal sensations,
including both warmth and
cold sensations
• 3. Crude touch and pressure
sensations capable only of
crude localizing ability on
the surface of the body
• 4. Tickle and itch sensations
• 5. Sexual sensations
Cortex: Broadmann’s
areas (50)
Central fissure: anterior
to it motor cortex
Posterior sensory
cortex
Occipital lobe visual
Tempral Lobe Auditory
SS1 and SS2
Located  aneterior part
of parietal lobe
SS1-high degree of
localization
Molecular layer
External granular layer
External pyramidal layer
Internal granular layer
Internal pyramidal layer
Polymorphic layer
FUNCTIONS OF
SOMATOSENSORY AREA I
• Localize and discriminate
discretely the different
sensations in the different
parts of the body
• judge critical degrees of
pressure against the body
• judge the texture,
BILATERAL EXCISION OF
SOMATOSENSORY AREA
Pt is unable to
• Localize and discriminate discretely the
different sensations in the different parts of the
body
• judge critical degrees of pressure against the
body
• judge the texture, weights, shapes or forms of
objects. This is called astereognosis.
• Judge the shape by drawing. Agraphaesthesia
Effect of Removing the Somatosensory Association
Area—(5,7) Amorphosynthesis
• The person loses ability to recognize
complex objects and complex forms felt on
the opposite side of the body.
• He or she loses most of the sense of form of
his or her own body parts on the opposite
side and forgets that it is there .
• When feeling objects, the person tends to
recognize only one side of the object and
forgets that the other side even exists.
LESIONS OF DORSAL COLUMN
TRACT
• Sensory ataxia
• Loss of vibration
• Loss of tactile discrimination
• Loss of tactile localization
• Dorsal Column–Medial
Lemniscal System
• Touch sensations requiring a
high degree of localization of
the stimulus
• Touch sensations requiring
transmission of fine
gradations of intensity
• Phasic sensations, such as
vibratory sensations
• Sensations that signal
movement against the skin
• Position sensations from the
joints
• Pressure sensations having to
do with fine degrees of
judgment of pressure intensity
• Anterolateral System
• Pain
• Thermal sensations, including
both warmth and
cold sensations
• Crude touch and pressure
sensations capable only of
crude localizing ability on the
surface of the body
• Tickle and itch sensations
• Sexual sensations
• Dermatome
Segment of skin supplied by the spinal nerve
PAIN AND
ANALGESIA SYSTEM
DR. SADIA NAZIR
ASSISTANT PROFESSOR PHYSIOLOGY
LMDC
PAIN IS A PROTECTIVE
MECHANISM
• Pain occurs whenever any tissues are being
damaged, and it causes the individual to react
to remove the pain stimulus.
TYPES OF PAIN
• Fast Pain
• Slow Pain
• Fast pain is felt within about 0.1 second after a
pain stimulus is applied
• Slow pain begins after 1 second or more and then
increases slowly over many seconds and
sometimes even minutes.
QUALITIES OF PAIN
• Fast pain is also described by many alternative
names, such as sharp pain, pricking pain,
acute pain, and electric pain
• Slow pain also goes by many names, such as
slow burning pain, aching pain, throbbing
pain, nauseous pain, and chronic pain
PAIN RECEPTORS
• Are Free Nerve Endings
• They are widespread in the superficial layers of
the skin as well as in certain internal tissues,
such as the periosteum, the arterial walls, the
joint surfaces, and the falx and tentorium in
the cranial vault.
• Non-adapting Nature of Pain Receptors
Three Types of Stimuli Excite Pain Receptors—
• Mechanical
• Thermal
• Chemical
• Some of the chemicals that excite the chemical
type of pain are bradykinin, serotonin,
histamine, potassium ions, acids,
acetylcholine, and proteolytic enzymes
• In addition, prostaglandins and substance P
enhance the sensitivity of pain endings but do
not directly excite them
DUAL PATHWAYS FOR
TRANSMISSION OF PAIN SIGNALS
INTO THE CENTRAL NERVOUS
SYSTEM
• Peripheral Pain Fibers—
• “Fast” (A delta) and “Slow” Fibers (C fibers)
• The two pathways mainly correspond to the two
types of pain—
• a fast-sharp pain pathway and
• a slow-chronic pain pathway.
DUAL PATHWAYS FOR TRANSMISSION OF
PAIN SIGNALS INTO THE CENTRAL
NERVOUS SYSTEM
FAST PAIN
(NEOSPINOTHALAMIC
PATHWAY)
1. Mechanical or thermal pain
stimuli
2. A delta fibers at velocities
between 6 and 30 m/sec.
3. They terminate mainly in
lamina I (lamina
marginalis)
SLOW PAIN
(PALEOSPINOTHALAMIC
PATHWAY)
1. Mostly by chemical types
of pain stimuli but
sometimes by persisting
mechanical or thermal
stimuli.
2. C fibers at velocities
between 0.5 and 2 m/sec.
3. laminae II and III of the
dorsal horns, which
together are called the
substantia gelatinosa,
Fast pain
4. most pass all the way to the
thalamus (Ventrobasal)
• Project to somatosensory cortex.
5. can be localized much more
exactly in the different parts of
the body than can slow-chronic
pain.
6. Glutamate, the Probable
Neurotransmitter of the Fast
Pain Fibers
SLOW PAIN
4.most terminate in one of
three areas:
(a) reticular nuclei
(b) tectal area of the
mesencephalon
(c) periaqueductal gray region
(d) Intralaminar nuclei and
hypothalamus
5.Poorly localized.
6.Type C pain fiber terminals
entering the spinal cord
Pain Suppression (“Analgesia”) System in the Brain
and Spinal Cord
• Inhibition of pain signals at spinal cord by
descending brain fibers
• Encephalin secreting neurons in cord and brain stem
• Inhibition of pain fibers by tactile incoming fibers
Acupuncture analgesia (AA)
• technique of relieving pain by
inserting and manipulating
threadlike needles at key points
• acupuncture endorphin hypothesis
• Acupuncture needles activate
specific afferent nerve
fibersCNSblocking pain
transmission at both
• the spinal-cord and brain levels
through use of endorphins and
closely related endogenous opiates.
• The periaqueductal gray and periventricular
areas of the mesencephalon and upper pons
surround the aqueduct of Sylvius and portions
of the third and fourth ventricles. Neurons from
these areas send signals to
• The raphe magnus nucleus, a thin midline
nucleus located in the lower pons and upper
medulla, and the nucleus reticularis
paragigantocellularis, located laterally in the
medulla. From these nuclei, second-order
signals are transmitted down the dorsolateral
columns in the spinal cord to
• Pain inhibitory complex located in the dorsal
horns of the spinal cord.
INHIBITION OF PAIN TRANSMISSION BY
SIMULTANEOUS TACTILE SENSORY
SIGNALS
• Stimulation of large type A beta sensory fibers
from peripheral tactile receptors can depress
transmission of pain signals from the same body
area.
• This presumably results from local lateral
inhibition in
the spinal cord.
• It explains why such simple maneuvers as rubbing
the skin near painful areas is often effective in
relieving pain.
• It also explains why liniments are often useful for
pain relief.
• Allodynia
Non painful stimulus causes pain (Lesion of VPL of
thalamus)
• Hyperalgesia
Hypersensitivity to pain
A pain nervous pathway sometimes becomes excessively
excitable;.
• Possible causes of hyperalgesia are
• Excessive sensitivity of the pain receptors themselves,
which is called primary hyperalgesia (Burns)
REFERRED PAIN
• Often a person feels pain in a part of the body
that is fairly remote from the tissue causing
the pain. This is called referred pain. For
instance, pain in one of the visceral organs
often is referred to an area on the body
surface.
• Referred Pain
MECHANISM OF REFERRED PAIN.
VISCERAL PAIN AND SURFACE
PAIN
VISCERAL PAIN
• Highly localized types of
damage to the viscera seldom
cause severe pain.
• True visceral pain is
transmitted via pain sensory
fibers within the autonomic
nerve bundles, and the
sensations are referred to
surface areas of the body
often far from the painful
organ.
SURFACE
PAIN/PARIETAL PAIN
• Parietal sensations are
conducted directly into
local spinal nerves from
the parietal
peritoneum, pleura, or
pericardium, and these
sensations are usually
localized over painful
area.
VISCERAL” AND THE “PARIETAL”
PAIN
TRANSMISSION PATHWAYS
CAUSES OF TRUE VISCERAL PAIN
• Any stimulus that excites pain nerve endings in diffuse areas of the viscera
can cause visceral pain.
• Such stimuli include
• ischemia of visceral tissue,
• chemical damage to the surfaces of the viscera,
• spasm of the smooth muscle of a hollow viscus,
• excess distention of a hollow viscus, and stretching of the connective
tissue surrounding or within the viscus.
• Essentially all visceral pain that originates in the thoracic and abdominal
cavities is transmitted through small type C pain fibers and, therefore, can
transmit only the chronic-aching-suffering type of pain.
Hyperalgesia
• A pain nervous pathway sometimes becomes
excessively excitable; this gives rise to hyperalgesia,
which means hypersensitivity to pain.
• Possible causes of hyperalgesia are
• (1) excessive sensitivity of the pain receptors
themselves, which is called primary hyperalgesia
• (2) facilitation of sensory transmission, which is
called secondary hyperalgesia.
• Herpes Zoster (Shingles)
• Herpesvirus infects a dorsal root ganglion.
• This causes severe pain in the dermatomal segment
served by the ganglion, thus eliciting a segmental
type of pain that circles halfway around the body.
• The disease is called herpes zoster, or “shingles,”
because of a skin eruption that often ensues.
• Tic Douloureux
• Lancinating pain occasionally occurs in some people
over one side of the face in the sensory distribution
area (or part of the area) of the fifth or ninth nerves;
This phenomenon is called tic douloureux
(trigeminal neuralgia or glossopharyngeal
neuralgia).
• The pain feels like sudden electrical shocks, and it
may appear for only a few seconds at a time or may
be almost continuous.
• Headache
• Headaches are a type of pain referred to the surface
of the head from deep head structures.
• Pain-Sensitive Areas in Cranial Vault.
• Tugging on the venous sinuses around the brain,
• Damaging the tentorium,
• Stretching the dura at the base of the brain can
cause intense pain that is recognized as headache
• Middle meningeal artery is a pain sensitive structure
TYPES OF INTRACRANIAL
HEADACHE
• Brain tumors
• Headache of Meningitis.
• Headache Caused by
Low Cerebrospinal Fluid
Pressure.
• Migraine Headache
• Alcoholic Headache
TYPES OF EXTRACRANIAL
HEADACHE
• Headache Resulting
from Muscle Spasm.
• Headache Caused by
Irritation of Nasal and
Accessory Nasal
Structures.
• Headache Caused by
Eye Disorders
THERMAL SENSATIONS
• The human being can perceive different gradations of
cold and heat,
• from freezing cold
• cold
• cool
• Indifferent
• to warm
• hot
• burning hot.
• Thermal gradations are discriminated by at
least three types of sensory receptors:
• cold receptors,
• warmth receptors,
• and pain receptors.
BROWN-SÉQUARD SYNDROME
• If the spinal cord is transected on only one side, the Brown-Séquard syndrome occurs.
• All motor functions are blocked on the side of the transection in all segments below
the level of the transection and at the level.
• The sensations of pain, heat, and cold— sensations served by the spinothalamic
pathway—are lost on the opposite side of the body in all dermatomes two to six
segments below the level of the transection.
• The dorsal and dorsolateral columns—kinesthetic and position sensations, vibration
sensation, discrete localization, and two-point discrimination—are lost on the side of
the transection in all dermatomes below the level of the transection.
BROWN-SÉQUARD SYNDROME
At the level Below the
level
Above the
level
LMN paralysis same side UMN paralysis same
side
Cutaneous anesthesia in
the dermatomal
segment of ipsilateral
side
Loss of pain and temp
of contralateral side 2
to 5 segments below
the level of lesion
Altered sensations
Loss of vibration, fine
touch, tactile
localization and
discrimination in all
Receptors
Receptors

More Related Content

What's hot

Receptor
ReceptorReceptor
Receptor
Sado Anatomist
 
Physiology of sensory systems
Physiology of sensory systemsPhysiology of sensory systems
Physiology of sensory systems
Serge Eddy Mba
 
Sensory Physiology
Sensory PhysiologySensory Physiology
Sensory Physiologyraj kumar
 
RESTING MEMBRANE POTENTIAL & ACTION POTENTIAL
RESTING MEMBRANE POTENTIAL & ACTION POTENTIALRESTING MEMBRANE POTENTIAL & ACTION POTENTIAL
RESTING MEMBRANE POTENTIAL & ACTION POTENTIAL
Nabeel Beeran Abdul Rahiman
 
Receptors properties
Receptors propertiesReceptors properties
Receptors properties
Dr Sara Sadiq
 
Y2 s1 sensory system
Y2 s1 sensory systemY2 s1 sensory system
Y2 s1 sensory systemvajira54
 
The synapse
The synapseThe synapse
The synapse
presh_g
 
Properties of receptors
Properties of receptorsProperties of receptors
Properties of receptors
Nadha Abubacker
 
Properties of reflexes
Properties of reflexesProperties of reflexes
Properties of reflexes
Dr Nilesh Kate
 
Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...
Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...
Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...Rajesh Goit
 
Classification of Sensory receptor 1
Classification of Sensory receptor 1Classification of Sensory receptor 1
Classification of Sensory receptor 1
Surjya Kumar Saikia
 
Inhibition of the central nervous system
Inhibition of the central nervous systemInhibition of the central nervous system
Inhibition of the central nervous system
Gustavo Duarte Viana
 
The neuromuscular physiology
The neuromuscular physiologyThe neuromuscular physiology
The neuromuscular physiology
Sourav Mondal
 
Synapses
SynapsesSynapses
Synapses
M Sohail Raza
 
Synapse by sunita tiwale
Synapse by sunita tiwale  Synapse by sunita tiwale
Synapse by sunita tiwale
Physiology Dept
 
Physiology of the Neuromuscular Junction
Physiology of the Neuromuscular JunctionPhysiology of the Neuromuscular Junction
Physiology of the Neuromuscular Junction
Ashwin Haridas
 
General Physiology - The nervous system, basic functions of synapses
General Physiology - The nervous system, basic functions of synapsesGeneral Physiology - The nervous system, basic functions of synapses
General Physiology - The nervous system, basic functions of synapses
Hamzeh AlBattikhi
 
Sensory system receptors.hussein f.sakr
Sensory system receptors.hussein f.sakrSensory system receptors.hussein f.sakr
Sensory system receptors.hussein f.sakr
Hussein Sakr
 

What's hot (20)

Receptor
ReceptorReceptor
Receptor
 
Physiology of sensory systems
Physiology of sensory systemsPhysiology of sensory systems
Physiology of sensory systems
 
Sensory Physiology
Sensory PhysiologySensory Physiology
Sensory Physiology
 
RESTING MEMBRANE POTENTIAL & ACTION POTENTIAL
RESTING MEMBRANE POTENTIAL & ACTION POTENTIALRESTING MEMBRANE POTENTIAL & ACTION POTENTIAL
RESTING MEMBRANE POTENTIAL & ACTION POTENTIAL
 
Receptors properties
Receptors propertiesReceptors properties
Receptors properties
 
Synapse
SynapseSynapse
Synapse
 
Y2 s1 sensory system
Y2 s1 sensory systemY2 s1 sensory system
Y2 s1 sensory system
 
The synapse
The synapseThe synapse
The synapse
 
Properties of receptors
Properties of receptorsProperties of receptors
Properties of receptors
 
Properties of reflexes
Properties of reflexesProperties of reflexes
Properties of reflexes
 
Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...
Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...
Origin and spread of cardiac impulse, pacemaker, conducting system of heart, ...
 
Classification of Sensory receptor 1
Classification of Sensory receptor 1Classification of Sensory receptor 1
Classification of Sensory receptor 1
 
Inhibition of the central nervous system
Inhibition of the central nervous systemInhibition of the central nervous system
Inhibition of the central nervous system
 
The neuromuscular physiology
The neuromuscular physiologyThe neuromuscular physiology
The neuromuscular physiology
 
Synapses
SynapsesSynapses
Synapses
 
Synapse by sunita tiwale
Synapse by sunita tiwale  Synapse by sunita tiwale
Synapse by sunita tiwale
 
Physiology of the Neuromuscular Junction
Physiology of the Neuromuscular JunctionPhysiology of the Neuromuscular Junction
Physiology of the Neuromuscular Junction
 
ASCENDING TRACTS
ASCENDING TRACTSASCENDING TRACTS
ASCENDING TRACTS
 
General Physiology - The nervous system, basic functions of synapses
General Physiology - The nervous system, basic functions of synapsesGeneral Physiology - The nervous system, basic functions of synapses
General Physiology - The nervous system, basic functions of synapses
 
Sensory system receptors.hussein f.sakr
Sensory system receptors.hussein f.sakrSensory system receptors.hussein f.sakr
Sensory system receptors.hussein f.sakr
 

Similar to Receptors

Sensory Receptors 2023 (2).pdf
Sensory Receptors 2023 (2).pdfSensory Receptors 2023 (2).pdf
Sensory Receptors 2023 (2).pdf
Anaaya Batool
 
physiology of Sensory nervous system, updated 2021
physiology of Sensory nervous system,  updated 2021physiology of Sensory nervous system,  updated 2021
physiology of Sensory nervous system, updated 2021
dina merzeban
 
PY3.2 Describe the types, functions & properties of nerve fiber.pptx
PY3.2 Describe the types, functions & properties of nerve fiber.pptxPY3.2 Describe the types, functions & properties of nerve fiber.pptx
PY3.2 Describe the types, functions & properties of nerve fiber.pptx
Shikha Saxena
 
Sensory system review
Sensory system reviewSensory system review
Sensory system review
dina merzeban
 
Sensory systems 1
Sensory systems 1Sensory systems 1
Sensory systems 1whisper119
 
PAIN AND PAIN PATHWAYS
PAIN AND PAIN PATHWAYSPAIN AND PAIN PATHWAYS
PAIN AND PAIN PATHWAYS
HaripriyaRajaram
 
NERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptx
NERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptxNERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptx
NERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptx
Sangita Sarma
 
Receptors 21.06.2023 physiology CNS-1.pptx
Receptors 21.06.2023 physiology CNS-1.pptxReceptors 21.06.2023 physiology CNS-1.pptx
Receptors 21.06.2023 physiology CNS-1.pptx
Drratnakumari
 
1 neural control of exercising muscle
1 neural control of exercising muscle1 neural control of exercising muscle
1 neural control of exercising muscle
ARNABJAN DAS
 
PERIPHERAL NERVES.pptx
PERIPHERAL NERVES.pptxPERIPHERAL NERVES.pptx
PERIPHERAL NERVES.pptx
NainaJoshi9
 
Neurophysiology lecture
Neurophysiology lectureNeurophysiology lecture
Neurophysiology lecture
RASHA
 
Neurophysiology lecture
Neurophysiology lectureNeurophysiology lecture
Neurophysiology lecture
RASHA
 
2nd year small group discussion Synapse and sensory receptors.pptx
2nd year small group discussion Synapse and sensory receptors.pptx2nd year small group discussion Synapse and sensory receptors.pptx
2nd year small group discussion Synapse and sensory receptors.pptx
bobehe4189
 
Ch 13 lecture_outline_a
Ch 13 lecture_outline_aCh 13 lecture_outline_a
Ch 13 lecture_outline_aTheSlaps
 
Ch 13 lecture_outline_a
Ch 13 lecture_outline_aCh 13 lecture_outline_a
Ch 13 lecture_outline_aTheSlaps
 
NEURAL TRANSMISSION ppt
NEURAL TRANSMISSION pptNEURAL TRANSMISSION ppt
NEURAL TRANSMISSION ppt
NiveditaMenonC
 
Synaptic transmission
Synaptic transmissionSynaptic transmission
Synaptic transmission
GullAZahra
 
pain and pain pathways
pain and pain pathwayspain and pain pathways
pain and pain pathways
DrShrawani Chouhan
 
Basic overview of nerve conduction studies
Basic overview of nerve conduction studiesBasic overview of nerve conduction studies
Basic overview of nerve conduction studies
Abdul Ali
 

Similar to Receptors (20)

Sensory Receptors 2023 (2).pdf
Sensory Receptors 2023 (2).pdfSensory Receptors 2023 (2).pdf
Sensory Receptors 2023 (2).pdf
 
physiology of Sensory nervous system, updated 2021
physiology of Sensory nervous system,  updated 2021physiology of Sensory nervous system,  updated 2021
physiology of Sensory nervous system, updated 2021
 
PY3.2 Describe the types, functions & properties of nerve fiber.pptx
PY3.2 Describe the types, functions & properties of nerve fiber.pptxPY3.2 Describe the types, functions & properties of nerve fiber.pptx
PY3.2 Describe the types, functions & properties of nerve fiber.pptx
 
Sensory system review
Sensory system reviewSensory system review
Sensory system review
 
Sensory systems 1
Sensory systems 1Sensory systems 1
Sensory systems 1
 
PAIN AND PAIN PATHWAYS
PAIN AND PAIN PATHWAYSPAIN AND PAIN PATHWAYS
PAIN AND PAIN PATHWAYS
 
NERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptx
NERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptxNERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptx
NERVE FIBRES, RECEPTORS & NEUROTRANSMITTERS.pptx
 
Receptors 21.06.2023 physiology CNS-1.pptx
Receptors 21.06.2023 physiology CNS-1.pptxReceptors 21.06.2023 physiology CNS-1.pptx
Receptors 21.06.2023 physiology CNS-1.pptx
 
1 neural control of exercising muscle
1 neural control of exercising muscle1 neural control of exercising muscle
1 neural control of exercising muscle
 
PERIPHERAL NERVES.pptx
PERIPHERAL NERVES.pptxPERIPHERAL NERVES.pptx
PERIPHERAL NERVES.pptx
 
Neurophysiology lecture
Neurophysiology lectureNeurophysiology lecture
Neurophysiology lecture
 
Neurophysiology lecture
Neurophysiology lectureNeurophysiology lecture
Neurophysiology lecture
 
2nd year small group discussion Synapse and sensory receptors.pptx
2nd year small group discussion Synapse and sensory receptors.pptx2nd year small group discussion Synapse and sensory receptors.pptx
2nd year small group discussion Synapse and sensory receptors.pptx
 
Ch 13 lecture_outline_a
Ch 13 lecture_outline_aCh 13 lecture_outline_a
Ch 13 lecture_outline_a
 
Ch 13 lecture_outline_a
Ch 13 lecture_outline_aCh 13 lecture_outline_a
Ch 13 lecture_outline_a
 
NEURAL TRANSMISSION ppt
NEURAL TRANSMISSION pptNEURAL TRANSMISSION ppt
NEURAL TRANSMISSION ppt
 
Synaptic transmission
Synaptic transmissionSynaptic transmission
Synaptic transmission
 
Nervous system
Nervous systemNervous system
Nervous system
 
pain and pain pathways
pain and pain pathwayspain and pain pathways
pain and pain pathways
 
Basic overview of nerve conduction studies
Basic overview of nerve conduction studiesBasic overview of nerve conduction studies
Basic overview of nerve conduction studies
 

More from bigboss716

Autonomic nervous system pharmacology
Autonomic nervous system pharmacologyAutonomic nervous system pharmacology
Autonomic nervous system pharmacology
bigboss716
 
Pronator muscles anatomy and strengthening
Pronator muscles anatomy and strengtheningPronator muscles anatomy and strengthening
Pronator muscles anatomy and strengthening
bigboss716
 
suspension therapy and usage
   suspension therapy and usage   suspension therapy and usage
suspension therapy and usage
bigboss716
 
kinesiology basics
kinesiology basicskinesiology basics
kinesiology basics
bigboss716
 
Embryology limb defects
Embryology  limb defectsEmbryology  limb defects
Embryology limb defects
bigboss716
 
Twins (embryology)
Twins (embryology)Twins (embryology)
Twins (embryology)
bigboss716
 
lower limb anatomy MCQs
 lower limb anatomy MCQs lower limb anatomy MCQs
lower limb anatomy MCQs
bigboss716
 
Vision disorder
Vision disorderVision disorder
Vision disorder
bigboss716
 
Tens transcutaneous electrical nerve stimulator
Tens  transcutaneous electrical nerve stimulatorTens  transcutaneous electrical nerve stimulator
Tens transcutaneous electrical nerve stimulator
bigboss716
 
Pharmaco dyanamics studies
Pharmaco dyanamics studies Pharmaco dyanamics studies
Pharmaco dyanamics studies
bigboss716
 
Renin angiotensin system
Renin angiotensin systemRenin angiotensin system
Renin angiotensin system
bigboss716
 
Directly acting vasodilators
Directly acting vasodilatorsDirectly acting vasodilators
Directly acting vasodilators
bigboss716
 
Antihypertensives
Antihypertensives Antihypertensives
Antihypertensives
bigboss716
 
Bone pathology
Bone pathologyBone pathology
Bone pathology
bigboss716
 
The limbic system and the hypothalamus
The limbic system and the hypothalamusThe limbic system and the hypothalamus
The limbic system and the hypothalamus
bigboss716
 
Vestibular apparatus
Vestibular apparatusVestibular apparatus
Vestibular apparatus
bigboss716
 
Hypothalmus& thalmus
Hypothalmus& thalmusHypothalmus& thalmus
Hypothalmus& thalmus
bigboss716
 
Cerebral cortex
Cerebral cortexCerebral cortex
Cerebral cortex
bigboss716
 
Cerebral blood flow
Cerebral blood flowCerebral blood flow
Cerebral blood flow
bigboss716
 
Cerebellum physiology
Cerebellum  physiologyCerebellum  physiology
Cerebellum physiology
bigboss716
 

More from bigboss716 (20)

Autonomic nervous system pharmacology
Autonomic nervous system pharmacologyAutonomic nervous system pharmacology
Autonomic nervous system pharmacology
 
Pronator muscles anatomy and strengthening
Pronator muscles anatomy and strengtheningPronator muscles anatomy and strengthening
Pronator muscles anatomy and strengthening
 
suspension therapy and usage
   suspension therapy and usage   suspension therapy and usage
suspension therapy and usage
 
kinesiology basics
kinesiology basicskinesiology basics
kinesiology basics
 
Embryology limb defects
Embryology  limb defectsEmbryology  limb defects
Embryology limb defects
 
Twins (embryology)
Twins (embryology)Twins (embryology)
Twins (embryology)
 
lower limb anatomy MCQs
 lower limb anatomy MCQs lower limb anatomy MCQs
lower limb anatomy MCQs
 
Vision disorder
Vision disorderVision disorder
Vision disorder
 
Tens transcutaneous electrical nerve stimulator
Tens  transcutaneous electrical nerve stimulatorTens  transcutaneous electrical nerve stimulator
Tens transcutaneous electrical nerve stimulator
 
Pharmaco dyanamics studies
Pharmaco dyanamics studies Pharmaco dyanamics studies
Pharmaco dyanamics studies
 
Renin angiotensin system
Renin angiotensin systemRenin angiotensin system
Renin angiotensin system
 
Directly acting vasodilators
Directly acting vasodilatorsDirectly acting vasodilators
Directly acting vasodilators
 
Antihypertensives
Antihypertensives Antihypertensives
Antihypertensives
 
Bone pathology
Bone pathologyBone pathology
Bone pathology
 
The limbic system and the hypothalamus
The limbic system and the hypothalamusThe limbic system and the hypothalamus
The limbic system and the hypothalamus
 
Vestibular apparatus
Vestibular apparatusVestibular apparatus
Vestibular apparatus
 
Hypothalmus& thalmus
Hypothalmus& thalmusHypothalmus& thalmus
Hypothalmus& thalmus
 
Cerebral cortex
Cerebral cortexCerebral cortex
Cerebral cortex
 
Cerebral blood flow
Cerebral blood flowCerebral blood flow
Cerebral blood flow
 
Cerebellum physiology
Cerebellum  physiologyCerebellum  physiology
Cerebellum physiology
 

Recently uploaded

The Importance of Community Nursing Care.pdf
The Importance of Community Nursing Care.pdfThe Importance of Community Nursing Care.pdf
The Importance of Community Nursing Care.pdf
AD Healthcare
 
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...
Kumar Satyam
 
BOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptx
BOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptxBOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptx
BOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptx
AnushriSrivastav
 
Roti bank chennai PPT [Autosaved].pptx1
Roti bank  chennai PPT [Autosaved].pptx1Roti bank  chennai PPT [Autosaved].pptx1
Roti bank chennai PPT [Autosaved].pptx1
roti bank
 
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...
The Lifesciences Magazine
 
Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.
Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.
Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.
preciousstephanie75
 
一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证
一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证
一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证
o6ov5dqmf
 
POLYCYSTIC OVARIAN SYNDROME (PCOS)......
POLYCYSTIC OVARIAN SYNDROME (PCOS)......POLYCYSTIC OVARIAN SYNDROME (PCOS)......
POLYCYSTIC OVARIAN SYNDROME (PCOS)......
Ameena Kadar
 
Telehealth Psychology Building Trust with Clients.pptx
Telehealth Psychology Building Trust with Clients.pptxTelehealth Psychology Building Trust with Clients.pptx
Telehealth Psychology Building Trust with Clients.pptx
The Harvest Clinic
 
ICH Guidelines for Pharmacovigilance.pdf
ICH Guidelines for Pharmacovigilance.pdfICH Guidelines for Pharmacovigilance.pdf
ICH Guidelines for Pharmacovigilance.pdf
NEHA GUPTA
 
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...
ILC- UK
 
Antibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptxAntibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptx
AnushriSrivastav
 
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...Navigating Challenges: Mental Health, Legislation, and the Prison System in B...
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...
Guillermo Rivera
 
CANCER CANCER CANCER CANCER CANCER CANCER
CANCER  CANCER  CANCER  CANCER  CANCER CANCERCANCER  CANCER  CANCER  CANCER  CANCER CANCER
CANCER CANCER CANCER CANCER CANCER CANCER
KRISTELLEGAMBOA2
 
Jaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICE
Jaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICEJaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICE
Jaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICE
ranishasharma67
 
HEAT WAVE presented by priya bhojwani..pptx
HEAT WAVE presented by priya bhojwani..pptxHEAT WAVE presented by priya bhojwani..pptx
HEAT WAVE presented by priya bhojwani..pptx
priyabhojwani1200
 
💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...
💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...
💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...
ranishasharma67
 
Myopia Management & Control Strategies.pptx
Myopia Management & Control Strategies.pptxMyopia Management & Control Strategies.pptx
Myopia Management & Control Strategies.pptx
RitonDeb1
 
ABDOMINAL COMPARTMENT SYSNDROME
ABDOMINAL COMPARTMENT SYSNDROMEABDOMINAL COMPARTMENT SYSNDROME
ABDOMINAL COMPARTMENT SYSNDROME
Rommel Luis III Israel
 
Navigating Women's Health: Understanding Prenatal Care and Beyond
Navigating Women's Health: Understanding Prenatal Care and BeyondNavigating Women's Health: Understanding Prenatal Care and Beyond
Navigating Women's Health: Understanding Prenatal Care and Beyond
Aboud Health Group
 

Recently uploaded (20)

The Importance of Community Nursing Care.pdf
The Importance of Community Nursing Care.pdfThe Importance of Community Nursing Care.pdf
The Importance of Community Nursing Care.pdf
 
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...
 
BOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptx
BOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptxBOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptx
BOWEL ELIMINATION BY ANUSHRI SRIVASTAVA.pptx
 
Roti bank chennai PPT [Autosaved].pptx1
Roti bank  chennai PPT [Autosaved].pptx1Roti bank  chennai PPT [Autosaved].pptx1
Roti bank chennai PPT [Autosaved].pptx1
 
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...
Deep Leg Vein Thrombosis (DVT): Meaning, Causes, Symptoms, Treatment, and Mor...
 
Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.
Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.
Surgery-Mini-OSCE-All-Past-Years-Questions-Modified.
 
一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证
一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证
一比一原版纽约大学毕业证(NYU毕业证)成绩单留信认证
 
POLYCYSTIC OVARIAN SYNDROME (PCOS)......
POLYCYSTIC OVARIAN SYNDROME (PCOS)......POLYCYSTIC OVARIAN SYNDROME (PCOS)......
POLYCYSTIC OVARIAN SYNDROME (PCOS)......
 
Telehealth Psychology Building Trust with Clients.pptx
Telehealth Psychology Building Trust with Clients.pptxTelehealth Psychology Building Trust with Clients.pptx
Telehealth Psychology Building Trust with Clients.pptx
 
ICH Guidelines for Pharmacovigilance.pdf
ICH Guidelines for Pharmacovigilance.pdfICH Guidelines for Pharmacovigilance.pdf
ICH Guidelines for Pharmacovigilance.pdf
 
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...
 
Antibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptxAntibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptx
 
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...Navigating Challenges: Mental Health, Legislation, and the Prison System in B...
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...
 
CANCER CANCER CANCER CANCER CANCER CANCER
CANCER  CANCER  CANCER  CANCER  CANCER CANCERCANCER  CANCER  CANCER  CANCER  CANCER CANCER
CANCER CANCER CANCER CANCER CANCER CANCER
 
Jaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICE
Jaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICEJaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICE
Jaipur ❤cALL gIRLS 89O1183002 ❤ℂall Girls IN JaiPuR ESCORT SERVICE
 
HEAT WAVE presented by priya bhojwani..pptx
HEAT WAVE presented by priya bhojwani..pptxHEAT WAVE presented by priya bhojwani..pptx
HEAT WAVE presented by priya bhojwani..pptx
 
💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...
💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...
💘Ludhiana ℂall Girls 📞]][89011★83002][[ 📱 ❤ESCORTS service in Ludhiana💃💦Ludhi...
 
Myopia Management & Control Strategies.pptx
Myopia Management & Control Strategies.pptxMyopia Management & Control Strategies.pptx
Myopia Management & Control Strategies.pptx
 
ABDOMINAL COMPARTMENT SYSNDROME
ABDOMINAL COMPARTMENT SYSNDROMEABDOMINAL COMPARTMENT SYSNDROME
ABDOMINAL COMPARTMENT SYSNDROME
 
Navigating Women's Health: Understanding Prenatal Care and Beyond
Navigating Women's Health: Understanding Prenatal Care and BeyondNavigating Women's Health: Understanding Prenatal Care and Beyond
Navigating Women's Health: Understanding Prenatal Care and Beyond
 

Receptors

  • 2. • Student should be able to • understand the types of sensory receptors • enumerate and understand the properties of receptors
  • 3. SENSORY RECEPTORS • Information about the internal and external environment activates the CNS via a variety of sensory receptors. • These receptors are transducers that convert various forms of energy in the environment into action potentials in neurons. • Stimulus is an event or particular form of energy that evokes a specific functional reaction in an organ or receptor. (mechanical, chemical, EMG, temp)
  • 4. SENSE ORGANS • Receptors are dendritic endings of afferent neurons that are associated with non-neuronal cells forming sense organs.
  • 5. • The term Sensory unit means sensory axon and all its peripheral branches. • The receptive field of a sensory neuron is the particular part of the body surface in which a stimulus will trigger the firing of that neuron.
  • 6. CLASSIFICATION OF SENSORY RECEPTORSTYPE OF SENSATION • Mechanoreceptors • Thermoreceptors • Nociceptors • Electromagnetic • Chemoreceptors DISTANCE OF PERCEPTION • Teleceptors • Exteroceptors • Interoceptors • Proprioceptors
  • 7. CLASSIFICATION OF RECEPTORS • Mechanoreceptors Epidermis & dermis Joints, tendons, ligaments & muscles Cochlea Vestibular apparatus Baroreceptors in vessels • Thermoreceptors Warmth & cold • Nociceptors Pain • Electromagnetic Rods & cones • Chemoreceptors Taste & smell Carotid &aortic bodies Hypothalamus Osmo receptors
  • 8. TACTILE MECHANORECEPTORSENCAPSULATED • Meissner’s corpuscles in dermal papilla • Pacinian corpuscles in dermis, ligaments, joint capaules • Ruffni’s end organs in dermis and in deeper tissues NON-ENCAPSULATED • Free nerve endings in dermis, ligaments, cornea, bones • Hair end organs in hairy skin • Merkel’s discs in non hairy and hairy skin
  • 10.
  • 11. SENSORY CODING Receptors encode four elements of stimuli • Modality • Location • Intensity • Duration
  • 12. MODALITY OF SENSATION • Differential Sensitivity of Receptors for particular stimulus or specific energy for which it is designed • When nerve fiber from the receptors is stimulated the perception is that for which the receptor is specialized, no matter where and how that nerve is stimulated. This is Muller’s law of specific energy. • The specificity of nerve fibers for transmitting only one modality of sensation is called the labeled line principle.
  • 13. EXPLANNATION • Each nerve tract terminates at a specific point in the central nervous system, and the type of sensation felt when a nerve fiber is stimulated is determined by the point in the nervous system to which the fiber leads. • For instance if a pain fiber is stimulated, the person perceives pain regardless of what type of stimulus excites the fiber. • Likewise, if a touch fiber is stimulated by electrical excitation of a touch receptor or in any other way, the person perceives touch.
  • 14. LAW OF PROJECTION • No matter which part of a pathway you stimulate between the receptor and the brain center, your brain will locate the stimulus where receptors are (e.g. phantom limb) • reorganization of brain map in somatosensory cortex • Some believe it can be blocked by local anesthetics in spinal cord.
  • 15. • A phantom limb is the sensation that an amputated or missing limb is still attached to the body. • Approximately 60 to 80% of individuals with an amputation experience phantom sensations in their amputated limb, and the majority of the sensations are painful. • Phantom sensations may also occur after the removal of body parts e.g. after amputation of the breast, extraction of a tooth (phantom tooth pain) or removal of an eye (phantom eye syndrome)
  • 16. DALE’S LAW • At one type of synapse only one type of neurotransmitter is released
  • 17.
  • 18. TRANSDUCTION OF SENSORY STIMULI INTO RECEPTOR POTENTIAL AND NERVE IMPULSESReceptor Potentials When pressure is applied to pacinian corpuscle , a small non- propogated depolarizing potential develops called receptor potential.
  • 19. PROPERTIES OF RECEPTOR POTENTIAL • It is graded potential • It is non- propagated • It doesn't obey all or none law
  • 20. MECHANISMS OF RECEPTOR POTENTIALS. • Different receptors can be excited in one of several ways to cause receptor potentials: • (1) by mechanical deformation of the receptor, which stretches the receptor membrane and opens ion channels; • (2) by application of a chemical to the membrane, which also opens ion channels; • (3) by change of the temperature of the membrane, which alters the permeability of the membrane; or • (4) by the effects of electromagnetic radiation,
  • 21.
  • 22. RELATION OF THE RECEPTOR POTENTIAL TO ACTION POTENTIALS • When the receptor potential rises above the threshold for eliciting action potentials in the nerve fiber attached to the receptor, then action potentials occur. • More the receptor potential rises above the threshold level, the greater becomes the action potential frequency.
  • 23. RELATION OF THE RECEPTOR POTENTIAL TO ACTION POTENTIALS • More the receptor potential rises above the threshold level, the greater becomes the action potential frequency.
  • 24. RELATION BETWEEN STIMULUS INTENSITY AND THE RECEPTOR POTENTIAL. • Amplitude increases rapidly and then less rapid rise at high stimulus strength • the frequency of repetitive action potentials transmitted from sensory receptors also increase • But very strong stimulation decrease action potentials as well
  • 25. ADAPTATION OF RECEPTORS • Another characteristic of all sensory receptors is that they adapt either partially or completely to any constant stimulus after a period of time. • That is, when a continuous sensory stimulus is applied, the receptor responds at a high impulse rate at first and then at a progressively slower rate until finally the rate of action potentials decreases to very few or often to none at all.
  • 26. MECHANISMS BY WHICH RECEPTORS ADAPT • part of the adaptation results from readjustments in the structure of the receptor itself, • and part from an electrical type of accommodation in the terminal nerve fibril
  • 27. SLOWLY AND RAPIDLY ADAPTING RECEPTORS • Slowly Adapting Receptors Detect Continuous Stimulus Strength—The “Tonic” Receptors. • impulses from the muscle spindles and Golgi tendon apparatuses allow the nervous system to know the status of muscle contraction • Receptors of the macula in the vestibular apparatuses • pain receptors • baroreceptors of the arterial tree • chemoreceptors of the carotid and aortic bodies. • Rapidly Adapting Receptors Detect Change in Stimulus Strength—The “Rate Receptors,” “Movement Receptors,” or “Phasic Receptors.” • Pacinian and meissner’s • Importance of the Rate Receptors— Their Predictive Function.
  • 28. TYPES OF NERVE FIBERS
  • 29. • To classify nerve fibers • To understand the properties and differences of nerve fibers
  • 30. NERVE FIBERS THAT TRANSMIT DIFFERENT TYPES OF SIGNALS, AND THEIR PHYSIOLOGIC CLASSIFICATION nerve fibers come in all sizes between 0.5 and 20 micrometers in diameter— the larger the diameter, the greater the conducting velocity The range of conducting velocities is between 0.5 and 120 m/sec
  • 31. GENERAL CLASSIFICATION OF NERVE FIBERS In the general classification, the fibers are divided into types • A, B and C, • A&B are myelinated. C fibers are not • the type A fibers are further subdivided into • A α (annulospiral endings) • A β (touch and pressure) • A ɣ (motor to muscle spindles) • Aδ (Pain and temp) • B fibers are pre-ganglionic fibers • C fibers are post ganglionic and also transmit slow pain
  • 32. ALTERNATIVE CLASSIFICATION USED BY SENSORY PHYSIOLOGISTS • Group Ia Muscle spindle • Group Ib Golgi tendon organs • Group II Cutaneous tactile receptors • Group III Fibers carrying temperature, crude touch, and pricking pain sensations • Group IV Un-myelinated fibers carrying pain, itch, temperature, and crude touch sensations
  • 33. Diameter in micrometers Conduction velocity in m/sec Motor Fiber Type Aα 0.12-20 0.72-120 Extrafusal skeletal muscle fibers Aγ 0.12-8.2 0.12-48 Intrafusal muscle fibers B 0.21-33 0.86-18 Preganglionic autonomic fibers C 0.2-2 0.5-2 Postganglionic autonomic fibers
  • 34. Peripheral nerve fibers Afferents Diameter of nerve fibers in mm Conduction velocity in m/sec Receptors Sensory Fiber Type Aα Ia and Ib 0.13-20 0.80-120 m/sec Primary muscle spindles, Golgi tendon organ Aβ II 0.16-12 0.35-75 Secondary muscle spindles, skin mechanoreceptors Aδ III 0.11-5 0.15-30 Skin mechanoreceptors, thermal receptors, fast pain C IV 0.2-1.5 0.5-2 Slow pain and temp
  • 36. Two types of divergence • Amplifying type in same direction • Divergence into multiple tracts to enter multiple areas of brain
  • 38. CONVERGENCE OF SIGNALS • Convergence means signals from multiple inputs uniting to excite a single neuron. • Convergence from a single source. That is, multiple terminals from a single incoming fiber tract terminate on the same neuron. • Convergence can also result from input signals (excitatory or inhibitory) from multiple sources
  • 39. SOMATIC SENSATIONS AND MECHANICAL RECEPTORS DR. SADIA NAZIR ASSISTANT PROFESSOR PHYSIOLOGY LMDC
  • 40. • Classify somatic sensations • Classify mechanical receptors
  • 41. Classification of Sensations • The somatic senses are the nervous mechanisms that collect sensory information from all over the body. • Special senses, which mean specifically vision, hearing, smell, taste and equilibrium.
  • 42. CLASSIFICATION OF SOMATIC SENSES • The mechanoreceptive somatic senses, which include both tactile and position sensations. • The thermoreceptive senses, which detect heat and cold • The pain sense, which is activated by any factor that damages the tissues.
  • 43. MECHANORECEPTIVE SOMATIC SENSES • The tactile senses include touch, pressure, vibration, and tickle • the position senses include static position and rate of movement
  • 44. DETECTION AND TRANSMISSION OF TACTILE SENSATIONS • Touch, pressure, and vibration are all detected by the same types of receptors called tactile receptors. • There are at least six entirely different types of tactile receptors
  • 45. FREE NERVE ENDINGS • Free nerve endings, which are found everywhere in the skin and in many other tissues, can • detect touch and pressure
  • 46. MEISSNER’S CORPUSCLE • Elongated encapsulated nerve ending of a large (type AB) myelinated nerve fiber. • Inside the capsulation are many branching terminal nerve filaments. • These corpuscles are present in the non hairy parts of the skin . • Meissner’s corpuscles adapt in a fraction of a second after they are stimulated, • Detect low frequency vibration.
  • 47. MERKEL’S DISCS • The hairy parts and non hairy part of the skin also contain moderate numbers of expanded tip receptors • they transmit an initially strong but partially adapting signal and then a continuing weaker signal • adapts only slowly. • Therefore, they are responsible for giving steady-state signals
  • 48. IGGO DOME RECEPTOR • Merkel’s discs are often grouped together in a receptor organ called the Iggo dome receptor, which projects upward against the underside of the epithelium of the skin
  • 49. HAIR END-ORGAN • This receptor adapts readily and, like Meissner’s corpuscles, detects mainly • (a) movement of objects on the surface of the body or • (b) initial contact with the body.
  • 50. RUFFINI’S END-ORGANS • Multibranched, encapsulated endings, • These endings adapt very slowly • They are also found in joint capsules and help to signal the degree of joint rotation • Found in skin and deeper tissues
  • 51. PACINIAN CORPUSCLES • Lie both immediately beneath the skin and deep in the fascial tissues of the body. • They are stimulated only by rapid local compression of the tissues because they adapt in a few hundredths of a second. • Important for detecting tissue vibration or other rapid changes in the mechanical state of the tissues.
  • 52. • Position sense 1. Static 2. Rate of movement called kinesthesia • Receptors 1. Muscle spindles 2. Golgi tendon organs 3. Ruffni’s endings 4. Pacinian
  • 53. • Texture meissner & merkel • Localization meissner & merkel • Discrimination meissner • Vibration meissner & pacinian • Prolonged touch merkel’s • Prolonged deep touch & pressure ruffni’s
  • 54. TRANSMISSION OF TACTILE SIGNALS IN PERIPHERAL NERVE FIBERS • Transmit their signals in type A-beta nerve fibers that have transmission velocities ranging from 30 to 70 m/sec. • free nerve ending tactile receptors transmit signals mainly by way of the small type A-delta myelinated fibers that conduct at velocities of only 5 to 30 m/sec. • Some tactile free nerve endings transmit by way of type C unmyelinated fibers (up to 2 m/sec;) these send signals into the spinal cord and lower brain stem, mainly the sensation of tickle.
  • 55. DETECTION OF VIBRATION • Pacinian corpuscles can detect signal vibrations from 30 to 800 cycles per second and they also transmit their signals over type A-beta nerve fibers. • Meissner’s corpuscles detect vibrations from 2 to 80 cycles per seconds
  • 56. TICKLE AND ITCH • rapidly adapting mechanoreceptive free nerve endings elicit only the tickle and itch sensations. • These sensations are transmitted by very small type C, unmyelinated fibers similar to those that transmit the aching, slow type of pain.
  • 57. • Receptors afferents dorsal root ganglia gray column ascending tracts thalamus sensory cortex
  • 58.
  • 59.
  • 60.
  • 61. SENSORY PATHWAYS • Dorsal Column-medial lemsiscus pathway • Sensations carried: • Light touch • pressure • Tactile localisation • 2 point discrimination • Flutter and vibration • Stereognosis • Propioception • Graphesthesia • Large myleinated nerve fibres (fast) • Spatial orientation
  • 62. •DORSAL COLUMN MEDIAL LEMNISCUS PATHWAY •Nerve fibres enters through dorsal roots divides into medial +lateral barnches •Medial ascends in dorsal columns •Lateral further branches and synapse with local neurons •Some fibres are given off to the dorsal column •Some form local reflexes •Others form
  • 63. •Ascending fibres terminate on cuneate and gracile nuclei •Decussate to the opposite side immediately medial lemniscus •Fibers terminate in the thalamic sensory relay area, called the ventrobasal complex. •third-order nerve fibers project, mainly to • the postcentral gyrus of the cerebral cortex, (called somatic sensory area I) •also project to a smaller area in the lateral parietal cortex called somatic sensory area II).
  • 64.
  • 65. • the fibers from the lower parts of the body lie toward the center of the cord, whereas new fibres enter laterally. • In the thalamus, the tail end of the body represented by the most lateral portions of the ventrobasal complex and the head and face represented by medial areas of the complex. • because of the crossing of the medial lemnisci in the medulla, the left side of the body is represented in the right side of the thalamus, and the right side of the body in the left side of the thalamus. Spatial Orientation
  • 66.
  • 67. ANTEROLATERAL SYSTEM Transmits sensory signals that DO NOT require highly discrete localization • Composed of smaller, myelinated nerve fibers (transmission speeds 40 m/sec) • Less spatial orientation • Sensory modalities – wide range • Comprise of: • Anterior spinothalamic tract • Lateral spinothalamic tract
  • 68. ANTEROLATERAL SYSTEM • Pain • Thermal sensations (including warmth & cold) • Crude touch and pressure sensations • Tickle and itch sensations • Sexual sensations
  • 69. •From receptors (free nerve ending enter dorsal horn (cell bodies of these first order neurons are in the dorsal root ganglion) •Synapse with 2nd order within 1-2 segments •Second order neurons dorsal horn (at all levels). Their axons decussate in the anterior white and gray commisure •Joined by trigeminothalmic fibers in medulla, send collaterals to reticular formation (alertness to pain)
  • 70. •3rd order neurons VPL nucleus of thalamus. Their fibres ascend through the posterior limb of internal capsule corona radiate •4th order neurons of the cerebral cortex (Broadmans areas 3,1.2 Somatosensory cortex) •Some fibers from the second order neuron decussate and ascend as anterior spinothalmic tract •Both anterior & lateral spinothalamic tracts unite in MO forming spinal lemniscus
  • 71. ANTERIOR AND LATERAL SPINOTHALMIC TRACTS Some fibers carrying crude touch, tickle may ascend 8-10 spinal cord segments before synapsing with secondary neurons. Ascend more anteriorly as the anterior spinothalmic tract Secondary fibers decussate in anterior gray or white commissures. Acend to the medulla together spinal lemniscus
  • 72. • Dorsal Column–Medial Lemniscal System • 1. Touch sensations requiring a high degree of localization of the stimulus • 2. Touch sensations requiring transmission of fine gradations of intensity • 3. Phasic sensations, such as vibratory sensations • 4. Sensations that signal movement against the skin • 5. Position sensations from the joints • 6. Pressure sensations having to do with fine degrees of judgment of pressure intensity • Anterolateral System • 1. Pain • 2. Thermal sensations, including both warmth and cold sensations • 3. Crude touch and pressure sensations capable only of crude localizing ability on the surface of the body • 4. Tickle and itch sensations • 5. Sexual sensations
  • 73.
  • 74.
  • 75. Cortex: Broadmann’s areas (50) Central fissure: anterior to it motor cortex Posterior sensory cortex Occipital lobe visual Tempral Lobe Auditory SS1 and SS2 Located  aneterior part of parietal lobe SS1-high degree of localization
  • 76. Molecular layer External granular layer External pyramidal layer Internal granular layer Internal pyramidal layer Polymorphic layer
  • 77.
  • 78.
  • 79. FUNCTIONS OF SOMATOSENSORY AREA I • Localize and discriminate discretely the different sensations in the different parts of the body • judge critical degrees of pressure against the body • judge the texture, BILATERAL EXCISION OF SOMATOSENSORY AREA Pt is unable to • Localize and discriminate discretely the different sensations in the different parts of the body • judge critical degrees of pressure against the body • judge the texture, weights, shapes or forms of objects. This is called astereognosis. • Judge the shape by drawing. Agraphaesthesia
  • 80. Effect of Removing the Somatosensory Association Area—(5,7) Amorphosynthesis • The person loses ability to recognize complex objects and complex forms felt on the opposite side of the body. • He or she loses most of the sense of form of his or her own body parts on the opposite side and forgets that it is there . • When feeling objects, the person tends to recognize only one side of the object and forgets that the other side even exists.
  • 81. LESIONS OF DORSAL COLUMN TRACT • Sensory ataxia • Loss of vibration • Loss of tactile discrimination • Loss of tactile localization
  • 82. • Dorsal Column–Medial Lemniscal System • Touch sensations requiring a high degree of localization of the stimulus • Touch sensations requiring transmission of fine gradations of intensity • Phasic sensations, such as vibratory sensations • Sensations that signal movement against the skin • Position sensations from the joints • Pressure sensations having to do with fine degrees of judgment of pressure intensity • Anterolateral System • Pain • Thermal sensations, including both warmth and cold sensations • Crude touch and pressure sensations capable only of crude localizing ability on the surface of the body • Tickle and itch sensations • Sexual sensations
  • 83.
  • 84. • Dermatome Segment of skin supplied by the spinal nerve
  • 85.
  • 86. PAIN AND ANALGESIA SYSTEM DR. SADIA NAZIR ASSISTANT PROFESSOR PHYSIOLOGY LMDC
  • 87. PAIN IS A PROTECTIVE MECHANISM • Pain occurs whenever any tissues are being damaged, and it causes the individual to react to remove the pain stimulus.
  • 88. TYPES OF PAIN • Fast Pain • Slow Pain • Fast pain is felt within about 0.1 second after a pain stimulus is applied • Slow pain begins after 1 second or more and then increases slowly over many seconds and sometimes even minutes.
  • 89. QUALITIES OF PAIN • Fast pain is also described by many alternative names, such as sharp pain, pricking pain, acute pain, and electric pain • Slow pain also goes by many names, such as slow burning pain, aching pain, throbbing pain, nauseous pain, and chronic pain
  • 90. PAIN RECEPTORS • Are Free Nerve Endings • They are widespread in the superficial layers of the skin as well as in certain internal tissues, such as the periosteum, the arterial walls, the joint surfaces, and the falx and tentorium in the cranial vault. • Non-adapting Nature of Pain Receptors
  • 91. Three Types of Stimuli Excite Pain Receptors— • Mechanical • Thermal • Chemical
  • 92. • Some of the chemicals that excite the chemical type of pain are bradykinin, serotonin, histamine, potassium ions, acids, acetylcholine, and proteolytic enzymes • In addition, prostaglandins and substance P enhance the sensitivity of pain endings but do not directly excite them
  • 93. DUAL PATHWAYS FOR TRANSMISSION OF PAIN SIGNALS INTO THE CENTRAL NERVOUS SYSTEM • Peripheral Pain Fibers— • “Fast” (A delta) and “Slow” Fibers (C fibers) • The two pathways mainly correspond to the two types of pain— • a fast-sharp pain pathway and • a slow-chronic pain pathway.
  • 94. DUAL PATHWAYS FOR TRANSMISSION OF PAIN SIGNALS INTO THE CENTRAL NERVOUS SYSTEM FAST PAIN (NEOSPINOTHALAMIC PATHWAY) 1. Mechanical or thermal pain stimuli 2. A delta fibers at velocities between 6 and 30 m/sec. 3. They terminate mainly in lamina I (lamina marginalis) SLOW PAIN (PALEOSPINOTHALAMIC PATHWAY) 1. Mostly by chemical types of pain stimuli but sometimes by persisting mechanical or thermal stimuli. 2. C fibers at velocities between 0.5 and 2 m/sec. 3. laminae II and III of the dorsal horns, which together are called the substantia gelatinosa,
  • 95. Fast pain 4. most pass all the way to the thalamus (Ventrobasal) • Project to somatosensory cortex. 5. can be localized much more exactly in the different parts of the body than can slow-chronic pain. 6. Glutamate, the Probable Neurotransmitter of the Fast Pain Fibers SLOW PAIN 4.most terminate in one of three areas: (a) reticular nuclei (b) tectal area of the mesencephalon (c) periaqueductal gray region (d) Intralaminar nuclei and hypothalamus 5.Poorly localized. 6.Type C pain fiber terminals entering the spinal cord
  • 96. Pain Suppression (“Analgesia”) System in the Brain and Spinal Cord • Inhibition of pain signals at spinal cord by descending brain fibers • Encephalin secreting neurons in cord and brain stem • Inhibition of pain fibers by tactile incoming fibers
  • 97.
  • 98. Acupuncture analgesia (AA) • technique of relieving pain by inserting and manipulating threadlike needles at key points • acupuncture endorphin hypothesis • Acupuncture needles activate specific afferent nerve fibersCNSblocking pain transmission at both • the spinal-cord and brain levels through use of endorphins and closely related endogenous opiates.
  • 99.
  • 100.
  • 101. • The periaqueductal gray and periventricular areas of the mesencephalon and upper pons surround the aqueduct of Sylvius and portions of the third and fourth ventricles. Neurons from these areas send signals to • The raphe magnus nucleus, a thin midline nucleus located in the lower pons and upper medulla, and the nucleus reticularis paragigantocellularis, located laterally in the medulla. From these nuclei, second-order signals are transmitted down the dorsolateral columns in the spinal cord to • Pain inhibitory complex located in the dorsal horns of the spinal cord.
  • 102. INHIBITION OF PAIN TRANSMISSION BY SIMULTANEOUS TACTILE SENSORY SIGNALS • Stimulation of large type A beta sensory fibers from peripheral tactile receptors can depress transmission of pain signals from the same body area. • This presumably results from local lateral inhibition in the spinal cord. • It explains why such simple maneuvers as rubbing the skin near painful areas is often effective in relieving pain. • It also explains why liniments are often useful for pain relief.
  • 103. • Allodynia Non painful stimulus causes pain (Lesion of VPL of thalamus) • Hyperalgesia Hypersensitivity to pain A pain nervous pathway sometimes becomes excessively excitable;. • Possible causes of hyperalgesia are • Excessive sensitivity of the pain receptors themselves, which is called primary hyperalgesia (Burns)
  • 104. REFERRED PAIN • Often a person feels pain in a part of the body that is fairly remote from the tissue causing the pain. This is called referred pain. For instance, pain in one of the visceral organs often is referred to an area on the body surface.
  • 107. VISCERAL PAIN AND SURFACE PAIN VISCERAL PAIN • Highly localized types of damage to the viscera seldom cause severe pain. • True visceral pain is transmitted via pain sensory fibers within the autonomic nerve bundles, and the sensations are referred to surface areas of the body often far from the painful organ. SURFACE PAIN/PARIETAL PAIN • Parietal sensations are conducted directly into local spinal nerves from the parietal peritoneum, pleura, or pericardium, and these sensations are usually localized over painful area.
  • 108. VISCERAL” AND THE “PARIETAL” PAIN TRANSMISSION PATHWAYS
  • 109. CAUSES OF TRUE VISCERAL PAIN • Any stimulus that excites pain nerve endings in diffuse areas of the viscera can cause visceral pain. • Such stimuli include • ischemia of visceral tissue, • chemical damage to the surfaces of the viscera, • spasm of the smooth muscle of a hollow viscus, • excess distention of a hollow viscus, and stretching of the connective tissue surrounding or within the viscus. • Essentially all visceral pain that originates in the thoracic and abdominal cavities is transmitted through small type C pain fibers and, therefore, can transmit only the chronic-aching-suffering type of pain.
  • 110. Hyperalgesia • A pain nervous pathway sometimes becomes excessively excitable; this gives rise to hyperalgesia, which means hypersensitivity to pain. • Possible causes of hyperalgesia are • (1) excessive sensitivity of the pain receptors themselves, which is called primary hyperalgesia • (2) facilitation of sensory transmission, which is called secondary hyperalgesia.
  • 111. • Herpes Zoster (Shingles) • Herpesvirus infects a dorsal root ganglion. • This causes severe pain in the dermatomal segment served by the ganglion, thus eliciting a segmental type of pain that circles halfway around the body. • The disease is called herpes zoster, or “shingles,” because of a skin eruption that often ensues.
  • 112.
  • 113. • Tic Douloureux • Lancinating pain occasionally occurs in some people over one side of the face in the sensory distribution area (or part of the area) of the fifth or ninth nerves; This phenomenon is called tic douloureux (trigeminal neuralgia or glossopharyngeal neuralgia). • The pain feels like sudden electrical shocks, and it may appear for only a few seconds at a time or may be almost continuous.
  • 114.
  • 115.
  • 116. • Headache • Headaches are a type of pain referred to the surface of the head from deep head structures. • Pain-Sensitive Areas in Cranial Vault. • Tugging on the venous sinuses around the brain, • Damaging the tentorium, • Stretching the dura at the base of the brain can cause intense pain that is recognized as headache • Middle meningeal artery is a pain sensitive structure
  • 117.
  • 118. TYPES OF INTRACRANIAL HEADACHE • Brain tumors • Headache of Meningitis. • Headache Caused by Low Cerebrospinal Fluid Pressure. • Migraine Headache • Alcoholic Headache TYPES OF EXTRACRANIAL HEADACHE • Headache Resulting from Muscle Spasm. • Headache Caused by Irritation of Nasal and Accessory Nasal Structures. • Headache Caused by Eye Disorders
  • 119. THERMAL SENSATIONS • The human being can perceive different gradations of cold and heat, • from freezing cold • cold • cool • Indifferent • to warm • hot • burning hot.
  • 120. • Thermal gradations are discriminated by at least three types of sensory receptors: • cold receptors, • warmth receptors, • and pain receptors.
  • 121.
  • 122. BROWN-SÉQUARD SYNDROME • If the spinal cord is transected on only one side, the Brown-Séquard syndrome occurs. • All motor functions are blocked on the side of the transection in all segments below the level of the transection and at the level. • The sensations of pain, heat, and cold— sensations served by the spinothalamic pathway—are lost on the opposite side of the body in all dermatomes two to six segments below the level of the transection. • The dorsal and dorsolateral columns—kinesthetic and position sensations, vibration sensation, discrete localization, and two-point discrimination—are lost on the side of the transection in all dermatomes below the level of the transection.
  • 123. BROWN-SÉQUARD SYNDROME At the level Below the level Above the level LMN paralysis same side UMN paralysis same side Cutaneous anesthesia in the dermatomal segment of ipsilateral side Loss of pain and temp of contralateral side 2 to 5 segments below the level of lesion Altered sensations Loss of vibration, fine touch, tactile localization and discrimination in all