The ciliary ganglion is a bundle of nerve parasympathetic ganglion located just behind the eye in the posterior orbit. It is 1–2 mm in diameter and in humans contains approximately 2,500 neurons. The ganglion contains postganglionic parasympathetic neurons. These neurons supply the pupillary sphincter muscle, which constricts the pupil, and the ciliary muscle which contracts to make the lens more convex. Both of these muscles are involuntary since they are controlled by the parasympathetic division of the autonomic nervous system.
Detailed view of nerves of lateral orbit showing the ciliary ganglion immediately behind the globe of the eye.
|From||sensory root of ciliary ganglion
sympathetic root of ciliary ganglionparasympathetic root of ciliary ganglion
|To||short ciliary nerves|
|Anatomical terms of neuroanatomy|
The ciliary ganglion contains postganglionic parasympathetic neurons that supply the ciliary muscle and the pupillary sphincter muscle. Because of the much larger size of the ciliary muscle, 95% of the in neurons in the ciliary ganglion innervate it compared to the pupillary sphincter.
Three types of axons enter the ciliary ganglion but only the preganglionic parasympathetic axons synapse there. The entering axons are arranged into three roots which join enter the posterior surface of the ganglion:
- The sensory root branches from the nasociliary nerve and travels through the ganglion forming part of the short ciliary nerves. These sensory axons supply the cornea, ciliary body and iris.
- The sympathetic root originates from the internal carotid plexus with cell bodies in the superior cervical ganglion. The axons pass through the ganglion and enter the eye without synapsing into the short ciliary nerves. The sympathetic root contains the postganglionic sympathetic axons that provide sympathetic supply to the blood vessels of the eye. Sometimes, they also supply the pupillary dilator muscle, however these axons usually travel from the nasociliary nerve to the long ciliary nerves to enter the eye.
- The parasympathetic root branches from the inferior division of the oculomotor nerve and carries the preganglionic parasympathetic axons from the Edinger-Westphal nucleus to the ciliary ganglion. Within the ganglion the axons synapse onto the postganglionic parasympathetic neurons. These neurons project axons through the short ciliary nerves to innervate the ciliary muscle and pupillary sphincter muscle.
Short ciliary nervesEdit
Exiting from the anterior surface of the ciliary ganglion are the short ciliary nerves which contain the sensory, postganglionic sympathetic and postganglionic parasympathetic axons to the eye.
Adie tonic pupilEdit
Diseases of the ciliary ganglion produce a "tonic pupil", which is a pupil that does not react to light (it is “fixed”) and has an abnormally slow and prolonged response to attempted near vision (accommodation).
When a person with an Adie pupil attempts to focus on a nearby object, the pupil (which would normally constrict rapidly) constricts slowly. On close inspection, the constricted pupil is not perfectly round. When the person focuses on a more distant object (say the far side of the room), the pupil (which would normally dilate immediately) remains constricted for several minutes, and then slowly dilates back to the expected size.
Tonic pupils are fairly common – they are seen in roughly 1 out of every 500 people. A person with anisocoria (one pupil bigger than the other) whose pupil does not react to light (does not constrict when exposed to bright light) most likely has Adie syndrome – idiopathic degeneration of the ciliary ganglion.
The strange behavior of tonic pupils was first explained by Irene Loewenfeld in 1979. The ciliary ganglion contain many more nerve fibers directed to the ciliary muscle than nerve fibers directed to the constrictor pupillae – roughly twenty times more. The ciliary muscle is also more massive than the constrictor pupillae, again by a factor of twenty. Based on these observations, Loewenfeld proposed an explanation of the tonic pupil. She noted that pathological destruction of nerve cells in the ciliary ganglion that is found in all cases of Adie pupil. In her own words:
- Let’s say that in a given fresh Adie’s pupil, a random 70% of the cells in the ciliary ganglion stop working; and that, in a couple of months, these neurons re-grow and randomly re-innervate both intraocular sphincters (the ciliary muscle and the iris sphincter). Some parasympathetic light-reaction neurons that were originally destined for the iris sphincter will end up innervating the ciliary muscle. But there will not be enough of them to budge that big muscle, so there will be no detectable accommodation with exposure to light. The other way around, it is a different story. There will be plenty of accommodative neurons re-growing into the iris sphincter, and it won’t take very many of them to make a little muscle like the iris sphincter contract. This means that every time the patient accommodates her gaze to a near object, some of the innervation to the ciliary muscle will spill over into the iris and constrict the pupil.
Loewenfeld’s theory is now generally accepted. It explains the defining features of a tonic pupil:
- (1) The pupil does not react to light. The original light-reaction neurons have been destroyed.
- (2) Tonic constriction with attempted near vision. Aberrant regeneration of nerve fibers intended for the ciliary muscle causes abnormal, tonic contraction of the pupil with accommodation.
- (3) Segmental iris constriction. When carefully examined under magnification, the iris does not constrict uniformly with attempted near vision. Only the re-innervated segments contract, producing a slightly irregular contour to the pupil.
- (4) Denervation supersensitivity. Like any denervated muscle, the iris becomes supersensitive to its normal neurotransmitter (in this case, acetylcholine). Very weak solutions of cholinergic substances such as pilocarpine (that have no effect on the normal iris) cause the denervated iris to constrict.
Tonic pupils are usually due to Adie syndrome, but other diseases can denervate the ciliary ganglion. Peripheral neuropathies (such as diabetic neuropathy) occasionally produce tonic pupils. Herpes zoster virus can attack the ciliary ganglion. Trauma to the orbit can damage the short ciliary nerves. Anything that denervates the ciliary ganglion will produce a tonic pupil due to aberrant nerve regeneration.
Adie syndrome is tonic pupil plus absent deep tendon reflexes. Adie syndrome is a fairly common, benign, idiopathic neuropathy that selectively affects the ciliary ganglion and the spinal cord neurons involved in deep tendon reflex arcs. It usually develops in middle age, although it can occur in children. A variant of Adie syndrome, Ross syndrome, affects sweating as well.
Early in the course of Adie syndrome (when the cells of the ciliary ganglion have been destroyed, but before regeneration has occurred) the pupil will be fixed and dilated. The sphincter pupillae will be paralyzed. There will be no response to accommodation – the ciliary muscle is also paralyzed.
With aberrant nerve regeneration, the pupil will remain fixed, but it will constrict with attempted near vision. The constriction will be abnormal (“tonic”).
Late in the course of Adie syndrome, the pupil becomes small (as all pupils do with old age). It will still be “fixed” (it will not constrict to bright light) and it will continue to show abnormal, tonic constriction with attempted near vision.
In some neurological disorders, the pupil does not react to light, but it does react to accommodation. This is called “light-near dissociation”.
In Adie syndrome, damage involving the ciliary ganglion manifests light-near dissociation and a tonically dilated pupil (usually on the same side).
Other causes of light-near dissociation involve damage to the brainstem, where a tonic pupil is not produced. Brainstem causes of light-near dissociation include Argyll Robertson pupil and Parinaud syndrome.
Irene Loewenfeld is generally credited for being the first physiologist to make this distinction.
Plan of oculomotor nerve.
- Perez, GM; Keyser, RB (September 1986). "Cell body counts in human ciliary ganglia". Investigative Ophthalmology & Visual Science. 27 (9): 1428–31. PMID 3744735.
- Kawasaki, A (December 1999). "Physiology, assessment, and disorders of the pupil". Current Opinion in Ophthalmology. 10 (6): 394–400. doi:10.1097/00055735-199912000-00005. PMID 10662243.
- Thompson, HS; Kardon, RH (June 2006). "Irene E. Loewenfeld, PhD Physiologist of the pupil". Journal of Neuro-Ophthalmology. 26 (2): 139–48. doi:10.1097/01.wno.0000222970.02122.a0. PMID 16845317.
- Thompson, HS (1977). "Adie's syndrome: some new observations". Transactions of the American Ophthalmological Society. 75: 587–626. PMC 1311565. PMID 613531.
- Anatomy figure: 29:03-04 at Human Anatomy Online, SUNY Downstate Medical Center - "A deeper dissection of the right orbit from a superior approach."
- Atlas image: n2a4p2 at the University of Michigan Health System - "Branches of Trigeminal Nerve, Lateral View"
- Cell Centered Database - Ciliary ganglion
- lesson3 at The Anatomy Lesson by Wesley Norman (Georgetown University) (orbit5)
- cranialnerves at The Anatomy Lesson by Wesley Norman (Georgetown University) (III, V)