Study Notes on the Pupil and Related Physiology
Introduction to the Pupil
The pupil is the black circle in the center of the colored iris of the eye.
Function: Allows light to enter the eye, which then passes through the lens to the retina at the back of the eye.
The retina is responsible for picking up light signals and transmitting them to the brain.
Regulation of Pupil Size
The size of the pupil is adjustable, allowing the body to control light entry.
Meiosis: The contraction or shrinking of the pupil.
Mydriasis: The dilation or increase in size of the pupil.
Regulation: Changes in pupil size are controlled autonomously and cannot be voluntarily manipulated.
Anatomy of the Iris
Iris: The colored portion surrounding the pupil, composed primarily of smooth muscle.
Muscle Groups:
Sphincter Pupillae:
Nature: Circular muscle.
Function: Contracts to decrease pupil size (meiosis).
Dilator Pupillae:
Nature: Radially oriented muscle with fibers extending from the center.
Function: Contracts to increase pupil size (mydriasis).
Neural Pathways of Meiosis (Pupillary Contraction)
Controlled by the Parasympathetic Nervous System.
Involves a two-neuron pathway:
First Neuron: Begins at the Edinger Westphal nucleus in the midbrain (near cranial nerve III or oculomotor nucleus).
Second Neuron: Travels to the ciliary ganglion, located behind the eye, where it synapses.
Transmission: Ciliary ganglion neurons signal the sphincter pupillae muscle via short ciliary nerves.
Neurotransmitter: Acetylcholine acts on muscarinic receptors.
Clinical Application: Rule of the Pupil
Important for evaluating cranial nerve III lesions.
Symptoms in lesions of cranial nerve III:
Affected eye appears down and out.
Assess pupil for dilation:
Dilated Pupil: Indicates impacted parasympathetic nerves, often compressed by a mass (e.g., posterior communicating artery aneurysm).
No Dilation: Suggests ischemic damage—often seen in diabetes.
Neural Pathways of Mydriasis (Pupillary Dilation)
Controlled by the Sympathetic Nervous System.
Activation involves the dilator pupillae muscle and inhibition of the sphincter pupillae.
Neurotransmitter: Norepinephrine acts on alpha-1 receptors.
Involves a three-neuron chain:
First Neuron: Originates in the posterior hypothalamus, travels through the brainstem to the spinal cord (ends in ciliospinal center of Budge at C8 to T2).
Second Neuron: Travels from the spinal cord to the superior cervical ganglion, exits at T1, and crosses lung's apical pleura.
Third Neuron: Travels from the superior cervical ganglion to the dilator pupillae muscle alongside the internal carotid artery, passing through the cavernous sinus.
Clinical Condition: Horner Syndrome
Characterized by:
Meiosis (small pupil) due to loss of sympathetic innervation.
Ptosis: Eyelid droop, due to loss of sympathetic input to superior tarsal muscle.
Anhidrosis: Absence of sweating on one side of the face.
Causes: Apical lung tumor, aortic dissection, carotid dissection, and certain strokes (e.g., PICA stroke).
Diagnosis: Disruption of sympathetic pathways can lead to emerging symptoms seen in Horner syndrome.
Diagnostic Tests for Horner Syndrome
Cocaine Test: Blocks norepinephrine reuptake; causes dilation in normal eyes but no effect in Horner syndrome.
Aproclonidine: Alpha agonist that can dilate the meiotic pupil in Horner syndrome, indicating functional dilator muscle despite lack of sympathetic innervation.
Anisocoria (Pupil Size Difference)
Definition: A condition where pupils are unequal in size.
Relation to conditions:
Horner Syndrome: Small pupil is abnormal.
Cranial Nerve III Palsy: Large pupil is abnormal.
Addy's Pupil: Affected pupil typically larger.
Pupillary Reflexes
Pupillary Light Reflex: Tests both eyes’ response to light:
Shine light in one eye; both should constrict (direct response in illuminated eye, consensual response in the opposite eye).
Signals travel to the pretectal nucleus in midbrain which sends signals to Edinger Westphal nuclei bilaterally.
Activated parasympathetic output results in sphincter pupillae muscle contraction.
Marcus Gunn Pupil
Describes a relative afferent pupillary defect where light in one eye produces less constriction than the other eye.
Diagnosis: Use the swinging flashlight test—reduced constriction on the affected side indicates afferent pathway issues.
Classic cause: Optic neuritis, often associated with multiple sclerosis.
Accommodation Reflex
Definition: Process allowing the eye to focus on near objects, involving changes in lens optical power.
Accompanied by miosis (pupil constriction).
Reflex actions during accommodation:
Convergence of both eyes (medial movement).
Accommodation (lens shape change).
Miosis (pupil constriction).
Clinical Correlation: Argyll Robertson Pupil
Finding associated with neurosyphilis.
Characteristics: Bilateral small pupils that constrict to accommodation but not to light (light-near dissociation).
Clinical Documentation of Pupils
Normal finding is documented as PERRLA:
Pupils Equal, Round, and Reactive to Light and Accommodation.
Indicates a complete examination of pupillary reflexes showing normal function.
Conclusion
Summary of key points regarding pupil physiology, anatomy, neural pathways, clinical implications, and reflex testing.