4. NERVOUS SYSTEM
ā¢ It is the chief controlling &
coordinating system of the body
ā¢ There are about 200 billion
neurons in an adult brain
ā¢ The sensory part collects
information from surroundings &
helps in gaining knowledge &
experience.
ā¢ The motor part is responsible for
responses of the body.
NERVOUS
SYSTEM
Central nervous
system
Brain Spinal cord
Peripheral nervous
system
1.Motor
division
ā¢Somatic
nervous
system
1.Autonomous
nervous
system
Sensory
division
Inderbir Singh's Textbook of Human Neuroanatomy
6. STRUCTURE OF NEURON
ā CELL BODY
ā Form grey matter & nuclei in CNS,
ganglia in PNS
ā CELL PROCESSES
ā Dendrites- multiple, short, richly
branched
ā Axons
Inderbir Singh's Textbook of Human Neuroanatomy
7. CLASSIFICATION OF NEURONS
A/c to number
of processes
UNIPOLAR
NEURONS
Mesencephalic nucleus
of fifth nerve
BIPOLAR NEURONS
First neuron of retina,
ganglia of eighth nerve
and olfactory mucosa
PSEUDOUNIPOLAR
NEURONS
Dorsal nerve root
ganglia and sensory
ganglia of cranial nerves
MULTIPOLAR
NEURONS
All motor and
internuncial neurons
Inderbir Singh's Textbook of Human Neuroanatomy
8. Inderbir Singh's Textbook of Human Neuroanatomy
FUNCTIONAL
CLASSIFICATION OF
NEURONS
Sensory
neurons
Primary
neurons
Secondary
neurons
Tertiary
neurons
Motor
neurons
Somatic
motor
neurons
Autonomic
neurons
18. BD Chaurasias human anatomy volume
ā ANOSMIA-loss of olfaction
ā with ageing
ā occurs in severe injuries which results in separation of olfactory bulb from the olfactory
nerves & the nerve gets torn.
ā Temporary in allergic rhinitis
ā Frontal lobe abscess presses on the olfactory bulb
ā UNCINATE FITS- Lesions of lateral olfactory area may cause temporal lobe epilepsy or
uncinate fits which are characterized by imaginary disagreeable odors with involvement
of tongue & lips.
22. Inderbir Singh's Textbook of Human Neuroanatomy
OPTIC PATHWAY
STRUCTURES IN VISUAL PATHWAY
ā¢ Retina
ā¢ Optic Nerve
ā¢ Optic Chiasma
ā¢ Optic Tract
ā¢ Lateral Geniculate Body
ā¢ Optic Radiation
ā¢ Visual Area In Cortex
23.
24. ā * SCOTOMA- Lesion in the retina forms blind spots
ā OPTIC NERVE DAMAGE- Complete blindness of eye
ā PAPILLOEDEMA- Results due to increased intracranial
pressure & leads to swelling of optic disc
ā OPTIC NEURITIS- Lesion of optic nerve resulting in
visual acuity
Inderbir Singh's Textbook of Human Neuroanatomy
30. Inderbir Singh's Textbook of Human Neuroanatomy
COURSE
INTRANEURAL COURSE
Fibres arise from nucleus &
pass ventrally
BASE OF BRAIN
Attached to oculomotor sulcus
CAVERNOUS SINUS
IN THE ORBIT
through middle part of superior
orbital fissure
UPPER DIVISION
supplies superior rectus & part
of levator palpebrae superioris.
LOWER DIVISION
Medial rectus, inferior rectus,
inferior oblique
33. Inderbir Singh's Textbook of Human Neuroanatomy
ā Paralysis of third nerve results in-
ā Ptosis (dropping of upper eyelid- LPS
affected)
ā lateral squint,
ā dilatation of pupil (fixed pupil )
ā loss of accommodation
ā , diplopia,
ā slight proptosis
ā Superior divisonal occulomotor
nerve palsy can also be caused by
fronto-ethmoidal sinusitis
ā COMPRESSION OF OCCULOMOTOR
NERVE- It can be due to extradural
haematoma which leads to dilatation
of pupil.
42. DIVISIONS OF TRIGEMINAL
NERVE
TRIGEMINAL
NERVE
Ophthalmic
nerve
Carries sensory fibres
from structures
derived from
frontonasal process
Maxillary nerve
Conveys afferent fibres
from structures derived
from maxillary process
Mandibular
nerve
Carries sensory
fibres derived from
mandibular process
Inderbir Singh's Textbook of Human Neuroanatomy
52. (Ref- Christian Nordqvist-Trigeminal neuralgia- Symptoms, causes &
treatment-Medical news today- 23 August 2017)
ļ TRIGEMINAL NEURALGIA
ā Trigeminal neuralgia (TN) is a relatively rare neuropathic disorder, characterized by extremely painful
episodic facial pain involving one or more trigeminal nerve branches.
ā Based on the International Classification of Headache Disorders- 3rd Edition (ICHD-3) TN is classified
into three: Classical TN, Secondary TN, and Idiopathic TN, based on the presence or absence of an
apparent disease process that could explain the neuralgia
ā Flaccid paralysis of muscles of mastication
ļ Hypoacusis- Partial deafness to low pitched sounds due to paralysis of tensor tympani muscle
ļ ATYPICAL TRIGEMINAL NEURALGIA- It is a variation of typical TN. Pain may be burning, aching,
cramping rather than sharp & stabbing. It occurs on one side of face & extends into upper neck or back
of scalp.
ā Quality of pain related to TN is described as electric shock-like, sharp, stabbing, or shooting, often
triggered by immaterial sensory input such as washing face, brushing, wind blow, and talking
54. BMC Oral Health , Clinical characterstics and associated factors of
55. Aurstralian Endodontic Journal , Trigeminal nerve injuries
infiltration dentistry provides significantly better for
pulpal anaesthesia in the anterior mandible compared
with inferior dental block (IDBs), is suitable for exodontia
in adults and children , is ideal for implant surgery is
suitable for periodontal surgery ,improved patient
comfort. Patients will undoubtedly prefer having full
lingual sensation and shorter duration LA anaesthesia
after dental treatment
59. Journal of Ophthalmic & Vision Research, 8(2), 160ā171. 3. Bagheri, A.,
Babsharif, B., Abrishami, M., Salour, H., & Aletaha,
ā Failure of abduction of the
affected eye
ā Commonest false localising
sign with raised intracranial
pressure
ā Diplopia due to paralysis of
right lateral rectus muscle
66. https://www.health.harvard.edu/pain/bells-palsy-overview
ā¢ BELLS PALSY- Sudden paralysis of facial nerve
at stylomastoid foramen causes inability to close
mouth, asymmetry at corner of mouth, loss of
wrinkling on forehead.
ā¢ Lesion at chorda tympani nerve- bells palsy+ loss
of taste sensation from ant two-third of tongue
ā¢ UPPER MOTOR NEURON PALSY- Paralysis of
contralateral lower quadrant of face
ā¢ LOWER MOTOR NEURON PALSY- Paralysis
of ipsilateral half of face
ā¢ CROCODILE TEARS SYNDROME-
Lacrimation occurs during eating due to abberant
regeneration after trauma
72. BD Chaurasias Human Anatomy Volume 3
ā VERTIGO- Illusion of rotatory movement due to disturbed orientation of body
ā TINNITIS- Sensation of buzzing, ringing, hissing or singing quality
ā MENIEREāS SYNDROME- Recurrent attacks of tinnitus, vertigo & hearing loss & sensitivity to
noises
ā ACOUSTIC NEUROMA- Benign tumor that affects nerves running from inner ear to brain Treatment
includes- Stereostatic radiosurgery & Microsurgical removal
ā DEAFNESS
ā CONDUCTIVE DEAFNESS- Failure of sound waves to reach to the cochlea
ā SENSORINEURAL DEAFNESS- Failure of production of action potential due to cochlear disease
ā CORTICAL DEAFNESS- Bilateral or dominant posterior temporal lobe lesion
77. BD chaurasias Human Anatomy volume 3
ļ§ GLOSSOPHARYNGEAL NEURALGIA- Short, sharp severe attacks of pain affecting posterior part of
pharynx
ļ§ Pharyngitis causes referred pain to ear
ļ§ Lesions cause
ā Absence of parotid secreations , post 1/3rd tongue taste loss
ā Loss of pain sensations from tongue , tonsils ,pharynx , soft palate
ā Absent gag reflex
82. BD Chaurasias Human Anatomy Volume 3
ā¢ Irritation of auricular branch of vagus in external ear
causes
ā¢ Persistent cough
ā¢ Vomiting
ā¢ Sudden cardiac inhibition
ā¢ Sensory ganglion may have viral infection of herpes
zoster & vesicles appear.
ā¢ Recurrent laryngeal nerve paralysis causes hoarseness
& dysphonia
ā¢ Tested clinically by comparing palatal arches on both
sides. On paralyzed side, no arching is present & uvula
is pulled to normal side.
ā¢ Nasal regurgitation of liquids
ā¢ Nasal twang & hoarseness of voice
ā¢ Flattening of palatal arch
ā¢ Vocal cords in cadaveric position
ā¢ Dysphagia
90. BD Chaurasias Human Anatomy Volume 3
Clinically tested by asking patient
to protrude his tongue. If the
nerve is paralyzed the tongue
deviates to paralyzed side
ā SUPRANUCLEAR LESION
ā Paralysis without wasting
ā Tongue moves sluggishly
ā Defective speech
ā Tongue deviates to opposite side on
protrusion
ā INFRANUCLEAR LESION
ā Paralysis of tongue on that side
ā Gradual atrophy of paralyzed half of tongue
ā Tongue looks shrunken
92. REFERNCES
ā¢ Inderbir Singh's Textbook of Human Neuroanatomy
ā¢ BD Chaurasia Human Anatomy volume 3
ā¢ Snellās Clinical Anatomy by Region
ā¢ Cunninghamās Manual of Practical Anatomy
ā¢ https://hms.harvard.edu/news/how-covid-19-causes-loss-smell
ā¢ Dovepress Journal of eye and brain
ā¢ Indian Jouranl of Opthamology
ā¢ Christian Nordqvist-Trigeminal neuralgia- Symptoms, causes & treatment-Medical news today- 23 August 2017
ā¢ Journal of Ophthalmic & Vision Research, 8(2), 160ā171. 3. Bagheri, A., Babsharif, B., Abrishami, M., Salour, H.,
& Aletaha,
ā¢ Aurstralian Endodontic Journal , Trigeminal nerve injuries
ā¢ BMC Oral Health , Clinical characterstics and associated factors of trigeminal neuralgia
ā¢ https://www.health.harvard.edu/pain/bells-palsy-overview
ā¢ https://www.physio-pedia.com/Adult-onset_Idiopathic_Torticollis
Editor's Notes
Autonomous nervous system
- involuntary
Sympathetic nervous
system
Parasympathetic nervous system
Enteric nervous system
Somatic nervous system
- voluntary
Sympathetic nervous system
Origin ā thoracolumbar outflow : T2 āL2-L3
Widely distributed
Adrenergic system
Parasympathetic nervous system
Origin ā craniosacral outflow : 3,7,9,10 , S2-S4
In head ,neck and trunk
Cholinergic system
It innervates viscera
ENTERIC NERVOUS SYSTEM
* GIT
*Pancreas
*Gall bladder
According to Area of Innervation ā¢ Somatic afferent fibres: Carry impulses from skin, bones, muscles, and joints to the CNS ā¢ Somatic efferent fibres: Carry impulses from CNS to the skeletal muscles ā¢ Visceral afferent fibres: Carry impulses from visceral organs and blood vessels to the CNS ā¢ Visceral efferent fibres: Carry impulses from CNS to the cardiac muscle, glands, and smooth muscles According to Diameter and Velocity of Conduction ā¢ A (subdivided into Ī±, b, g, Ī“) ā¢ B ā¢ C (unmyelinated) Sensory nerve fibres are also classified into I, II, III and IV Details of diameter and conduction velocity in the peripheral nerves with examples are given in Table 1.4. Presence of myelin sheath ā¢ Myelinated ā¢ Unmyelinated
1,2,8 : pure sensory 3,4,6,11,12 : pure motor Rest : mixed
Sensory nucleus of the trigeminal nerve
The sensory nucleus of the trigeminal nerve is a large cell group
that receives the primary afferents of the trigeminal nerve. It extends
caudally into the cervical spinal cord and rostrally into the midbrain;
its principal divisions are the spinal trigeminal, principal sensory and
mesencephalic nuclei (see Figs 21.10ā21.12) (Nieuwenhuys et al 2008;
Olszewski 1950).
On entering the pons, the fibres of the sensory root of the trigeminal
nerve run dorsomedially towards the principal sensory nucleus, which
is situated at this level. Before reaching the nucleus, approximately 50%
of the fibres divide into ascending and descending branches; the others
ascend or descend without division. The descending fibres, of which
90% are less than 4 Āµm in diameter, form the spinal tract of the trigeminal nerve, which embraces the spinal nucleus of the trigeminal nerve
and reaches the upper cervical spinal cord (see Figs 21.6ā21.8; Fig.
21.10). There is a precise somatotopic organization within the tract (see
Fig. 21.1). Fibres from the ophthalmic division of the trigeminal nerve
lie ventrally, those from the mandibular division lie dorsally, and those
from the maxillary division lie between. The tract is completed on its
dorsal rim by fibres from the sensory roots of the facial, glossopharyngeal and vagus nerves. All of these fibres synapse in the pars caudalis of
the spinal nucleus of the trigeminal nerve.
The detailed anatomy of the spinal tract of the trigeminal nerve
excited early clinical interest because it was recognized that dissociated
sensory loss could occur in the trigeminal area. For example, in Wallenbergās syndrome (lateral medullary syndrome), occlusion of the posterior inferior cerebellar artery (a branch of the vertebral artery) leads
to loss of pain and thermal sense on the ipsilateral half of the face with
retention of common sensation (Haines 2013). Neurosurgery in this
region, as early as the 1890s, attempted to alleviate paroxysmal trigeminal neuralgia. The introduction of medullary tractotomy confirmed that
dissociated thermoanalgesia of the face was associated with destruction
of the tract.
There are conflicting opinions on the pattern of termination of the
fibres in the spinal nucleus. It has long been held that fibres are organized rostrocaudally within the tract. According to this view, ophthalmic
fibres are ventral and descend to the lower limit of the first cervical
spinal segment, and maxillary fibres are central and do not extend below
the medulla oblongata, whilst mandibular fibres are dorsal and do not extend much below the mid-medullary level. The results of section of
the spinal tract in cases of severe trigeminal neuralgia support this
distribution. It was found that a section 4 mm below the obex rendered
the ophthalmic and maxillary areas analgesic, but tactile sensibility,
apart from the abolition of ātickleā, was much less affected. To include
the mandibular area it was necessary to section at the level of the obex.
More recently, it has been proposed that fibres are arranged dorsoventrally within the spinal tract. There appear to be sound anatomicophysiological and clinical reasons for believing that all divisions
terminate throughout the whole nucleus, although the ophthalmic division may not project fibres as far caudally as the maxillary and mandibular divisions. Fibres from the posterior face (adjacent to C2)
terminate in the lower (caudal) part, whilst those from the upper lip,
mouth and nasal tip terminate at a higher level. This can give rise to a
segmental (cross-divisional) sensory loss in syringobulbia. Tractotomy
of the spinal tract, if carried out at a lower level, can spare the perioral
region, a finding that would accord with the āonion-skinā pattern of loss
of pain sensation. However, in clinical practice, the progression of
anaesthesia on the face is commonly ādivisionalā rather than strictly
āonion-skinā in distribution.
Fibres of the glossopharyngeal, vagus and facial nerves subserving
common sensation (general somatic afferent) enter the dorsal region
of the spinal tract of the trigeminal nerve and synapse with cells in the
caudal part of the spinal nucleus. Consequently, operative section of
the dorsal part of the spinal tract results in analgesia that extends to the
mucosa of the tonsillar sinus, the posterior third of the tongue and
adjoining parts of the pharyngeal wall (supplied by the glossopharyngeal nerve), and the cutaneous areas of the ear. Other afferents that
reach the spinal nucleus are from the dorsal roots of the upper cervical
nerves and from the sensoryāmotor cortex.
The spinal nucleus of the trigeminal nerve consists of three parts:
the pars oralis (which adjoins the principal sensory nucleus); the pars
interpolaris; and the pars caudalis (which is continuous with the dorsal
horn of the spinal cord). The pars caudalis is different from the other
parts because it has a structure analogous to that of the dorsal horn of
the spinal cord, with a similar arrangement of cell laminae (subnuclei
zonalis, gelatinosus and magnocellularis), and is involved in trigeminal
pain perception. Cutaneous nociceptive afferents and small-diameter
muscle afferents terminate in layers I, II, V and VI of the pars caudalis
(see Fig. 21.1). Low-threshold mechanosensitive afferents of AĪ² neurones terminate in layers III and IV of the pars caudalis and in the rostral
(interpolaris, oralis, principal sensory) nuclei.
Many of the neurones in the pars caudalis that respond to cutaneous
or tooth-pulp stimulation are also excited by stimulation of jaw or
tongue muscles. This indicates that convergence of superficial and deep
afferent inputs via wide-dynamic-range or nociceptive-specific neurones
occurs in this nucleus. Similar convergence of superficial and deep
inputs occurs in the rostral nuclei and may account for the poor localization of trigeminal pain, and for the spread of pain, which often makes
diagnosis difficult.
There are distinct subtypes of cells in lamina II. Afferents from
āhigher centresā arborize within it, as do axons from nociceptive and
low-threshold afferents. Descending influences from these higher
centres include fibres from the periaqueductal grey matter and from the
nucleus raphe magnus and associated reticular formation.
The nucleus raphe magnus projects directly to the pars caudalis,
probably via enkephalin, noradrenaline (norepinephrine) and 5-HT
(5-hydroxytryptamine, serotonin)-containing terminals. These fibres
directly, or indirectly through local interneurones, influence pain perception. Stimulation of periaqueductal grey matter or nucleus raphe
magnus inhibits the jaw-opening reflex to nociception, and may induce
primary afferent depolarization in tooth-pulp afferents and other nociceptive facial afferents. Neurones in the pars caudalis can be suppressed
by stimuli applied outside their receptive field, particularly by noxious
stimuli. The pars caudalis is an important site for relay of nociceptive
input and functions as part of the pain āgate controlā. However, rostral
nuclei may also have a nociceptive role. Tooth-pulp afferents via widedynamic-range and nociceptive-specific neurones may terminate in
rostral nuclei, which all project to the subnucleus caudalis.
Most fibres arising in the trigeminal sensory nuclei cross the midline
and ascend as trigeminothalamic fibres (trigeminal lemniscus). They
end in the contralateral ventral posteromedial thalamic nucleus, from
which third-order neurones project to the cortical postcentral gyrus
(areas 3, 1, 2). However, some trigeminal nuclear efferents ascend to
the ipsilateral ventral posteromedial nucleus.
Fibres from the pars caudalis, especially from laminae I, V and VI,
also project to the rostral trigeminal nuclei, cerebellum, periaqueductal
grey of the midbrain, parabrachial area of the pons, the brainstem
reticular formation and the spinal cord. Fibres from lamina I project to
the subnucleus medius of the medial thalamus
Vagal nucleus
The vagal nucleus (the dorsal motor nucleus of the vagus) lies slightly
dorsolateral to the hypoglossal nucleus, from which it is separated by
the nucleus intercalatus. It extends caudally to the first cervical spinal
segment and rostrally to the open part of the medulla under the vagal
trigone in the floor of the fourth ventricle (see Fig. 21.8).
The vagal nucleus is a general visceral efferent nucleus and is the
largest parasympathetic nucleus in the brainstem. Most (80%) of its
neurones give rise to the preganglionic parasympathetic fibres of the
vagus nerve. The remainder are interneurones or project centrally. The
vagal nucleus innervates the non-striated (smooth, cardiac) muscle of
the viscera of the thorax (heart, bronchi, lungs and oesophagus) and
abdomen (stomach, liver, pancreas, spleen, small intestine and proximal part of the colon), and glandular epithelium. Neurones within the
nucleus are heterogeneous and can be classified into nine subnuclei,
which are regionally grouped into rostral, intermediate and caudal divisions. Topographic maps of visceral representation in animals suggest
that the heart and lungs are represented in the caudal and lateral part
of the nucleus, the stomach and pancreas in intermediate regions, and
the remaining abdominal organs in the rostral and medial part of the
nucleus.
There is a sparse sensory afferent supply, which arises in the nodose
ganglion and projects directly to the nucleus and possibly beyond into
the nucleus tractus solitarius.
Hypoglossal nucleus
The prominent hypoglossal nucleus lies near the midline in the dorsal
medullary grey matter. It is approximately 2 cm long. Its rostral part lies
beneath the hypoglossal trigone in the floor of the fourth ventricle (see
Fig. 21.5) and its caudal part extends into the closed part of the medulla.
The hypoglossal nucleus consists of large motor neurones interspersed with myelinated fibres. It is organized into dorsal and ventral
nuclear tiers, each divisible into medial and lateral subnuclei. There is
a musculotopic organization of motor neurones within the nuclei that
corresponds to the structural and functional divisions of tongue musculature. Thus, motor neurones innervating tongue retrusor muscles are
located in dorsal/dorsolateral subnuclei, whereas motor neurones
innervating the main tongue protrusor muscle are located in ventral/
ventromedial regions of the nucleus. Although relatively little is known
about the organization of motor neurones innervating the intrinsic
muscles of the tongue, experimental evidence suggests that motor neurones of the medial division of the hypoglossal nucleus innervate
tongue muscles that are orientated in planes transverse to the long axis
of the tongue (transverse and vertical intrinsics and genioglossus),
whereas motor neurones of the lateral division innervate tongue
muscles that are orientated parallel to this axis (styloglossus, hyoglossus, superior and inferior longitudinal).
Hypoglossal fibres emerge ventrally from their nucleus, traverse the
reticular formation lateral to the medial lemniscus, pass medial to the
inferior olivary nuclei, and curve laterally to emerge as a linear series of
10ā15 rootlets in the ventrolateral sulcus between the pyramid and
olivary eminence (see Fig. 21.8).
The hypoglossal nucleus receives corticonuclear fibres from the precentral gyrus and adjacent areas of predominately the contralateral
hemisphere. They synapse either on motor neurones of the nucleus
directly or on interneurones. Evidence indicates that the most medial
hypoglossal subnuclei may receive projections from both hemispheres.
The nucleus may connect with the cerebellum via adjacent perihypoglossal nuclei, and perhaps also with the medullary reticular formation, the trigeminal sensory nuclei and the nucleus solitarius.
Inferior olivary nucleus
The olivary nuclear complex consists of a large principal olivary nucleus
and smaller medial accessory and dorsal accessory olivary nuclei (see
Figs 21.8, 21.10). They are also precerebellar nuclei, a group that
includes the pontine, arcuate, vestibular, reticulocerebellar and spinocerebellar nuclei, all of which receive afferents from specific sources and
project to the cerebellum. The inferior olivary nucleus contains small
neurones, most of which form the olivocerebellar tract, which emerges
primarily from the hilum to run medially and intersect the medial
lemniscus (see Fig. 21.8). Its fibres cross the midline and sweep either
dorsal to, or through, the opposite olivary nuclei. They intersect the
lateral spinothalamic and rubrospinal tracts and the spinal nucleus of
the trigeminal nerve, and enter the contralateral restiform body (and
eventually the inferior cerebellar peduncle), where they constitute its
major component. Fibres from the contralateral inferior olivary complex
terminate on Purkinje cells in the cerebellum as climbing fibres; there
is a one-to-one relationship between Purkinje cells and neurones in the
complex (Nieuwenhuys et al 2008). Afferent connections to the inferior
olivary nuclei are both ascending and descending. Ascending fibres,
Nucleus solitarius
The nucleus solitarius (solitary nucleus, nucleus of the solitary tract)
lies lateral or ventrolateral to the vagal nucleus (see Fig. 21.8). A neuronal group ventrolateral to the nucleus solitarius has been termed the
nucleus parasolitarius. The nucleus solitarius is intimately related to,
and receives fibres from, the tractus solitarius, which carries afferent
fibres from the facial, glossopharyngeal and vagus nerves (Ciriello 1983,
Haines 2013, Hamilton and Norgren 1984). These fibres enter the tract
in descending order and convey gustatory information from the lingual
and palatal mucosa. They may also convey visceral impulses from the
pharynx (glossopharyngeal and vagus) and from the oesophagus and
abdominal alimentary canal (vagus). There is some overlap in this vertical representation.
The nucleus solitarius is thought to project to the sensory thalamus
and thence to the cerebral cortex (Hamilton and Norgren 1984). It may
also project to the upper levels of the spinal cord through a solitariospinal tract. Secondary gustatory axons cross the midline. Many subsequently ascend the brainstem in association with the medial lemniscus
and synapse on the most medial neurones of the ventral posteromedial
thalamic nucleus (in a region sometimes termed the accessory arcuate
nucleus). Axons from the ventral posteromedial nucleus radiate through
the internal capsule to the anteroinferior area of the sensoryāmotor
cortex and the insula. It is thought that other ascending paths end in a
number of the hypothalamic nuclei, and so mediate the route by which
gustatory information may reach the limbic system and allow appropriate autonomic reactions to be made.
Nucleus ambiguus
The nucleus ambiguus is a group of large motor neurones, situated deep
in the medullary reticular formation (see Fig. 21.10). It extends rostrally
as far as the upper end of the vagal nucleus, while caudally it is in line
with, but is not continuous with, the nucleus of the accessory nerve.
Fibres emerging from it pass dorsomedially, then curve laterally. Rostral
fibres join the glossopharyngeal nerve. Caudal fibres join the vagus and
are distributed to the pharyngeal constrictors, intrinsic laryngeal muscles
and striated muscles of the palate and upper oesophagus.
The nucleus ambiguus receives corticonuclear fibres bilaterally with
a contralateral preponderance and is connected to many brainstem
centres. At its upper end, a small retrofacial nucleus intervenes between
it and the facial nucleus. Although the nucleus ambiguus is generally
regarded as a special visceral efferent nucleus, it is also a reputed source
of general visceral efferent fibres to the vagus.
Swallowing and gag reflexes
Swallowing is initiated when food or liquid stimulates sensory nerves
in the oropharynx and is usually regarded as programmed motor behaviour rather than a reflex. The patterning and timing of striated muscle
contraction that occur in the pharynx, larynx and oesophagus during
swallowing are generated in the brainstem in a network of neural circuits. The afferent limb is the glossopharyngeal nerve: information is
relayed via the nucleus solitarius to the nucleus ambiguus, which contains the motor neurones innervating the muscles of the palate, pharynx
and larynx. If stimulation of the oropharynx occurs other than during
swallowing, a gag reflex may be initiated. There is a reflex contraction
of the muscles of the pharynx, soft palate and fauces that, if extreme,
may result in retching and vomiting.
Cough and sneeze reflexes
The cough reflex is normally initiated by irritation of tracheal or laryngeal mucosae: there is evidence of both mechanosensing and chemosensing cough receptors (McGarvey 2014). Coughing involves a
sequence of coordinated events that produce the profound change in
breathing pattern needed to expel an irritant from the lower airway.
Rapid inspiration is followed by an expiratory effort against a closed
glottis, the rapid generation of intrapulmonary pressure and the sudden
opening of the glottis and contraction of intercostal and abdominal
wall muscles, collectively producing a high-velocity flow of expired air
that sweeps irritant material up towards the pharynx in a forceful exhalation (cough). Laryngeal branches of the vagus nerve carrying general
visceral afferent information (with cell bodies in the inferior vagal
ganglion) terminate in the nucleus of the solitary tract. Second-order
neurones project to medullary respiratory centres (including a putative
cough centre) and to the nucleus ambiguus, recruiting motor neurones
innervating pharyngeal, laryngeal, diaphragmatic, intercostal and abdominal muscles
Stimulation of nasal mucosa by physical or chemical irritants initiates a sneezing reflex. Afferent impulses travel via the ethmoidal and maxillary nerves to the spinal nucleus of the trigeminal nerve. Interneurones project to the nucleus ambiguus and a putative āsneezing centreā in the rostral dorsolateral medulla (Seijo-MartĆnez et al 2006). Recruitment of a critical number of inspiratory and expiratory neurones initiates a sneeze, which involves eye closing and deep inspiration, followed by explosive exhalation as described above. If the oropharyngeal isthmus is closed by the action of palatoglossus, the air flow is diverted through the nasal cavity; otherwise the stream of expelled air flows through both oral and nasal cavities.
: Functional classification of cranial nerve nuclei. The upper figure shows the arrangement of nuclear columns in the brainstem of the embryo. The lower figure shows the nuclei derived from each column. Numbers indicate the cranial nerves connected to the nuclei (Abbreviations: SVE, special visceral efferent; GVE, general visceral efferent; GVA, general visceral afferent; SVA, special visceral afferent; GSA, general somatic afferent; SSA, special somatic afferent; SE, somatic efferent)
arises from the olfactory epithelium in the nasal cavity and
terminates directly in cortical and subcortical areas of the frontal and
temporal lobes;
Transmits sense of smell
Branches arise from sensory cells of nasal mucosa, enter cranial cavity as olfactory filament through openings of cribriform plate of ethmoid bone
Enter olfactory bulb singly
Bulb is vestigial of olfactory lobe of macrosmatic mammals.
The axons of the optic nerve
(II) pass into the optic chiasma, where medially positioned axons decussate; all of the axons emerge as the optic tract, which terminates in the lateral geniculate nucleus of the thalamus (
Second pair of cranial nerve
Nerve of visual sense
Arise in ganglion cells of retina
Enters cranial cavity through optic foramen
1 half hemianopia
Same half of both eyes homonymous
Different half heteronymous
Contains somatic & parasympathetic visceral efferent fibres
Somatic fibres responsible for most of the extrinsic muscles of the eye
Parasympathetic fibres relay in ciliary ganglion
Postganglionic fibres arising from ciliary ganglion, enter eyeball & supply ciliary muscles or muscles of accommodation & sphincter of pupil
Enters orbit through superior orbital fissure
Fixed pupil ā loss of sympathetic fibres
WEBERāS SYNDROME- A midbrain lesion causing contra lateral hemiplegia & ipsilateral paralysis of third nerve
Carries somatic fibers , motor .
supply superior oblique muscle of eyeball
/ SO 4
Passes through superior orbital fissure
Only cranial nerve that emerges from dorsal aspect of brain stem
Diplopia occurs on looking downwards
It results in defective depression of adducted nerve
Extorsion of the eyeball
Diplopia on looking downwards but single vision above horizontal plane
At meckelās cave ā apex of petrous temporal bone
1st branch of V th cranial nerve
Purely sensory & smallest of 3 divisions
Supplies eyeball, conjunctiva, lacrimal gland, parts of mucous membrane of nose & PNS & skin of forehead, eyelids & nose
Divides into 3 main branches just before passing through superior orbital fissure ā
Nasocilliary
Frontal
Lacrimal ā smallest branch
Neuropathic pain as defined by International Association for the Study of Pain is a type of pain initiated or caused by a primary lesion or dysfunction in the nervous system [1]. It is caused by neural injury or painful states associated with either peripheral or central nerve injury.
There are relatively few reports on endodontic nerve injuries which may not be limited to those teeth proximal to the IAN canal but may occur in maxillary teeth as well
Neuropathic pain (NP) syndromes are chronic pain disorders that develop after a lesion of the peripheral or central nervous structures that are normally involved in signalling pain. The characteristics of NP differ substantially from those of other chronic pain states, that is, chronic nociceptive pain, which develops while the nervous system that is involved in pain processing is intact. As well as the existence of negative somatosensory signs (deficit in function) there other definitive features that are characteristic of neuropathic conditions (allodynia, hyperalgesiaPrevention of endodontic-related neuropathy: risk factors In this cohort, there appeared to be several prominent risk factors which were as follows: ā¢ GDP (80% of referrals) ā¢ Proximity of tooth to IAN canal ā 90% of the mandibular teeth in this series were close to the IAN canal or premolars adjacent to the mental foramen ā¢ Detectable overfill occurred in 60% of cases and over instrumentation during preparation in all cases resulting in one or a combination of ā mechanical injury ā haemorrhagic/ischaemic injury ā chemical injury (Figs 1,2
Why should it be any different in dentistry? We already have the evidence that demonstrates the fact that
Mixed nerve
Contains two nerves ā facial nerve proper and intermediate nerve .
Seventh cranial nerve of second branchial arch
NUCLEI- There are 4 nuclei situated in the lower pons-
Motor nucleus or branchiomotor
Superior salivatory nucleus or parasympathetic
Lacrimatory nucleus
Nucleus of tractus solitarius
Rmsay hunt syndrome
ļ SCHIRMER TEST- decrease in lacrimation of 75% or more as compared to normal side. Or < 10mm for both sides at 5 min. ļ STAPEDIAL REFLEX TESTING - if absent , site of lesion between geniculate ganglion and stapedius muscle. If present then site of lesion is distal to stapedius muscle. ļ TASTE TESTING ā conc. Sweet, salt, sour and bitter solution tested along lateral margin of anterior 2/3 of tongue towards tip / electrogustometry ( EGM ) ļ SUBMANDIBULAR GLAND FLOW- compared by sialometry using 6% citric acid. ļ TESTING FACIAL MOVEMENT
Sensory nerve
Has two roots - vestibular and cochlear
Vestibular root : impulse from vestibular apparatus
/balance
Cochlear root : transmit impulse from auditory apparatus /sound
Function : transmit sound and equilibrium from internal ear to brain.
Rinne- base of tuning fork on the mastoid process,
ātell me when it stopsā, then bring it to the ear,
āCan hear it? ā
With nerve deafness the note is audible at the external meatus, as air and bone conduction are reduced equally, so that air conduction is better as is normal. This is termed Rinne-positive.
With conduction [middle ear] deafness no note is audible at the external meatus.
This is termed Rinne-negative
A vibrating tuning fork is placed on the centre of the forehead. Normally the sound is heard in the centre of the forehead. With nerve deafness the sound is transmitted to the normal ear. With conduction deafness the sound is heard louder in the abnormal ear.
Patients with defective hearing should be referred for audiometry. This measures the degree of hearing loss at different sound frequencies.
innitus-the perception of sound in the absence of an actual external sound-represents a symptom of an underlying condition rather than a single diseaseTreatments for tinnitus include pharmacotherapy, cognitive and behavioral therapy, sound therapy, music therapy, tinnitus retraining therapy, massage and stretching,
Intracranial course: The glossopharyngeal nerve emerges from medulla as a series of rootlets between the olive and inferior cerebellar peduncle. It traverses the posterior cranial fossa and exits through the jugular foramen. Extracranial course: The superior and inferior sensory ganglia are situated on the nerve at the exit. The glossopharyngeal nerve descends in the neck and supplies stylopharyngeus muscle. The nerve then passes between superior and middle constrictors of pharynx and supply the mucosa of the pharynx and posterior one-third of tongue.
Emerges from lateral surface of medulla oblongata & passes in front of vagus nerve through jugular foramen
Contains motor fibres
Motor supply to stylopharyngeus muscle & participates with vagus in supplying constrictors of pharynx & palatopharyngeus muscle
Sensory supply to parts of tonsil, adjacent pharyngeal mucosa , base of tongue
Taste sensation from vallate and foliate papillae
Intracranial course: The vagus nerve emerges as a series of rootlets in a groove between the olive and inferior cerebellar peduncle. It traverses the posterior cranial fossa and exits the skull through jugular foramen. The superior Figure 6.23: Vagus nerve: Origin, course and distribution (Abbreviations: SVE, special visceral efferent; GVE, general visceral efferent; SVA, special visceral afferent; GVA, general visceral afferent; GSA, general somatic afferent) sensory ganglion of the nerve is located in the jugular foramen. Extracranial course: The inferior ganglion of vagus lies just below the jugular foramen. Just below the inferior ganglion, the cranial root of accessory nerve joins the vagus nerve to be distributed along its pharyngeal and laryngeal branches. In the neck, the vagus lies in the carotid sheath along with the internal jugular vein and common carotid arteries. The right vagus passes posterior to the root of right lung, contributes to pulmonary plexus, and then runs on the posterior surface of oesophagus, contributing to the oesophageal plexus. It enters theabdomen by passing through the oesophageal opening in the diaphragm. It supplies stomach, duodenum, liver, kidneys, small and large intestine up to the junction of proximal two-thirds and distal third of transverse colon. It has a wide distribution in the abdomen via coeliac, superior mesenteric and renal plexuses. The left vagus enters thorax, contributes to pulmonary and oesophageal plexuses, then enters abdomen supplies stomach, liver, duodenum and head of pancreas.
Cricothyroid
Levator veli palatini
Salpingopharyngeus
Palatopharyngeus
Palatoglossus
Palatopharyngeus
Superior, middle , inferior pharyngeal constrictor .
Muscles of larynx
Stimulation auricular branch of vagus causes increased appetite
Cranial root : joins vagus nerve and innervates all laryngeal muscles except cricothyroid
Spinal root : innervates trapezius , SCM
This can be explained
as follows. One of the genioglossus muscles, which pull the
tongue forward, is paralyzed on the affected side. The other,
normal genioglossus muscle pulls the unaffected side of the
tongue forward, leaving the paralyzed side of the tongue stationary. The result is the tip of the tongueās deviation toward
the paralyzed side. In patients with long-standing paralysis,
the muscles on the affected side are wasted, and the tongue
is wrinkled on that side