Unit 17 — Autonomic Nervous System · Question Bank

TMU Anatomy · Sympathetic · Parasympathetic · Visceral Nerves · Referred Pain
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Q1
The lower nervous centres (lateral grey horn cell bodies) of the sympathetic division are located at:
TMU Slide 10
A. T1–L2 (thoracolumbar)
B. C1–C8
C. S2–S4 (sacral)
D. T1–T12 only
✓ Answer: A — T1–L2 thoracolumbar outflow
The sympathetic division is the thoracolumbar outflow. Preganglionic cell bodies lie in the lateral grey horn of spinal cord segments T1 to L2 (some sources cite T1 or C8 to L2 or L3). This is why sympathetic effects can be described as “thoracolumbar” — the fibres exit with the corresponding spinal nerves via the white rami communicantes.
⚠ C = sacral outflow of parasympathetic (S2–S4), not sympathetic. D = thoracic only would miss the lumbar ganglia. Memorise: Sympathetic = Thoracolumbar; Parasympathetic = Craniosacral.
Q2
Which of the following correctly describes the parasympathetic (craniosacral) outflow?
TMU Slide 24–25
A. CN I, V, X and S1–S3
B. CN III, VII, IX, X and S2–S4
C. CN III, VII, IX, X and S1–S3
D. CN V, VII, IX, X and S2–S4
✓ Answer: B — CN III, VII, IX, X + S2–S4
The cranial component carries parasympathetic fibres in four cranial nerves: CN III (oculomotor), CN VII (facial), CN IX (glossopharyngeal), CN X (vagus). The sacral component exits as pelvic splanchnic nerves from S2–S4. This is the craniosacral outflow — the “rest-and-digest” system.
⚠ CN I = olfactory (sensory only). CN V = trigeminal (mainly sensory; carries parasympathetic fibres to end organs but does not carry its own preganglionic parasympathetics). The four cranial nerves with parasympathetics: 3, 7, 9, 10.
Q3
Sympathetic postganglionic fibres are correctly described as:
TMU Slides 3, 33
A. Long, myelinated, release acetylcholine
B. Short, myelinated, release noradrenaline
C. Long, unmyelinated, release noradrenaline
D. Short, unmyelinated, release acetylcholine
✓ Answer: C — Long, unmyelinated, noradrenaline
In the sympathetic division: preganglionic fibres are short, myelinated, and release ACh (at the ganglion). Postganglionic fibres are long, unmyelinated, and release noradrenaline (at the target organ). The ganglion is located near the spinal cord (paravertebral or prevertebral), so postganglionic fibres must travel a long distance to reach the end organ.
⚠ The classic exam trick: A = preganglionic parasympathetic (long myelinated ACh). D = postganglionic parasympathetic (short unmyelinated ACh). Exception: sympathetic postganglionic fibres to sweat glands are also cholinergic (ACh) despite being sympathetic.
Q4
Parasympathetic postganglionic fibres are correctly described as:
TMU Slides 3, 33
A. Long, unmyelinated, release noradrenaline
B. Short, myelinated, release acetylcholine
C. Long, myelinated, release acetylcholine
D. Short, unmyelinated, release acetylcholine
✓ Answer: D — Short, unmyelinated, acetylcholine
In the parasympathetic division: preganglionic fibres are long, myelinated, and release ACh (ganglion is close to or within the target organ). Postganglionic fibres are short, unmyelinated, and also release ACh. The parasympathetic system is entirely cholinergic (ACh at both synapses). Receptors on end organs are muscarinic.
⚠ Both preganglionic and postganglionic parasympathetics release ACh. Contrast with sympathetics: pre = ACh (nicotinic), post = noradrenaline (adrenergic) — except sweat glands. Parasympathetic postganglionic = SHORT because ganglia are near/in the wall of target organs.
Q5
Sweat glands are innervated by sympathetic postganglionic fibres that release:
TMU Slide 33 exception
A. Acetylcholine (cholinergic exception)
B. Noradrenaline (adrenergic)
C. Adrenaline (epinephrine)
D. Dopamine
✓ Answer: A — Acetylcholine (the sympathetic ACh exception)
Sweat glands are the classic exception to the rule that sympathetic postganglionic fibres release noradrenaline. Sweat glands are innervated by sympathetic postganglionic cholinergic fibres (release ACh). They are structurally sympathetic (arise from sympathetic chain ganglia, part of sympathetic chain) but are functionally cholinergic. Muscarinic ACh receptors mediate sweating.
⚠ High-yield exception. In exams: “sympathetic but cholinergic” = sweat glands (and some vasodilator fibres to skeletal muscle). In Horner's syndrome, anhidrosis (loss of sweating) on the ipsilateral face/neck is due to loss of sympathetic (cholinergic) supply to facial sweat glands.
Q6
The adrenal medulla secretes catecholamines when stimulated by:
TMU Slide 33
A. Postganglionic sympathetic fibres (noradrenergic)
B. Preganglionic sympathetic fibres (cholinergic) directly
C. Postganglionic parasympathetic fibres (cholinergic)
D. Somatic motor fibres
✓ Answer: B — Preganglionic sympathetic directly
The adrenal medulla is a modified postganglionic sympathetic ganglion (developmentally derived from neural crest cells). It is stimulated directly by preganglionic sympathetic fibres (short, myelinated, cholinergic) without synapsing at a separate ganglion. The chromaffin cells of the medulla are the equivalent of postganglionic neurons — they release adrenaline (80%) + noradrenaline (20%) into the bloodstream, acting as a hormonal amplifier of the sympathetic response.
⚠ Key concept: adrenal medulla = modified postganglionic neuron = directly innervated by preganglionic (skips a synapse). This is why the adrenal medullary response can be triggered rapidly during “fight-or-flight” without an extra synaptic relay.
Q7
The greater splanchnic nerve is formed by preganglionic sympathetic fibres from spinal segments:
TMU Slides 17–18
A. T1–T4 → heart and lungs
B. T10–T11 → superior mesenteric ganglion
C. T5–T9 → coeliac ganglion
D. T12 → renal plexus
✓ Answer: C — T5–T9 to coeliac ganglion
The greater splanchnic nerve is formed by preganglionic fibres from T5 to T9 (from thoracic sympathetic chain ganglia 5–9). It passes through the diaphragm to synapse in the coeliac ganglion (prevertebral). Postganglionic fibres from the coeliac ganglion supply the foregut and associated structures. It also carries preganglionic fibres directly to the adrenal medulla.
⚠ Mnemonic for splanchnic levels: Greater = 5–9 → Coeliac; Lesser = 10–11 → SMA ganglion; Least = 12 → Renal plexus. Greater is the largest and most clinically important (targeted in splanchnic nerve block for pancreatic pain).
Q8
The lesser splanchnic nerve (T10–T11) synapses in which ganglion?
TMU Slide 17
A. Coeliac ganglion
B. Inferior mesenteric ganglion
C. Aorticorenal ganglion
D. Superior mesenteric ganglion
✓ Answer: D — Superior mesenteric ganglion
The lesser splanchnic nerve (T10–T11) passes through the diaphragm and synapses in the superior mesenteric ganglion (prevertebral ganglion at the origin of the superior mesenteric artery). Postganglionic fibres supply the midgut (small intestine, ascending colon, transverse colon). Some fibres also go to the aorticorenal ganglion.
⚠ The three splanchnic nerves and their targets: Greater (T5–9) → coeliac ganglion → foregut; Lesser (T10–11) → SMA ganglion → midgut; Least (T12) → renal plexus → kidney/ureter. Don't confuse with the inferior mesenteric ganglion (receives lumbar splanchnic L1–L2 fibres, supplies hindgut).
Q9
The vagus nerve (CN X) provides parasympathetic innervation to the GI tract as far as the:
TMU Slide 25; Gray's 4e
A. Left colic (splenic) flexure
B. Ileocaecal junction
C. Sigmoid colon
D. Rectum
✓ Answer: A — Left colic (splenic) flexure
The vagus nerve (CN X) supplies parasympathetic innervation to the heart, lungs, oesophagus, stomach, small intestine, and large intestine up to and including the left colic (splenic) flexure. This boundary corresponds exactly to the SMA/IMA vascular watershed. Beyond the splenic flexure (descending colon, sigmoid, rectum, bladder, genitalia), parasympathetics come from the pelvic splanchnic nerves (S2–S4).
⚠ High-yield boundary: vagus = up to splenic flexure; pelvic splanchnics = beyond splenic flexure. This matches the embryological midgut/hindgut boundary. In surgery: left colon procedures can affect pelvic parasympathetic pathways differently from right colon.
Q10
CN III (oculomotor nerve) carries parasympathetic fibres to the ciliary ganglion. What are the effects of the postganglionic fibres from this ganglion?
TMU Slide 25; Gray's 4e
A. Pupil dilation (mydriasis) + lens relaxation
B. Pupil constriction (miosis) + lens thickening for near vision (accommodation)
C. Pupil constriction only; no effect on lens
D. Lens thickening only; pupil size unchanged
✓ Answer: B — Miosis + accommodation
Preganglionic parasympathetic fibres from CN III synapse in the ciliary ganglion (located in the orbit). Short postganglionic fibres supply two smooth muscles: (1) Sphincter pupillae → pupil constriction (miosis); (2) Ciliary muscle → contraction relaxes the suspensory ligament (zonule) → lens rounds up/thickens → accommodation for near vision. These two responses together form the near reflex triad (convergence + accommodation + miosis).
⚠ A = sympathetic effects (pupil dilation via dilator pupillae + lens flattening for distance vision via ciliary muscle relaxation). In CN III palsy: dilated, non-reactive pupil (loss of parasympathetic sphincter pupillae) + no accommodation. Compare Horner's: loss of sympathetic → miosis + ptosis + anhydrosis.
Q11
CN VII (facial nerve) carries parasympathetic fibres to two ganglia. Which glands do these ganglia supply?
TMU Slide 25; Gray's 4e
A. Pterygopalatine ganglion → parotid; submandibular ganglion → lacrimal
B. Otic ganglion → parotid; ciliary ganglion → lacrimal + nasal
C. Pterygopalatine ganglion → lacrimal + nasal glands; submandibular ganglion → sublingual + submandibular glands
D. Pterygopalatine ganglion → submandibular; otic ganglion → sublingual
✓ Answer: C — Pterygopalatine → lacrimal/nasal; submandibular → sublingual/submandibular
CN VII (facial) carries parasympathetic fibres in two divisions: (1) Greater petrosal nerve → pterygopalatine ganglion → lacrimal gland + nasal mucosa + palate glands (secretomotor); (2) Chorda tympani → lingual nerve → submandibular ganglion → sublingual gland + submandibular gland (secretomotor). The chorda tympani also carries taste from the anterior 2/3 of the tongue.
⚠ A = the otic ganglion is CN IX territory (parotid gland). Mnemonic: CN VII = two ganglia: PPG (lacrimal/nasal) + SMG (sublingual/submandibular); CN IX = one ganglion: otic (parotid). Dry eye (keratoconjunctivitis sicca) can result from lesions interrupting the greater petrosal branch of CN VII.
Q12
CN IX (glossopharyngeal nerve) carries preganglionic parasympathetic fibres via the lesser petrosal nerve to the otic ganglion. The postganglionic fibres supply:
TMU Slide 25; Gray's 4e
A. Sublingual and submandibular salivary glands
B. Lacrimal gland and nasal mucosa
C. Ciliary muscle and sphincter pupillae
D. Parotid gland (secretomotor)
✓ Answer: D — Parotid gland
CN IX → tympanic nerve → tympanic plexus → lesser petrosal nerve → otic ganglion (below foramen ovale in infratemporal fossa) → postganglionic fibres join the auriculotemporal nerve (branch of CN V3) → parotid gland (secretomotor). Clinical: Frey's syndrome (auriculotemporal nerve damage during parotidectomy → aberrant reinnervation of sweat glands → gustatory sweating).
⚠ The four cranial parasympathetic ganglia and their cranial nerve: ciliary = CN III; pterygopalatine = CN VII; submandibular = CN VII; otic = CN IX. All four ganglia “hitch-hike” on branches of CN V (trigeminal) to reach their target organs.
Q13
The pelvic splanchnic nerves (S2–S4) provide parasympathetic supply to all of the following EXCEPT:
TMU Slide 28; Gray's 4e
A. Parotid gland
B. Descending and sigmoid colon
C. Urinary bladder (detrusor muscle)
D. Erectile tissue of the penis/clitoris
✓ Answer: A — Parotid gland is CN IX / otic ganglion territory
Pelvic splanchnic nerves (S2–S4) supply: descending colon, sigmoid colon, rectum (hindgut beyond splenic flexure); urinary bladder (detrusor — mediates micturition); genitalia (erectile tissue — mediates erection via “VIP + NO” vasodilation). The parotid gland is supplied by the otic ganglion → CN IX, entirely separate from pelvic outflow.
⚠ Erection = parasympathetic (pelvic splanchnics, “point”); ejaculation = sympathetic (hypogastric nerve, “shoot”). S2–S4 injury (e.g. cauda equina) → loss of erection + bladder dysfunction + saddle anaesthesia.
Q14
A patient with acute myocardial infarction complains of severe pain radiating to the left arm and jaw. The anatomical basis for this referred pain is that cardiac afferent fibres converge on spinal cord levels:
TMU Slide 39; Gray's 4e
A. C3–C5 (phrenic nerve territory)
B. T1–T5 dermatomes (left arm + chest)
C. T6–T10 (abdominal dermatomes)
D. L1–L2 (groin dermatomes)
✓ Answer: B — T1–T5 dermatomes
Cardiac pain is referred because visceral afferents from the heart travel with sympathetic fibres and enter the spinal cord at T1–T5. These levels share spinal neurons with somatic afferents from the medial left arm (T1–T2) and precordium (T2–T5). The brain misinterprets the signal as coming from the skin → pain is “felt” in the left arm and jaw. The jaw component relates to higher cervical referral via the cardiac plexus.
⚠ C3–C5 = diaphragmatic irritation refers to the shoulder tip (phrenic nerve = C3–C5). Cardiac pain is specifically T1–T5. Right-sided MI can refer to the right arm. Silent MI (no pain) is common in diabetics due to autonomic neuropathy affecting afferent fibres.
Q15
In acute appendicitis, the pain classically migrates from the periumbilical region to the right iliac fossa (RIF) because:
TMU Slides 38–39; Gray's 4e
A. The appendix moves from the umbilicus to RIF as inflammation progresses
B. The mesenteric lymph nodes enlarge from umbilicus towards RIF
C. Initial visceral pain is referred to T10 dermatome (periumbilical); later parietal peritoneum irritation gives somatic pain localised to RIF
D. T10 afferents only carry temperature sensation, not pain
✓ Answer: C — Visceral T10 referred pain → somatic localisation to RIF
Phase 1 (early): appendiceal visceral afferents enter at T10 → referred pain felt at the periumbilical region (T10 dermatome = umbilicus level). Pain is dull, diffuse, poorly localised (visceral). Phase 2 (as inflammation spreads to parietal peritoneum): somatic afferents (via iliohypogastric/ilioinguinal nerves, L1) and lower thoracic intercostals are activated → sharp, well-localised pain at RIF / McBurney's point. Rebound tenderness = sign of parietal peritoneal irritation.
⚠ Classic clinical question. Visceral pain = vague, midline, referred; somatic = sharp, localised, associated with guarding and rebound. Rovsing's sign = palpation of LIF causes pain in RIF (parietal irritation).
Q16
The sympathetic trunk (paravertebral chain) is formed by paravertebral ganglia. The correct total number of ganglia is:
TMU Slide 15
A. 3 cervical + 12 thoracic + 5 lumbar + 5 sacral + 1 coccygeal = 26 pairs
B. 3 cervical + 12 thoracic + 5 lumbar + 2 sacral + 2 coccygeal = 24 pairs
C. 4 cervical + 12 thoracic + 4 lumbar + 4 sacral + 1 coccygeal = 25 pairs
D. 3 cervical + 10–12 thoracic + 4–5 lumbar + 2–3 sacral + 1 coccygeal ≈ 22 ganglia each side
✓ Answer: D — 3 cervical + 10–12 thoracic + 4–5 lumbar + 2–3 sacral + 1 coccygeal
The sympathetic chain has variable numbers. Per the TMU slides: cervical = 3 pairs (superior, middle, inferior cervical ganglia); thoracic = 10–12 pairs; lumbar = 4–5 pairs; sacral = 2–3 pairs; coccygeal = one unpaired ganglion impar. Total approximately 22 ganglia each side. The inferior cervical ganglion often fuses with T1 to form the stellate (cervicothoracic) ganglion.
⚠ The classic simplified teaching is 3-12-4-4-1 = ~24. Slide says 3 cervical, 10–12 thoracic, 4–5 lumbar, 2–3 sacral. Exact numbers vary slightly by source — learn the format not a single total. The stellate ganglion (T1 + inferior cervical) is the surgical target for upper limb hyperhidrosis.
Q17
Horner's syndrome results from interruption of the sympathetic pathway to the face. Which combination of signs is correct?
Gray's 4e; TMU Review Slide
A. Ptosis + miosis (constricted pupil) + anhydrosis + enophthalmos
B. Ptosis (drooping upper lid) + mydriasis (dilated pupil) + hyperhidrosis
C. Exophthalmos + miosis + hyperhidrosis
D. Ptosis + mydriasis + anhydrosis
✓ Answer: A — Ptosis + miosis + anhydrosis + enophthalmos
Horner's syndrome = loss of cervical sympathetic supply. Four classic signs: (1) Ptosis (partial) — loss of superior tarsal muscle (Müller's muscle) which assists levator palpebrae; (2) Miosis — loss of dilator pupillae (sympathetic), leaving parasympathetic sphincter unopposed; (3) Anhydrosis — loss of sympathetic (cholinergic) supply to facial sweat glands; (4) Enophthalmos — apparent sinking of eyeball (loss of inferior tarsal muscle tone). Causes: Pancoast tumour, carotid dissection, cervical cord lesion.
⚠ A = mydriasis is the OPPOSITE (sympathetic activates dilator pupillae; its loss = miosis). D = mydriasis + anhydrosis is contradictory. Enophthalmos in Horner's is often “apparent” (pseudo-enophthalmos from ptosis). Mnemonic: PAMELA — Ptosis, Anhydrosis, Miosis, Enophthalmos, Loss of ciliospinal reflex, Apparent.
Q18
White rami communicantes are present only at T1–L2 levels because they contain:
TMU Slide 18
A. Postganglionic unmyelinated sympathetic fibres leaving the chain
B. Preganglionic myelinated sympathetic fibres entering the chain
C. Postganglionic myelinated parasympathetic fibres
D. Sensory fibres from visceral afferents
✓ Answer: B — Preganglionic myelinated sympathetic fibres entering the chain
White rami communicantes carry preganglionic sympathetic fibres (myelinated → appear white) from the spinal nerve to the sympathetic chain ganglion. They exist only at T1–L2 because those are the only segments with preganglionic sympathetic cell bodies in the lateral grey horn. The fibres are myelinated; the “white” appearance distinguishes them from grey rami. They also carry visceral afferent (sensory) fibres back.
⚠ A = describes GREY rami communicantes (postganglionic, unmyelinated, leave chain at ALL levels C1–Co). White = myelinated, preganglionic, T1–L2 only. Grey = unmyelinated, postganglionic, all spinal levels. Both carry some visceral afferents as well.
Q19
Grey rami communicantes differ from white rami communicantes in that grey rami:
TMU Slide 18
A. Are present only at T1–L2 and carry myelinated fibres
B. Carry preganglionic fibres into the sympathetic chain
C. Are present at all spinal levels and carry postganglionic unmyelinated fibres back to spinal nerves
D. Carry parasympathetic fibres to thoracic viscera
✓ Answer: C — All levels, postganglionic unmyelinated fibres to spinal nerves
Grey rami communicantes carry postganglionic sympathetic fibres (unmyelinated → appear grey) from the sympathetic chain ganglion back to the spinal nerve, whence they travel to the periphery to supply blood vessels, sweat glands, and arrector pili muscles of the skin. They are present at all 31 spinal levels (because all spinal nerves need sympathetic supply to their peripheral distributions), even at cervical and sacrococcygeal levels where there are no white rami.
⚠ Key distinction: White rami = preganglionic, myelinated, only T1–L2 (where sympathetic cells are). Grey rami = postganglionic, unmyelinated, ALL spinal levels. The cervical sympathetic ganglia (superior, middle, inferior) receive white rami indirectly (fibres ascend in the chain from T1) but send grey rami to all cervical spinal nerves.
Q20
Which autonomic feature is correctly stated?
TMU Slides 21, 30, 33
A. Sympathetic: decreases heart rate; parasympathetic: increases heart rate
B. Sympathetic: dilates bronchi + increases heart rate; parasympathetic: constricts bronchi + decreases heart rate
C. Sympathetic: constricts pupils; parasympathetic: dilates pupils
D. Sympathetic: increases GI motility; parasympathetic: decreases GI motility
✓ Answer: B — Sympathetic dilates bronchi + increases HR; Parasympathetic constricts bronchi + decreases HR
Fight-or-flight (sympathetic): tachycardia, bronchodilation, vasoconstriction of skin/GI, vasodilation of skeletal muscle, pupil dilation, GI motility decrease, glycogenolysis, piloerection, sweating. Rest-and-digest (parasympathetic): bradycardia, bronchoconstriction, GI motility increase (the “D activities” — digestion, defaecation, diuresis), pupil constriction, lacrimation, salivation.
⚠ A = reversed. C = reversed (sympathetic = pupil dilation via dilator pupillae; parasympathetic = constriction via sphincter pupillae). D = reversed (sympathetic inhibits GI; parasympathetic promotes GI). B is the only correct pairing.
D1 Splanchnic Nerves +
Splanchnic nerves are bundles of preganglionic sympathetic fibres that leave the sympathetic chain to synapse in prevertebral (collateral) ganglia rather than within the paravertebral chain itself. Three thoracic splanchnic nerves: (1) Greater splanchnic (T5–T9) → coeliac ganglion → foregut + adrenal medulla; (2) Lesser splanchnic (T10–T11) → superior mesenteric ganglion → midgut; (3) Least (lowest) splanchnic (T12) → renal plexus/aorticorenal ganglion → kidney + ureter. Lumbar splanchnics (L1–L2) relay at the inferior mesenteric ganglion (hindgut). Sacral splanchnics carry sympathetics to pelvic organs. The word “splanchnic” (from Greek splanchnon = viscus) refers to any nerve serving the viscera.
TMU Slide 17 · Gray's Anatomy 4e
D2 Referred Pain +
Referred pain is the perception of pain at a body surface site remote from the actual diseased/injured organ. Mechanism (convergence theory): visceral afferent fibres from an organ and somatic afferent fibres from a corresponding dermatome converge on the same second-order neurons in the dorsal horn of the spinal cord. The brain “misinterprets” the visceral signal as originating from the familiar dermatome. Characteristics: poorly localised, dull, may be associated with hyperalgesia of the skin surface. Clinical examples: cardiac ischaemia → left arm + jaw (T1–T5); appendicitis → periumbilical then RIF (T10 → L1); diaphragmatic irritation → shoulder tip (C3–C5 phrenic); renal colic → loin to groin (T10–L1).
TMU Slides 38–39 · Gray's Anatomy 4e
D3 Horner's Syndrome +
Horner's syndrome is the clinical triad (classically tetrad) resulting from interruption of the cervical sympathetic pathway at any point along its three-neuron arc (hypothalamus → ciliospinal centre C8–T2 → superior cervical ganglion → eye). Signs: (1) Ptosis — partial drooping of upper lid (Müller's muscle paralysis); (2) Miosis — small pupil (dilator pupillae paralysis, sphincter unopposed); (3) Anhydrosis — loss of ipsilateral facial sweating (sympathetic cholinergic supply lost); (4) Enophthalmos — apparent sinking of the globe (loss of inferior tarsal muscle). Causes by level: central (stroke, MS), pre-ganglionic (Pancoast lung apex tumour, thyroid carcinoma, cervical rib, carotid artery dissection), post-ganglionic (carotid/cavernous sinus disease).
Gray's Anatomy 4e · TMU Slide 33
D4 The Four Cranial Parasympathetic Ganglia +
Four ganglia mediate the cranial (parasympathetic) outflow. All are located in the head and all postganglionic fibres “hitch-hike” on branches of the trigeminal nerve (CN V) to reach their targets:

(1) Ciliary ganglion — CN III → sphincter pupillae (miosis) + ciliary muscle (accommodation). Located in orbit.
(2) Pterygopalatine (sphenopalatine) ganglion — CN VII (greater petrosal nerve) → lacrimal gland + nasal + palatine mucous glands. Located in pterygopalatine fossa. Fibres travel with CN V2 (maxillary nerve) branches.
(3) Submandibular ganglion — CN VII (chorda tympani → lingual nerve) → sublingual gland + submandibular gland. Located on the hyoglossus muscle.
(4) Otic ganglion — CN IX (lesser petrosal nerve) → parotid gland. Located below foramen ovale; fibres travel with auriculotemporal nerve (CN V3).
TMU Slide 25 · Gray's Anatomy 4e
D5 Rami Communicantes (White and Grey) +
Rami communicantes are connecting branches between each spinal nerve and the sympathetic chain ganglion at the same level. Two types:

White rami communicantes: carry preganglionic sympathetic fibres (myelinated → appear white/glistening) from the spinal nerve into the sympathetic chain. Present only at T1–L2 (levels where sympathetic preganglionic cell bodies lie in the lateral grey horn). They also carry visceral afferents (pain fibres) returning from viscera.

Grey rami communicantes: carry postganglionic sympathetic fibres (unmyelinated → appear grey/dull) from the sympathetic chain ganglion back to the spinal nerve for distribution to blood vessels, sweat glands, and arrector pili of the skin. Present at all 31 spinal levels (every spinal nerve needs sympathetic skin supply). Grey rami from the cervical ganglia supply the cervical spinal nerves even though no white rami enter there directly (fibres ascend in the chain from T1).
TMU Slide 18 · Gray's Anatomy 4e
D6 Prevertebral vs Paravertebral Ganglia +
Paravertebral (sympathetic chain) ganglia: situated on either side of the vertebral column forming the sympathetic trunk. Number: ~22 per side (3 cervical + 10–12 thoracic + 4–5 lumbar + 2–3 sacral + 1 coccygeal ganglion impar). Receive white rami (preganglionic) and send grey rami (postganglionic) to all spinal nerves. Postganglionic fibres supply skin, blood vessels, sweat glands, and arrector pili.

Prevertebral (collateral/preaortic) ganglia: unpaired ganglia located in front of the vertebral column, around the abdominal aorta. Names: coeliac ganglion, superior mesenteric ganglion, inferior mesenteric ganglion, aorticorenal ganglion. They receive preganglionic fibres from the splanchnic nerves and send postganglionic fibres along blood vessel branches to supply abdominal and pelvic viscera. They do NOT communicate with spinal nerves directly.

Key distinction: paravertebral = close to spine, supply somatic structures of body wall + head/neck viscera; prevertebral = in abdomen/pelvis, supply abdominal/pelvic viscera via splanchnic routes.
TMU Slides 14–17 · Gray's Anatomy 4e
Essay 1
Describe the sympathetic nervous system: its origin (lower centre), the paravertebral chain, the four patterns of distribution from the chain, and the main effects of sympathetic stimulation.
10 marks

Origin — Lower Centre

Preganglionic sympathetic cell bodies lie in the lateral grey horn of spinal cord segments T1 to L2 (thoracolumbar outflow). Preganglionic fibres exit via the anterior root, join the spinal nerve, and reach the sympathetic chain via white rami communicantes (myelinated, T1–L2 only).

Paravertebral Chain (Sympathetic Trunk)

  • Two chains of ganglia lying on either side of the vertebral column, from base of skull to coccyx
  • Ganglia connected by interganglionic branches forming the trunk
  • Numbers: 3 cervical + 10–12 thoracic + 4–5 lumbar + 2–3 sacral + 1 coccygeal (ganglion impar)
  • Inferior cervical ganglion + T1 often fuse = stellate (cervicothoracic) ganglion

Four Patterns of Distribution from the Chain

  • Pattern 1 — Synapse in chain, return via grey rami communicantes: Postganglionic fibres re-enter spinal nerve via grey ramus (unmyelinated, all levels) → distributed to blood vessels, sweat glands, arrector pili of the body wall and limbs
  • Pattern 2 — Synapse in chain, leave via named nerve branches: Postganglionic fibres pass directly from the chain as named branches (e.g. cervical cardiac branches, pulmonary branches) to reach heart, lungs, oesophagus, trachea
  • Pattern 3 — Pass through chain without synapsing → synapse in prevertebral ganglion: Preganglionic fibres form splanchnic nerves (greater T5–9, lesser T10–11, least T12) → synapse in coeliac, SMA, or renal ganglia → postganglionic fibres travel along blood vessels to supply abdominal viscera
  • Pattern 4 — Adrenal medulla: Preganglionic fibres pass directly (via greater splanchnic) to the adrenal medulla (modified postganglionic) → release adrenaline + noradrenaline into bloodstream

Main Effects of Sympathetic Stimulation (“Fight or Flight”)

  • Heart: increased rate + force (tachycardia); coronary dilation
  • Lungs: bronchodilation (β2 receptors)
  • Blood vessels: skin + splanchnic vasoconstriction (α); skeletal muscle vasodilation (β2)
  • Eyes: pupil dilation (dilator pupillae, α1); upper eyelid retraction (superior tarsal)
  • GI: decreased motility + sphincter contraction
  • Skin: sweating (cholinergic exception); piloerection
  • Adrenal medulla: adrenaline + noradrenaline secretion
  • Liver: glycogenolysis → raised blood glucose
Marking (10 marks): Origin / lateral grey horn / T1–L2 (1) · White rami and chain structure (1) · Correct ganglion numbers per region (1) · Four patterns of distribution, each clearly named (4) · At least four correct sympathetic effects (2) · Adrenal medulla mentioned as special case (1)
Essay 2
Describe the parasympathetic nervous system: the craniosacral outflow, the four cranial ganglia and what each supplies, and the sacral (pelvic splanchnic) outflow and its targets.
10 marks

Overview — Craniosacral Outflow

The parasympathetic division is the craniosacral outflow. Preganglionic neurons are in cranial nerve nuclei (brainstem) and sacral cord S2–S4. Preganglionic fibres are long and myelinated; postganglionic fibres are short and unmyelinated. Both release acetylcholine. Ganglia are located close to or within the wall of the target organ.

Cranial Component — Four Cranial Ganglia

  • Ciliary ganglion (CN III): Preganglionic fibres from Edinger-Westphal nucleus via CN III → ciliary ganglion in orbit → short ciliary nerves → sphincter pupillae (miosis) + ciliary muscle (accommodation)
  • Pterygopalatine ganglion (CN VII): Preganglionic via greater petrosal nerve (branch of CN VII) → pterygopalatine ganglion in pterygopalatine fossa → via CN V2 branches → lacrimal gland + nasal mucosa + palatine glands (secretomotor)
  • Submandibular ganglion (CN VII): Preganglionic via chorda tympani → lingual nerve (CN V3) → submandibular ganglion on hyoglossus → submandibular gland + sublingual gland (secretomotor)
  • Otic ganglion (CN IX): Preganglionic via tympanic nerve → tympanic plexus → lesser petrosal nerve → otic ganglion (below foramen ovale) → auriculotemporal nerve (CN V3) → parotid gland (secretomotor)

Vagus Nerve (CN X) — No Named Peripheral Ganglion

CN X is the dominant cranial parasympathetic nerve. It supplies the thoracic viscera (heart, lungs) and abdominal viscera to the left colic (splenic) flexure. Ganglion cells are located in the walls of the target organs (intramural ganglia). Effects: bradycardia, bronchoconstriction, increased GI motility.

Sacral Component — Pelvic Splanchnic Nerves (S2–S4)

  • Preganglionic fibres arise from sacral parasympathetic nucleus in lateral grey horn of S2–S4
  • Exit as pelvic splanchnic nerves (nervi erigentes)
  • Targets: descending + sigmoid colon, rectum; urinary bladder (detrusor muscle → micturition); erectile tissue (penis/clitoris → erection via NO-mediated vasodilation); uterus
  • Ganglion cells are in the pelvic plexus and in organ walls
Marking (10 marks): Craniosacral outflow statement (1) · Each of the four ganglia with correct CN + target (4 × 1 = 4) · Vagus supply to splenic flexure + cardiac/pulmonary (1) · Pelvic splanchnic origin S2–S4 (1) · Pelvic targets: colon/bladder/genitalia (2) · Pre/postganglionic fibre characteristics (1)
Essay 3
Describe the autonomic control of the eye: the pupillary light reflex pathway (CN II → CN III), the sympathetic pathway, the accommodation reflex, and the clinical features of Horner's syndrome.
10 marks

Pupillary Light Reflex (Parasympathetic, Constriction)

  • Afferent limb (CN II): Light detected by retinal photoreceptors → ganglion cells → optic nerve → optic chiasm → optic tract → pretectal nucleus of midbrain (NOT lateral geniculate nucleus — this bypasses the visual cortex)
  • Efferent limb (CN III — bilateral): Pretectal nucleus → bilateral Edinger-Westphal nuclei (CN III parasympathetic nucleus) → preganglionic fibres travel in CN III → ciliary ganglion (in orbit) → short ciliary nerves → sphincter pupillae → miosis
  • Bilateral projection explains the consensual reflex: light in one eye constricts both pupils

Accommodation Reflex (Near Vision)

  • Visual cortex perceives blurred near image → signals to pretectal area → Edinger-Westphal nucleus
  • CN III → ciliary ganglion → ciliary muscle contracts → zonule (suspensory ligament) relaxes → lens rounds up (increases convexity) → focus for near objects
  • Simultaneously: medial rectus muscles contract (convergence) + sphincter pupillae contract (miosis) = near reflex triad

Sympathetic Pathway to the Eye

  • First neuron: Hypothalamus → ipsilateral ciliospinal centre (C8–T2) in lateral grey horn
  • Second neuron: Preganglionic → white ramus → T1 sympathetic chain → ascends to superior cervical ganglion (at C2–C3) → synapses
  • Third neuron: Postganglionic fibres travel along internal carotid artery → through cavernous sinus → via nasociliary nerve branch (CN V1) → long ciliary nerves → dilator pupillae (mydriasis) + superior tarsal (Müller's) muscle (lid retraction) + inferior tarsal muscle

Horner's Syndrome

Interruption anywhere along the three-neuron sympathetic arc to the eye produces:

  • Ptosis (partial) — loss of superior tarsal muscle
  • Miosis — dilator pupillae paralysed; sphincter unopposed
  • Anhydrosis (ipsilateral face) — loss of sympathetic (cholinergic) sweat gland supply
  • Enophthalmos (apparent) — loss of inferior tarsal muscle tone
  • Causes by level: Central = stroke, MS, syringomyelia; Pre-ganglionic = Pancoast tumour (T1 root), cervical rib, carotid dissection, thyroid carcinoma; Post-ganglionic = carotid/cavernous sinus pathology
Marking (10 marks): Afferent limb CN II → pretectal nucleus (1) · Efferent limb CN III → ciliary ganglion → sphincter pupillae (2) · Consensual reflex explanation (1) · Accommodation triad: convergence + ciliary + miosis (1) · Three-neuron sympathetic arc to eye (2) · All four Horner's signs (2) · One clinical cause per level (1)
Essay 4
Describe the three thoracic splanchnic nerves: their segmental origin, course, ganglion of relay, and targets. Include the adrenal medulla's special relationship to the splanchnic innervation.
8 marks

Greater Splanchnic Nerve

  • Origin: Preganglionic sympathetic fibres from T5–T9 (pass through chain without synapsing)
  • Course: Descends obliquely over vertebral bodies → passes through the crus of the diaphragm
  • Relay: Coeliac ganglion (largest prevertebral ganglion, at level T12/L1 around coeliac artery)
  • Targets: Foregut (stomach, liver, gallbladder, spleen, pancreas, upper duodenum) via coeliac plexus branches
  • Adrenal medulla: Some preganglionic fibres from the greater splanchnic nerve bypass the coeliac ganglion and terminate directly on chromaffin cells of the adrenal medulla (modified postganglionic neurons → adrenaline + noradrenaline release)

Lesser Splanchnic Nerve

  • Origin: T10–T11
  • Course: Passes through diaphragm (or crus)
  • Relay: Superior mesenteric ganglion (around SMA origin at L1)
  • Targets: Midgut (lower duodenum, jejunum, ileum, ascending + transverse colon to splenic flexure)

Least (Lowest) Splanchnic Nerve

  • Origin: T12 (when present; variable)
  • Relay: Renal plexus / aorticorenal ganglion
  • Targets: Kidney, proximal ureter

Adrenal Medulla — Special Case

The adrenal medulla is embryologically derived from neural crest cells and is functionally a modified sympathetic ganglion. It is innervated directly by preganglionic sympathetic fibres (mainly from the greater splanchnic nerve), bypassing any postganglionic relay. The chromaffin cells = modified postganglionic neurons. On stimulation they secrete adrenaline (80%) + noradrenaline (20%) into the bloodstream, providing a widespread, amplified sympathetic response during “fight-or-flight.”

Marking (8 marks): Greater splanchnic: origin T5–9 + coeliac ganglion + foregut targets (2) · Lesser splanchnic: origin T10–11 + SMA ganglion + midgut (2) · Least splanchnic: T12 + renal plexus (1) · Adrenal medulla: direct preganglionic innervation + modified postganglionic + adrenaline/noradrenaline (2) · All fibres pierce diaphragm stated (1)
Essay 5
Explain the mechanism of referred pain. Describe the pathway and dermatomes for cardiac pain, and the two-phase pain migration in acute appendicitis. Add two further clinical examples.
8 marks

Mechanism of Referred Pain

Referred pain arises from the convergence of visceral and somatic afferent fibres on the same second-order neurons in the dorsal horn of the spinal cord. The brain cannot distinguish which source activated that neuron and defaults to the more familiar somatic interpretation → pain is “felt” in the dermatome supplied by those spinal segments rather than at the diseased organ. Visceral pain is dull, diffuse, poorly localised, and often midline; once parietal peritoneum or adjacent somatic structures are irritated, pain becomes sharp and well-localised.

Cardiac Pain (Angina / MI)

  • Cardiac afferents travel with sympathetic fibres via the cardiac plexus → enter spinal cord at T1–T5
  • These levels also receive somatic afferents from the medial left arm (T1–T2) + precordium (T2–T5) + jaw (upper cardiac via C3/C4 referral)
  • Pain is referred to: left arm + shoulder + jaw + precordium
  • Clinical: silent MI occurs in diabetic autonomic neuropathy (afferent fibres damaged); right coronary territory can refer to right arm

Appendicitis — Two-Phase Pain Migration

  • Phase 1 (visceral, early): Appendiceal inflammation activates visceral afferents → travel via mesenteric plexus → enter spinal cord at T10 → referred to periumbilical region (T10 dermatome = level of umbilicus). Pain is dull, poorly localised, central/periumbilical. Nausea is common (same spinal level).
  • Phase 2 (somatic, late): Inflammation spreads to parietal peritoneum overlying the appendix → somatic afferents (ilioinguinal + iliohypogastric, L1) activated → pain is sharp, well-localised to McBurney's point (RIF). Guarding, rebound tenderness, and Rovsing's sign appear.

Two Further Clinical Examples

  • Diaphragmatic irritation (e.g. sub-phrenic abscess, ruptured spleen → haemoperitoneum): phrenic nerve afferents (C3–C5) → referred pain to ipsilateral shoulder tip (Kehr's sign). Supraclavicular fossa dermatome = C3–C4 → same segments as phrenic.
  • Renal/ureteric colic: ureteric smooth muscle spasm activates T10–L1 afferents → referred pain from loin to groin (T10–L1 dermatomes), often radiating to the ipsilateral testis/labium majus. Haematuria distinguishes from appendicitis; pain is typically colicky.
Marking (8 marks): Convergence theory correctly explained (2) · Cardiac: T1–T5 + left arm + jaw correctly linked (2) · Appendix phase 1 (T10 periumbilical visceral) + phase 2 (somatic RIF) (2) · Two additional examples with correct spinal levels (2)