Accessory Structures: These include the eyelids, eyelashes, eyebrows, lacrimal apparatus, and extrinsic eye muscles. They provide protection, lubrication, and movement for the eye.
Cornea: The transparent outer layer of the eye that helps focus light as it enters.
Lens: A flexible structure that focuses light onto the retina. Its shape is adjusted by ciliary muscles to allow for near and far vision.
Humors: The eye contains fluids called humors.
Aqueous humor: Fills the anterior cavity between the cornea and the lens.
Vitreous humor: Fills the posterior cavity between the lens and the retina, maintaining eye shape and supporting the retina.
Fibrous Layer: The outermost layer.
Sclera: Provides protection and shape.
Cornea: Focuses light.
Vascular Layer (Uvea): The middle layer.
Choroid: Contains blood vessels and pigment to absorb scattered light.
Ciliary Body: Controls lens shape, produces aqueous humor.
Iris: Controls pupil size, regulating light entry.
Inner Layer:
Retina: Contains photoreceptors (rods and cones) that transduce light into neural signals.
Light passes through the cornea, aqueous humor, pupil, lens, and vitreous humor before reaching the retina.
Refraction: The bending of light rays occurs primarily at the cornea and lens.
The lens changes shape (accommodation) to focus light from objects at different distances.
Phototransduction: Light striking the retina activates photoreceptors (rods and cones).
Photoreceptors hyperpolarize in response to light, reducing the release of inhibitory neurotransmitters.
This triggers a cascade of events in bipolar cells and ganglion cells, leading to action potentials in ganglion cells.
Axons of ganglion cells converge to form the optic nerve, transmitting signals to the brain.
The optic disc is the area where the optic nerve exits the eye; it contains no photoreceptors, creating a blind spot.
We don’t typically notice the blind spot because:
Each eye compensates for the other's blind spot.
The brain fills in the missing information.
Rods:
More sensitive to light; function in dim light.
Provide black and white vision.
Concentrated in the periphery of the retina.
Cones:
Require brighter light; function in daylight.
Provide color vision.
Concentrated in the fovea (center of the retina).
The image is inverted and reversed on the retina due to refraction.
The brain corrects the image orientation during visual processing.
Outer Ear: Collects sound waves.
Pinna (auricle): Directs sound into the auditory canal.
Auditory Canal: Transmits sound to the tympanic membrane.
Middle Ear: Amplifies sound waves.
Tympanic Membrane (eardrum): Vibrates in response to sound.
Ossicles (malleus, incus, stapes): Transmit and amplify vibrations to the oval window.
Inner Ear: Converts sound waves into neural signals and maintains balance.
Cochlea: Contains receptors for hearing.
Vestibular Apparatus: Contains receptors for balance.
Loudness: Determined by the amplitude of the sound wave.
Pitch: Determined by the frequency of the sound wave.
Location: Determined by the timing and intensity differences between the two ears.
Sound waves cause the tympanic membrane to vibrate, which moves the ossicles.
The stapes transmits vibrations to the oval window, causing pressure waves in the perilymph of the cochlea.
These pressure waves cause the basilar membrane to vibrate.
Hair cells on the basilar membrane are deflected, opening mechanically gated ion channels.
Ion influx depolarizes the hair cells, causing them to release neurotransmitters and stimulate auditory nerve fibers.
Semicircular Canals: Detect rotational movements.
Otolith Organs (utricle and saccule): Detect linear acceleration and head position.
Hair cells in these organs are deflected by movement, similar to those in the cochlea.
Vestibular information is integrated in the vestibular nuclei of the brainstem.
Outputs project to:
Cerebellum: Coordination of movement.
Motor nuclei: Reflexive eye movements and postural adjustments.
Thalamus: Conscious awareness of spatial orientation and movement
Conductive Deafness: Impaired sound transmission through the outer or middle ear (e.g., otitis media).
Sensorineural Deafness: Damage to the inner ear or auditory nerve.
Otitis Media: Middle ear infection.
Tinnitus: Ringing in the ears.
Meniere’s Syndrome: Inner ear disorder causing vertigo, tinnitus, and hearing loss.
Taste (gustation): Detection of chemicals dissolved in saliva.
Smell (olfaction): Detection of airborne chemicals.
Taste and smell receptors transduce chemical signals into neural signals, which are interpreted by the brain.
Endocrine System:
Releases hormones into the bloodstream.
Slower, longer-lasting effects.
Widespread effects on multiple target organs.
Exocrine Glands:
Secrete products into ducts that lead to specific locations (e.g., sweat glands, salivary glands).
Nervous System:
Uses electrical signals (action potentials) and neurotransmitters.
Fast, short-lived effects.
Localized effects.
Hyperfunction: Excessive hormone production.
Hypofunction: Insufficient hormone production.
Altered Tissue Responsiveness: Target tissues do not respond properly to hormones.
Primary Disorders: Problem with the gland itself.
Secondary Disorders: Problem with the pituitary gland.
Tertiary Disorders: Problem with the hypothalamus.
Diagnosis: Hormone level measurements, stimulation/suppression tests, imaging.
Humoral Stimulation: Hormone release caused by altered levels of certain critical ions or nutrients (e.g., Ca2+$$Ca^{2+}$$).
Neural Stimulation: Hormone release caused by neural input (e.g., adrenal medulla).
Hormonal Stimulation: Hormone release caused by another hormone (e.g., tropic hormones from the pituitary).
Rate of Synthesis and Release: How much hormone is being produced.
Rate of Degradation and Elimination: How quickly the hormone is broken down or removed from the body.
Negative Feedback: Rising hormone levels inhibit further hormone release.
Amino Acid Derivatives:
Examples: epinephrine, norepinephrine, thyroid hormones.
Can be water-soluble or lipid-soluble.
Peptide Hormones:
Examples: insulin, growth hormone.
Water-soluble.
Bind to receptors on the cell surface.
Steroid Hormones:
Examples: cortisol, testosterone, estrogen.
Lipid-soluble.
Synthesized from cholesterol.
Bind to intracellular receptors.
Water-Soluble Hormones:
Bind to receptors on the cell membrane.
Activate intracellular signaling pathways (e.g., second messengers like cAMP).
Rapid effects.
Lipid-Soluble Hormones:
Diffuse through the cell membrane.
Bind to intracellular receptors in the cytoplasm or nucleus.
Alter gene transcription.
Slower, longer-lasting effects.
Connected to the hypothalamus via the infundibulum.
Posterior Pituitary: Stores and releases hormones produced by the hypothalamus (ADH and oxytocin).
Anterior Pituitary: Produces and releases its own hormones, regulated by hypothalamic hormones.
Feedback Loops: Hormones from target glands feed back to the pituitary and hypothalamus.
Antidiuretic Hormone (ADH): Promotes water retention by the kidneys.
Oxytocin: Stimulates uterine contractions during childbirth and milk ejection.
Growth Hormone (GH): Promotes growth and metabolism.
Thyroid-Stimulating Hormone (TSH): Stimulates thyroid hormone release.
Adrenocorticotropic Hormone (ACTH): Stimulates adrenal cortex hormone release.
Follicle-Stimulating Hormone (FSH): Stimulates follicle development and sperm production.
Luteinizing Hormone (LH): Stimulates ovulation and testosterone production.
Prolactin (PRL): Stimulates milk production.
Located in the neck.
Thyroid Hormone (T3 and T4): Regulates metabolism, growth, and development.
Calcitonin: Lowers blood calcium levels.
Growth Hormone:
Gigantism/Acromegaly: Excessive GH.
Dwarfism: Insufficient GH.
Thyroid Hormone:
Hyperthyroidism: Excessive TH (e.g., Graves' disease).
Hypothyroidism: Insufficient TH (e.g., Hashimoto's thyroiditis).
Adrenal Medulla Dysfunction:
Pheochromocytoma: Tumor of the adrenal medulla, causing excessive catecholamine release.
Located on top of the kidneys.
Adrenal Medulla: Secretes epinephrine and norepinephrine (catecholamines).
Adrenal Cortex: Secretes corticosteroids (mineralocorticoids, glucocorticoids, and androgens).
Pancreas: Endocrine and exocrine functions.
Insulin: Decreases blood glucose levels by promoting glucose uptake by cells.
Glucagon: Increases blood glucose levels by stimulating glycogen breakdown in the liver.
Type I Diabetes: Autoimmune destruction of pancreatic beta cells, resulting in insulin deficiency.
Type II Diabetes: Insulin resistance and impaired insulin secretion.
Ovaries (females): Produce estrogen and progesterone.
Testes (males): Produce testosterone.
Hormone Functions: Sexual development, reproductive function, and secondary sex characteristics.
Parathyroid Gland: secretes parathyroid hormone (PTH), which increases blood Ca2+$$Ca^{2+}$$ levels.
PTH (Parathyroid Hormone):
Increases Ca2+$$Ca^{2+}$$ reabsorption in the kidneys.
Stimulates osteoclast activity to release Ca2+$$Ca^{2+}$$ from bone.
Increases Ca2+$$Ca^{2+}$$ absorption in the intestine (indirectly via vitamin D activation).
Disorders:
Hyperparathyroidism: Elevated Ca2+$$Ca^{2+}$$ levels.
Hypoparathyroidism: Low Ca2+$$Ca^{2+}$$ levels.
Hormonal Role: secretes thymosin and thymopoietin, which promote T-cell development.
Immune Role: Site of T-cell maturation.
Alarm Phase: Initial response; epinephrine release (fight or flight).
Resistance Phase: Long-term response; cortisol release.
Exhaustion Phase: Prolonged stress; depletion of resources leading to organ system failure.
Short-Term Stress: Increased heart rate, blood pressure, and energy mobilization.
Long-Term Stress: Immune suppression, increased blood glucose levels, and sodium and water retention.
Endocrine Signaling: Hormones travel through the bloodstream to distant target cells.
Paracrine Signaling: Chemicals act on nearby cells (e.g., eicosanoids).
Eicosanoids:
Locally acting signaling molecules derived from fatty acids.
Examples: prostaglandins, leukotrienes.
Study Guide Final