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AUTONOMIC NERVOUS SYSTEMANATOMY PHYSIOLOGY AND DYSFUNCTION

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RICHA GUPTA MPT II YR

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Introductiony Involuntary AND automatic nervous system y Primarily concerned with regulation of visceral or

vegetative functions

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Autonomic Nervous System

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DIVISIONS OF ANS

Sympathetic

ANS

Parasympathetic

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THIRD DIVISION OF ANS

ENTERIC NERVOUS SYSTEM

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SYMPATHETIC DIVISIONy Thoracolumbar outflow y Preganglionic neurons: LGH of 12 thoracic & 2 lumbar

segments of SCy Preganglionic fibers

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Sympathetic ganglia

Paravertebral

Prevertebral

Terminal or Peripheral

Heart, Bronchi, pancreas, bladder

cervical Thoracic

Lumbar & sacral Sup. mesenteric Inf. mesenteric

Celiac

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PARASYMPATHETIC DIVISIONy CRANIOSACRAL OUTFLOW

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PARASYMPATHETIC DIVISION

Tectal or midbrain level

Bulbar level or bulbar outflow

Sacral outflow

Edinger Westphal Nucleus of CN III

VII, IX & X CN fibers

2, 3 & 4th sacral segment

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Functions of ANSy Regulation of functions which are beyond voluntary control y Maintain homeostasis y SNS & PNS antagonistic effect

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y Governs activities of cardiac & smooth muscles including

smooth muscles of blood vessels & glandular functiony Regulates respiration, circulation, digestion, temp

adjustment & metabolism

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Sympathetic Divisiony Stress responsesy Increased pulse & respiratory rate y Vasoconstriction to skin & viscera y Sweating (cold sweat) y Release of "adrenalin (epinephrine) y Inhibition of digestive activity y Loss of appetite

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Parasympathetic Divisiony Relaxation responsesy y y y

Slower pulse & respiratory rate Increased blood flow to skin & viscera Increased digestive activity SLUDy Salivation, Lacrimation, Urination, Digestion/Defecation

y Increased reproductive interest, receptiveness y Penile erection, engorgement of vulva

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No. 1. 2. 3. 4.

Effector organ Eye Ciliary muscle Pupil Lacrimal glands Salivary secretion GIT- Motility Secretion Sphincters Gall bladder Urinary bladder- Detrusor Internal sphincter Sweat glands Heart- rate & Force of contraction Blood vessels- skin coronary ANS.ppt skeletal msl

Sympathetic Relaxation Dilatation Decrease in secretion Decrease Inhibition Decrease Constriction Relaxation Relaxation Constriction Increase secretion Increase Increase Constriction Dilalatation Constriction

Parasympathetic Contraction Constriction Increase Increase Acceleration Increase Relaxation Contraction Contraction Relaxation Decrease Decrease No effect No effect No effect No effect8/6/2011

5. 6. 7. 8. 9.17

NO. 10.

EFFECTOR ORGAN LUNGS: Bronchiole Gland secretion

SYMPETHETIC

PARASYMPETHETIC

Dilatation Decrease

Constriction Increase

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Reproductive system: Male sex organs External genitalia Mucous membrane

Ejaculation No action on BVs Capillaries constricted, Decreased mucous secretion

No action dialatation No action

12.

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DETAILED ANATOMY

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Autonomic Nervous System:Anatomyy Two kinds of efferent neurons y Preganglionic neuron/axony Cell body in CNS, axon to autonomic ganglion (usu. myelinated)

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y Ganglionic neuron y Cell body in ganglion, postganglionic axon to effector y (unmyelinated)

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Parasympathetic: Anatomyy Ganglia y Terminal, = intramural gangliay in walls of viscera, close to effector cells

y Preganglionic axons relatively long

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PARASYMPATHETIC NERVOUS SYSTEMy

PREGANGLIONIC NEURONS:

Located partly in the brain stem in connection with: 3rd(occulomotor) 7th(facial) 9th(glossophyrangeal) and 10th(vagus) . And partly in the 2nd,3rd & 4th sacral segment of spinal cord. Hence called craniosacral outflow.

Parasympathetic:Anatomyy Parasympathetic pathway y Hypothalamus & brain stem y Cranial or sacral outflow y Long preganglionic axon to intramural ganglion y Short ganglionic neuron (postganglionic axon)

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y POST GANGLIONIC NEURONS: Occulomotor nerve are situated in the ciliary

ganglion. Facial nerve in pterygopalantine and submandibular ganlion. Glossopharyngeal nerve in the otic ganglia. Vagus and sacral component are loacated in the walls of target organs.

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Sympathetic:Anatomy y Sympathetic Ganglia1.Sympathetic trunk = sympathetic chain ganglia paired on either side of vertebrae 2.Prevertebral = collateral ganglia unpaired among abdominal viscera y Celiac ganglion y Superior mesenteric ganglion y Inf. mesenteric ganglion y Aortico-renal y Superior hypogastric 3.Terminal or peripheral ganglia Suprarenal medulla as chromaffin cells27 ANS.ppt 8/6/2011

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Sympathetic Trunk Ganglia

Figure 15.8

y The trunk presents: 3 ganglia in cervical part ie superior,

middle and

inferior 11 ganglia in thoracic part 4 ganglia in lumbar part 4 ganglia in sacral part

y some time inferior cervical and first thoracic ganglia are

fused to form a cervicothoracic or stellate ganglia. y Upper 4 cervical ganglia are fused to form the sup. Cervical ganglion, 5th and 6th unite to form middle cervical ganglion y 7th and 8th cervical ganglion join to form inf. Cervical ganglion.

y Each of thoracic and upper two lumbar sympathetic

ganglion is connected to the corresponding spinal nerves by both white and gray rami communicants, white rami lying lateral to the gray rami. White rami: convey preganglionic fibers from lateral horn cells of T1-L2 segment of spinal cord through all thoracic and upper two lumbar spinal nerves.Grey rami: convey post ganglionic fibers from the lateral ganglia through all 31 pairs of spinal nerves and their limb plexuses to supply sudomotor, pilomotor and vasoconstrictor fibers to segmental skin viscera of body wall, upper and lower limb and and vasodilator fibers to the skeletal muscle.35 ANS.ppt 8/6/2011

Subsidiary ganglia: consist of collateral and terminal ganglia. Collateral ganglia: are represented by coeliac,superior mesenteric, inferior mesenteric, aortico renal ganglia and neurons in the sup. Hypogastric plexus. Terminal ganglia: are formed only in the suprarenal medulla as the chromaffin cells which liberate more adrenalin than non adrenaline.

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Sympathetic:Anatomyy Adrenal medulla y One in each adrenal gland y Develops as misplaced sympathetic ganglion y Neuron-like cells without axons y Secrete epinephrine, norepinephrine

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s.no.

characterestic

SNS

PNS

1.

Origin

T1 to L2-L3 Thoracolumbar outflow Situated away from the organ it supply Short

Cr ns. III,VII, IX, X Sacral. S2, S3, S4 Craniosacral outflow Situated near or at the organ it supply Long

2.

Ganglia

3.

Preganglionic fibres

4.

Postganglionic fibers

Long

Short

5.

Neurotransmitters

Presynaptic- Ach Postsynaptic- nor adrenaline

Both Ach

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AUTONOMIC DYSFUNCTION

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y Acute autonomic paralysis ( dysautonomic polyneuropathy;

pure pandysautonomia)y Primary autonomic failure ( idiopathic orthostatic

hypotension )y Peripheral neuropathy with secondary orthostatic

hypotension

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y Autonomic neuropathy in infants & children (Riley-Day

Syndrome)y Autonomic failure in elderly y Horner (oculosympathetic) & stellate ganglion syndromes

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y Sympathetic & Para sympathetic paralysis in Tetraplegia &

Paraplegiay Acute autonomic crisis ( Sympathetic Storm ) y Disorders of sweating y Disturbances of bladder & bowel function

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ANS dysfunction following SCI

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Journal of Rehabilitation Research & Development. 2007

y Assessment of autonomic dysfunction following spinal cord

injury: Rationale for additions to International Standards for Neurological Assessmentjoint committee of the American Spinal Injury Association (ASIA) and the International Spinal Cord Society

The committee recommends The recognition and assessment of the following conditions: neurogenic shock, cardiac dysrhythmias, orthostatic hypotension, autonomic dysreflexia, temperature dysregulation, and hyperhidrosis.

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Neurogenic shocky Severe hypotension and bradycardia y An effect of the imbalance in autonomic control, with an

intact parasympathetic influence via the vagal nerve and a loss of sympathetic tone because of disruption in supraspinal control

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y Can last upto 5 weeks post injury y Spinal shock

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Cardiac Dysrhythmiasy Depends on level & completeness of SCI y Above T6:

reduction in sympathetic cardiovascular control hypotension & bradycardia. Usually temporary

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Orthostatic Hypotensiony A decrease in systolic blood pressure of 20 mmHg or a

decrease in diastolic blood pressure of 10 mmHg when the subject moves from an supine to upright posture, regardless of whether symptoms occur.Consensus Committee of the American Autonomic Society and the American Academy of Neurology

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y Loss of supraspinal control of the sympathetic nervous

system below the lesion level frequently results in orthostatic hypotensiony 2 grades of severity: Asymptomatic

Symptomatic

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y Symptoms : dizziness, nausea, light-headedness, or faintness y Physical signs : pallor, diaphoresis, or loss of consciousness y Common problem after acute cervical and high thoracic SCI

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MechanismInterruption of efferent pathways from the brain stem vasomotor center to the sympathetic nerves involved in vasoconstriction

Failure of short-term blood pressure regulation

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Pooling of blood in the viscera and dependent vasculature

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Autonomic Dysreflexiay Sudden bouts of hypertension (triggered by afferent stimuli

below the lesion level)y Accompanied by piloerection, chills or shivering, pounding

headache, paresthesias & flushing above the lesion level, as well as nasal congestion, anxiety, malaise, and nausea

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y In both acute & later stages y Occurs as a result of noxious or nonnoxious peripheral or

visceral stimulation below the lesion levely Primarily affects subjects with lesions above the outflow to

the splanchnic and renal vascular beds (T5T6)

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y Found in subjects with both complete and incomplete lesions

(C>I)y Irritation of the urinary bladder and GIT are among the most

common causes

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Temperature Dysregulationy Occurs in the acute phase of SCI and can potentially last a

lifetimey 3 categories Poikilothermia, or environmental fever, from prolonged

cold exposure Quad fever without an infectious source Exercise-induced fever

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Sweating Disturbancesy Hyperhidrosis y Most common pattern: profuse sweating above the lesion

level with minimal or no sweating (hypohidrosis, anhidrosis) below the lesion level

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International Standards for Neurological Classification of Spinal Cord Injury: Training Effect on Accurate Classification

J Spinal Cord Med. 2008;31:538542

The International Standards for Neurological Classification of Spinal Cord Injury: Intra-Rater Agreement of Total Motor and Sensory Scores in the Pediatric Population J Spinal Cord Med. Apr 2009;32(2):157161

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Autonomic Peripheral NeuropathyRoy Freeman Neurol Clin 25 (2007) 277301

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y Small or Unmyelinated fibers are selectively involved.

S/S y Cardiovascular y Thermoregulatory y Gastrointestinal y Urogenital y Pseudomotor y Pupillomotor

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Diabetic autonomic neuropathyy Manifests initially as an increased resting heart rate caused by

a cardiac vagal neuropathy y Later on, sympathetic involvementy Orthostatic hypotension occurs in diabetes as a consequence

of efferent sympathetic vasomotor denervation, causing reduced vasoconstriction of the splanchnic and other peripheral vascular beds

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y Bladder dysfunction: threshold for micturition reflex is increased y GI Dysfn: diabetic gastroperesis y Constipation y Diabetic diarrhoea y Loss of thermoregulatory sweating in a glove and stocking

distribution: SNS dysfn y Hyperhydrosis

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Guillain-Barre syndrome

y Orthostatic hypotension

y Thermoregulatory problems

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Cardiovascular manifestation of autonomic involvement Sinus tachycardia Bradycardia Asystole Tachyarrhythmias( fibrillation, flutter) ECG changes (elevated or depressed ST segment changes, QT interval prolongation) y Postural hypotension y Hypertensiony y y y y y

Riley-Day-Syndrome (familial dysautonomia)y This syndrome has an autosomal recessive mode of

inheritance and occurs primarily in Ashkenazic jewsy Pathological studies show reduction in number of

preganglionic neurons in intermediolateral columns and also small myelinated fibers in the ventral roots.

y Clinical features: y Diminished lacrimation y Hyperhydrosis y Transient blotching of skin y Postural hypotension y Poor temperature control

Autonomic Dysfunction in PD

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y Occur in 90% patients during disease course y May be the result of other conditions (such as multiple

system atrophy [MSA]), the aging process itself, or pharmacotherapy for PD

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Multiple System Atrophyy It is a degenerative disease with onset in middle of life. Clinically characterised by any combination of Parkinsonian, autonomic, pyramidal or cerebellar symptoms

and signs.

y Autonomic featuresy Postural faintness y Recurrent syncope y Urinary incontinence y Faecal incontinence y Impotence in males

Localised Dysautonomic DisorderHorners syndrome Lesion affecting pre ganglionic fibres from T1 and T2 at the inferior cervical gangion is manifested by horners syndrome. Clinical features: y Ptosis y Miosis y Anhidrosis y Enophthalmos1.

y Pre ganglionic lesion : Thoracic surgical trauma Trauma to brachial plexus Aneurysm of aorta or subclavian artery

Post ganglionic lesion : Ischemia or compression of paracarotid sympathetic pathways as a result of vasospasm

Holmes Adie Syndromey Pupil has decreased or absent light reflex y A slow or delayed contraction to near vision y And slow or delayed dilatation to dark

Causes y Degeneration of the ciliary ganglion and the post ganglionic parasympathetic fibers of constrictor pupillae muscle

Hirschsprungs diseasey Congenital y Absence of myentric plexus y Segment of colon remain in constriction

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Raynauds Diseasey Raynauds disease characterized by constriction of blood vesselsy Provoked by exposure to cold or by emotional stress

Hypertensiony Hypertension high blood pressurey Can result from overactive sympathetic vasoconstriction

AUTONOMIC DYSFUNCTION AFTER TBI???

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Dysautonomia after severe traumatic brain injuryEuropean Journal of Neurology 2010, 17: 1172-1177 INCIDENCE: 11.8% Dysautonomia after traumatic brain injury (TBI) is characterized by episodes of increased heart rate, respiratory rate, temperature, blood pressure, muscle tone, decorticate or decerebrate posturing, and profuse sweating.

PATHOGENESIS: Epileptogenic etiology Disconnection theory Excitation- inhibition ratio model

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THANK YOU

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