This document discusses the anatomy and physiology of the nervous system. It covers several topics:
1) The nervous system requires adequate space around neural tissue and attachments to surrounding structures. The space is less in males than females and developmental stenosis is more common in males.
2) The dura mater has various attachments inside and outside the cranium and spinal canal. Dural ligaments attach the dura to surrounding structures like bones.
3) The blood supply to the nervous system is critical. The spinal cord receives blood from various arteries but is most vulnerable between T4-T9 where the supply is least rich. Peripheral nerves also have extensive intrinsic blood flow.
4) Axonal transport systems move materials and
Thalamus-Anatomy,Physiology,Applied aspectsRanadhi Das
Thalamus is a very important relay station.
All general and special sensory impulses (except smell) & afferent impulses from RAS are integrated here.
Thalamus however is the center of pain and protopathic sensations.
It has other non sensory functions as well, like motor control, sleep, wakefulness.
It is the largest structure deriving from the embryonic diencephalon, the posterior part of the forebrain situated between the midbrain and the cerebrum.
The thalamus is part of a nuclear complex structured of 4 parts, the hypothalamus, epithalamus, prethalamus (formerly called ventral thalamus) and dorsal thalamus.
Neuroanatomy | 2. Cerebrum (1) Overview and Cerebral CortexAhmed Eljack
This is the second lecture in neuroanatomy presented and taught by Ahmed Eljack to second level medical students at Alneelain University.
This lecture discussed the divisions and landmarks of the cerebrum, important white matter bundles of the cerebrum and their functions, and the meninges.
Thalamus-Anatomy,Physiology,Applied aspectsRanadhi Das
Thalamus is a very important relay station.
All general and special sensory impulses (except smell) & afferent impulses from RAS are integrated here.
Thalamus however is the center of pain and protopathic sensations.
It has other non sensory functions as well, like motor control, sleep, wakefulness.
It is the largest structure deriving from the embryonic diencephalon, the posterior part of the forebrain situated between the midbrain and the cerebrum.
The thalamus is part of a nuclear complex structured of 4 parts, the hypothalamus, epithalamus, prethalamus (formerly called ventral thalamus) and dorsal thalamus.
Neuroanatomy | 2. Cerebrum (1) Overview and Cerebral CortexAhmed Eljack
This is the second lecture in neuroanatomy presented and taught by Ahmed Eljack to second level medical students at Alneelain University.
This lecture discussed the divisions and landmarks of the cerebrum, important white matter bundles of the cerebrum and their functions, and the meninges.
The origins of the endoneurial collagen of peripheral nerves and their roots have
not yet been determined. Ochoa (1976) has recently commented upon the presence
of collagen in endoneurial clefts some weeks before the earliest appearance of endoneurial
fibroblasts and consequently attributed collagen production to the immediately
adjacent Schwann cells. The occurrence of collagen in 'pockets' invaginated
into the Schwann cells of unmyelinated fibres (Gamble, 1964) was interpreted as
showing a tendency in such cells to enwrap any suitably sized and orientated structure,
but Thomas (1973) thought the phenomenon more probably indicative of a
capacity of Schwann cells to replace degenerated axons with newly formed collagen.
It was remarked also (Ochoa, 1971) that although collagen pockets may be quite
numerous in young adult human nerves they had not appeared in the sural nerve of
a human fetus of 18 weeks of intrauterine life, i.e. at a stage of development when Schwann cells are extremely active in the establishment of complex interrelationships with unmyelinated axons. In the course of work directed to the study of the development of the human trochlear nerve some observations have been made which are pertinent to the problem of the origin of the endoneurial collagen. They are reported and discussed below.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
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This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
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Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
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Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
2. NERVOUS SYSTEM RELATIONS SPACES AND
ATTACHMENTS
Adequate space is needed around the neural and
connective tissue and there must be enough space
at rest and during physiological movements of the
spine. The nervous system is attached to
surrounding tissues and structures.
Attachments need consideration in terms of those
attaching neural tissue into connective tissue, such
as the denticulate ligaments, and those attaching
connective tissue (and thus the neural tissue) onto
other structures, such as the dural ligaments.
3. NERVOUS SYSTEM RELATIONS SPACES AND
ATTACHMENTS
N.B Haset al (1983) have shown that the space
around neural tissue, both in the spinal canal and
the intervertebral foramen, is less in males than in
females.
These authors also point out that developmental
and degenerative stenosis is more common in the
male.
4. The external connections of the dura
Inside the cranium, the dura mater is loosely adhered
to the central portions of the cranial bones and tightly
adhered at the suture levels (Murzin & Gonunov 1979).
There is a firm attachment at the foramen magnum
and, at the caudal end, to the coccyx by the external
filum terminale. A network of dural ligaments
(Hoffman ligaments) attaches the anterior theca to the
anterior and and anterolateral aspect of the spinal canal
.
(Blikiia ,1969) noted that the dural ligaments around
L4 were stronger and more numerous than elsewhere
— so strong that they could not be displaced with a
probe.
5. The external connections of the dura
Thoracic dural ligaments tend to be filmier and
longer, In the cervical spine, they are shorter and
thicker (Romanes 1981).
The studies of Tencer et al (1985) have revealed
that, in the lumbar spine, dural ligaments, nerve
roots and trunks are of equal importance in the
distribution of forces.
6. Internal dural attachments
Inside the dural sac there are 21 pairs of denticulate
ligaments .These run from the pia mater to the dura
and are orientated to keep the cord central in the
dural theca. N.B Tani et al (1987) have shown that
the denticulate ligaments, as well as the filum
terminale, prevent excessive elongation of the cord
during flexion. Thickened denticulate ligaments
associated with cervical spondylosis have been
implicated in cord degeneration (Bedf ord et al
1952).
8. Attachments of the peripheral nervous system
The peripheral nerves are also attached to
surrounding tissue. However, they are allowed
movement in their nerve beds, less in some areas
than in others, such as where blood vessels enter or
where nerves branch.
9. Attachments of the peripheral nervous system
What is unmistakable is that, along the course of a
peripheral nerve, there are some areas where the
nerve is more attached than others, for example, the
common peroneal nerve at the head of the fibula,
and the radial nerve to the head of the radius.
Yet in other areas, a remarkble amount of
movement of over 1.5 cm occurs (McLelJan &
Swash 1976)
10. THE BASIS OF SYMPTOMS
Knowledge of three processes important to
understanding of symptom reproduction related to
the nervous System:
• The supply of blood to the nervous system .
• The axonal transport systems .
• The Innervation of the Connective tissues of the
nervous system .
All of these processes will be influenced by
mechanical deformation .
11. CIRCULATION
The nervous system consumes 20% of the available
oxygen in the circulating blood yet consists of 2% of
body mass (Dommjsse 1986). Among cells, neurones
are especially sensitive to alterations in blood flow.
Importance of blood supply :
An uninterrupted vascular supply is imperative for the
metabolic demands of normal neural function. Blood
supplies the necessary energy for impulse conduction
and also for the intracellular movement of the
Cytoplasm of the neurone.
12. CIRCULATION
There are extrinsic vessels supplying feeder arteries
to the nerve. Once inside the nervous system , there
is a ‘well dcveloped intrinsic system.
In many parts of the body, blood supply is so
assured that if some feeder vessels are
compromised the intrinsic system can provide
enough blood for normal neural function. With
such an assured supply, it may seem that the
nervous system Can be relatively independent of its
blood supply.
13. Vasculature of the spinal canal and neuraxis
These structures have a multiple supply :
1-The vertbral artery,
2- The deep cervical,
3- The posterior intercostal and the lumbar arteries supply
the vertbral column.
They also supply, via segmental subdivisions, the spinal
canal and contents.
At certain vertebral levels, medullary feeder branches
arise and join the longitudinally running anterior and
two small posterior spinal arteries.
14. Vasculature of the spinal canal and neuraxis
The anterior spinal artery supplies about 75% of the
cord. There are usually around eight medullary feeder
arteries (a branch of the cervical part of the vertebral
artry).
These arteries are more common in the lumbar and
cervical spines.
Most of the arteries enter the cord in the low cervical
spine and the lumbar spine.
During spinal movements these plexus areas have
limited movement in relation to the spinal canal (Louis
1981)
15. Vasculature of the spinal canal and neuraxis
When the cord is elongated the vessels running
longitudinally are stretched while those running
transversely are folded. The opposite effect occurs
on shortening of the cord (Fig. 1.)
16.
17. Vasculature of the spinal canal and neuraxis
The veins in the spinal canal are valveless and
under little pressure (Penn ing & Wilrnink 1981).
This allows flow reversibility and an
accommodating mechanism to sudden in-rushes of
blood, as may occur from coughing and straining.
18. Vasculature of the spinal canal
and neuraxis
Together with the CSF pressure, via the alterations
in the venous system, a balance of intraspinal canal
pressure is maintained.
N.B A critical vascular zone exists from the T4 to
T9 vertebral levels. The spinal canal is at its
narrowest and the blood supply is less rich in this
area (Dommisse 1974). This may be relevant in
syndromes such as the ‘T4 syndrome’ .
19. Vasculature of the peripheral nervous system
The extrinsic supply of the peripheral nerves is
such that it allows leeway for movement; that is,
there is slack in the feeder vessels so that a nerve
can glide without alteration in the blood supply.
In general, major feeder vessels enter nerves at
areas where there is minimal or no nerve movement
in relation to surrounding tissue.
20. Vasculature of the peripheral nervous system
Examples of this are at the elbow for the median
and radial nerves. However, if part of the extrinsic
supply is occluded, the intrinsic supply is also
sufficient for the needs of the nerve fibres
(Lundborg 1970, 1975).
21. Vasculature of the peripheral nervous system
The intrinsic vascular system is extensive, linking
endoneuriurn, perineurium and epineurium.
Under normal conditions, only part of the intranural
vascular system is used.
However, if traumatised, many more vessels come
into use (Lundborg 1970). Intraneural blood flow is
reversible and collateral systems exist.
22. Vasculature of the peripheral nervous system
Intranural blood vessels are sympathetically
innervated (Hromada 1963, Lundborg 1970,
Appenzeller ci al 1984).
According to Appenzejler et al (1984), the nerve
supply to particular blood vessel arises from the
nerve trunk that: the blood vessel supplies. This
probably allows an adjustable blood supply for
functional demands on the nerve.
23. Vasculature of the peripheral nervous system
N.B Stretch and compression will surely affect the
circulation, although, the mechanisms are not fully
understood.
Strech will lessen the diameter of the longitudinally
running vessels, plus raise intrafascicular pressure
and perhaps result in squeezing closed the vessels
crossing the perineurium.
24. Vasculature of the peripheral nervous system
N.B Arrest of blood flow will begin at
approximately 8% elongation (rabbit sciatic tract)
and complete arrest will occur at approximately
15% elongation (Lundborg & Rydevik 1973, Ogata
& Naito 1986).
25. The blood nerve-barriers
A slightly positive pressure exists in the
intrafascicular environment. This tissue pressure is
referred to as the endoneurial fluid pressure (EFP)
and is probably maintained by the elasticity of the
perineurium.
The barrier function is bi-directional. As well as
protection from the exterior, this mechanism means
that if the intrafascicular pressure increases, such as
from an oedematous reaction (Lundborg & Rydcvik
1973), the barrier may close.
26. The blood nerve-barriers
A good example of the protective function of the
diffusion barrier is where peripheral nerves travel
through infected areas without nerve conduction
being altered .The perineurial barrier is also
resistant to trauma.
27. AXONAL TRANSPORT SYSTEMS
Within the cytoplasm of all Cells there is
movcment of materials and substances.
The cytoplasm of the neurone (axoplasm) is no
different.
However , due to the length of the axon and its
function, speciaized intracellular movement
mechanisms occur.
28. AXONAL TRANSPORT SYSTEMS
The volume of material in an axon and teminals
may be thousands of times as great as in the cell
body (Lundborg 1988).
Mammalian axoplasm is quite viscous, about five
times that of water (Haak er al 1976).
Of necessity, the intracellular transport
mechanisms arc complex. These mechanisms are
referred to as axonal transport systems and are a
major direction for research in present day
neurological science.
29. AXONAL TRANSPORT SYSTEMS
The axon contains smooth endoplasimic reticulum,
ribosomes, microtubules and neurofilaments
comprised of actin like material — all structures
likely to be part of the axoplasmic transport
mechanisms.
N.B Human movement plays a role in this
intracellular motility.
30. AXONAL TRANSPORT SYSTEMS
Within the axon, the flow of substances is constant
and controlled.
From the cell body to the target tissues (antegrade
flow) there is a fast and a slow transport system.
From the target tissues to the cell body there is a
(retrograde flow) of axoplasm (Fig. 1.28).
This bi-directional flow is evident because a nerve
will swell both distally and proximally from
circumferential pressure (Mackinnon & Dellon
1988).
31. D deridrite, N nucleus, M mitochondria, SC synaptic cleft, TT targcc
tissue
Axoplasmic transport
32. AXONAL TRANSPORT SYSTEMS
Antegrade transport
Materials produced in the cell body are transported
along the axon at various velocities.
Two groups based on the speed of transport, can be
identified.
(A) The fast transport moves at approximately 400
mm per day and the substances carried such as
neurotransmitters and transmitter vesicles, are for
use in transmission of impulses at the synapse
(Droz et al 1975).
33. AXONAL TRANSPORT SYSTEMS
This transport depends on an uninterrupted supply
of energy from the blood. Various toxic substances
and deprivation of blood will slow or block the
transport (Ochs 1974).
34. AXONAL TRANSPORT SYSTEMS
(B) In the slow antegrade transport (1—6 mm per
day), cytoskeletal material such as microtubules
and neurofilaments are carried (Levine & Willard
1980 McL.ean et al 1983)
Essentially, the slow transport exists for
maintenance of the structure of the axon.
The exact mechanisms of transport are unknown.
35. AXONAL TRANSPORT SYSTEMS
Retrograde transport
Retrograde transport from target tissues to the cell
body moves rapidly (approx 200 mm per day).
The system carries recycled transmitter vesicles and
extracellular materials such as neurite growth
promoting factors from the nerve terminal or from
damaged segments of nerve.
36. AXONAL TRANSPORT SYSTEMS
N.B It also seems very likely that the retrograde
flow carries "trophic messages" about the status of
the axon, the synapse and the general environment
around the synapse, including the target tissues
(Kristensson & Olsson 1977, Varon & Adler 1980,
Bisby 1982).
37. AXONAL TRANSPORT SYSTEMS
If the retrograde flow is altered by physical
constriction or from loss of blood flow, nerve cell
body reactions are induced (Ochs 1984, Dahlin &
McLean 1986, Dahlin et al 1987).
Viruses, such as herpes simplex, can be transported
via the retrograde transport to the cell body
(Kristensson 1982).
38. AXONAL TRANSPORT SYSTEMS
An understanding of the concepts of axonal
transport is important for physiotherapists
employing mobilisation of the nervous system as a
treatment.
As Korr has suggested for some years (1978, 1985)
many of the disorders we treat and the responses
from treatment may be related to the axonal
transport systems.
39. AXONAL TRANSPORT SYSTEMS
Knowledge of these systems is also important in
order to understand the development of symptoms
along the nervous system (ie, double crush,
multiple crush synd romes) and the need to treat
often more than the local area for optimum results.
40. INNERVATION OF THE NERVOUS SYSTEM
The connective tissues of the nervous system are
innervated.
They are, thus, able to be a source of symptoms.
This innervation also means that the Connective
tissues of the nervous system can contribute o
altered sensory input in the same way that muscle,
joint and other tissue can.
41. The meninges
Dura mater is innervated by segmental, bilateral,
sinuvertebral nerves, first described by Luschka
(1850). (Meningeal Branch Of Spinal Nerves)
Each sinuvertebral nerve emerges distal to the
dorsal root ganglion, from the union of a somatic
root arising from the ventral rami and an autonomic
root from the grey rami communicate or a
sympathetic ganglion .
42.
43. The meninges
As well as supply to the dura, branches of the
Sinuvertebral nerve innervate
- The posterior longitudinal ligament,
-Periosteum,
-Blood vessels
And the annulus fibrosis (Edgar & Ghadially 1975,
Bogduk 1983).
44.
45. The meninges
N.B The innervation density varies depending on
the spinal segment.
It is richer in the superficial dural layers than in
those deeper.
Root sleeves at cervical and lumbar levels have a
richer nerve supply than the thoracic root sleeves
(Cuauco et al 1988).
46. The meninges
N.B All recent authors on the subject agree that the
ventral aspect of the dura mater has a far denser
innervation than the dorsal aspect .
Towards the midline, the dorsal dura may be
completely insensitive (Groen ct al 1988).
47. The connective tissues of nerve roots
The ventral nerve root connective tissues receive
their innervation from fibres Originating in the
dorsal root ganglion.
Connective tissues of the anterior nerve roots are
innervated by fine branches from the sinuvertebral
nerve (Hromada 1963).
48. The peripheral nervous system
The connective tissues of peripheral nerves, nerve
roots and the autonomic nervous system have an
intrinsic innervation: the ‘nervi nervorum’ from
local axonal branching.
Free nerve endings have been observed in the
perineurium, epineurium and endoneurium .
Thomas (1982) believes that the nervi nervorum
must be Considered a source of symptoms in
diabetic neuropathy and in inflammatory
polyneuropathics.
49. The innervation of the connective tissues of peripheral
nerve
The nervi
nervorurm
E epineurium,
BV blood
vessel,
NN nervi
nervorum,
NF nerve fiber
P perineurium,
PVP
perivascular
plexus
50. The peripheral nervous system
Sunderlarid (1978) considers the pain from local
pressure on a nerve to be due to the nervi
nervorum.
The innervation of the nervous system cannot be
neglected — it seems very likely that it plays a part
in adverse tension syndromes.
51. The peripheral nervous system
Perhaps innervation could be regarded as a
protective mechanism for the nervous system,
symptom production being a warning that the
impulse conducting mechanisms may be in danger
from mechanical or chemical compromise.