bio 225 exam 2

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the vertebrate central nervous system consists of:

the brain and spinal cord

<p>the brain and spinal cord</p>
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brain

integrating center

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spinal cord

mediates information flow between brain and body (and vice versa)

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nuclei

groups of neuronal cell bodies within the CNS

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tracts

bundles of many axons within the CNS

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ascending vs descending tracts

  • ascending: carries info up to brain

  • descending: carries info from brain down along spinal cord


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vertebrate peripheral nervous system consists of what?

  • all the neurons outside of the CNS

  • nerves and ganglia


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nerves

  • bundles of many axons outside of the CNS (leaving CNS)

  • consists of myelinated and unmyelinated axons enclosed in connective tissue

  • may contain sensory or motor or both

  • cranial vs spinal - classified based on what CNS they’re coming off of


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ganglia

groups of neuronal cell bodies outside of the CNS

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white matter

  • shiny, bright appearance

  • primarily composed of myelinated axons

  • don’t typically see cell bodies + dendrites


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grey matter

  • dulled appearance

  • contains dendrites, cell bodies, and unmyelinated axons

  • short axons


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organization of white and grey matter in brain vs spinal cord

brain: grey matter surrounds white

spinal cord: white matter surrounds grey in a butterfly design

<p>brain: grey matter surrounds white</p><p>spinal cord: white matter surrounds grey in a butterfly design</p>
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structure and function of spinal cord

  • mediates spinal reflexes

  • pathway for impulses to and from the brain

  • receives afferent/sensory signals via dorsal root

    • somatosensory neuron cell bodies in the dorsal root ganglion

  • sends out efferent/motor signals via ventral root

    • motor neuron cell bodies in the ventral horn


pic: blue is afferent/sensory going in, red is efferent/motor going out

<ul><li><p>mediates spinal reflexes</p></li><li><p>pathway for impulses to and from the brain</p></li><li><p>receives afferent/sensory signals via dorsal root </p><ul><li><p>somatosensory neuron cell bodies in the dorsal root ganglion</p></li></ul></li><li><p>sends out efferent/motor signals via ventral root</p><ul><li><p>motor neuron cell bodies in the ventral horn</p></li></ul></li></ul><p></p><p>pic: blue is afferent/sensory going in, red is efferent/motor going out</p>
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how does the withdrawal reflex achieve a coordinated movement?


It simultaneously activates required motor neurons and inhibits opposing ones to ensure smooth movement.

<p></p><p><span>It simultaneously <strong>activates</strong> required motor neurons and <strong>inhibits</strong> opposing ones to ensure smooth movement.</span></p>
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what are reflex arcs and how does divergence work in them?

  • reflex arc: control many involuntary behaviors, most of which are mediated by multiple neurons and employ divergence

  • divergence: 1 receptor spreads its signal to many effectors


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What is the pathway of a reflex arc, and what is the role of interneurons?

  • pathway: sensory neuron → interneuron → motor neuron

  • interneurons: have short, branching axons that synapse onto multiple targets (motor neurons) to spread signal via divergence


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simple reflex arcs

  • rare

  • contains only a single synapase/location of synapses

  • requires only 2 neurons (cluster of neurons)

  • 1 sensory signal in, 1 motor signal out

  • ex: patellar reflex


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contralateral - def and ascending vs. descending tracts

  • opposite side

  • most signals between the body and the brain (and vice versa) are contralateral

  • ascending tracts carry afferent/sensory signals within the CNS

    • in from lefthand side, crossing over to righthand side of spinal cord, up to the right somatosensory cortex

  • descending tracts carry efferent/motor signals within the CNS

    • right hand side of brain, carried down via descending tract, then some of the signals cross over to left side

  • left side of the brain moves right side of the body


<ul><li><p>opposite side</p></li><li><p>most signals between the body and the brain (and vice versa) are contralateral</p></li><li><p>ascending tracts carry afferent/sensory signals within the CNS </p><ul><li><p>in from lefthand side, crossing over to righthand side of spinal cord, up to the right somatosensory cortex</p></li></ul></li><li><p>descending tracts carry efferent/motor signals within the CNS</p><ul><li><p>right hand side of brain, carried down via descending tract, then some of the signals cross over to left side</p></li></ul></li><li><p>left side of the brain moves right side of the body</p></li></ul><p></p>
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ipsilateral

  • same side

  • signals stay/exit on the same side of the CNS


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what does the spinal cord directly connect to?

the hindbrain

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hindbrain main components

  • medulla oblongata

  • pons

  • cerebellum


<ul><li><p>medulla oblongata</p></li><li><p>pons</p></li><li><p>cerebellum</p></li></ul><p></p>
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medulla oblongata

regulates breathing, HR, blood pressure

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pons

communicates between medulla, cerebellum, and forebrain

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cerebellum

coordinates motor behaviors

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forebrain/cerebrum

  • controls “higher” processes


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cerebrum structure

  • frontal lobe

  • temporal loba

  • parietal lobe

  • occipital lob


<ul><li><p>frontal lobe</p></li><li><p>temporal loba</p></li><li><p>parietal lobe</p></li><li><p>occipital lob</p></li></ul><p></p>
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corpus callosum

  • white matter tract

  • connects the left and right cerebral hemispheres


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cerebral cortex

  • surface gray matter

  • can be divided into functional areas


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motor areas in the frontal lobe

  • premotor cortex

  • primary motor cortex


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premotor cortex

coordinates movements of groups of muscles

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primary motor cortex

  • controls discrete skeletal muscles

  • stimulation results in specific movements on opposite side of body


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what happens when the premotor cortex is damaged?

loss of skill that can often be relearned

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what happens when the primary motor cortex is damaged?

  • paralysis of voluntary movements that are rarely regained

  • reflexes remain intact


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somatosensory areas in the parietal lobe

  • primary somatosensory cortex

  • somatosensory association area


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primary somatosensory cortex

primary input from touch, temperature, and pain receptors in skin & muscle on opposite side of body


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what happens when the primary somatosensory cortex is damaged?

loss sensation that rarely returns

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somatosensory association area

  • interpretation of sensation

  • integration with memory

  • ex: reach into pocket


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what happens when the somatosensory association area is damaged?

loss of identification that can be relearned

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ex of damaged somatosensory cortex vs somatosensory association area

normal: reach into pocket w/ key → recognize the ridges in denim material and coldness from key; recognize that it is a key

damaged: reach into pocket w/ key → cannot feel the coldness from key and cannot recognize that it is a key BUT can learn to recognize that it’s a key

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visual areas of the CNS

  • primary visual cortex

  • visual association areas

  • far more ipsilateral signals than in most other systems


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primary visual cortex

  • primary input from optic tracts

  • activated by visual stimuli


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visual association areas

integration and perception

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limbic system and 5 functions (actually 7)

  • many functionally important structures are situated below the cerebral cortex

  • functions: smell, homeostasis, emotions, fear & aggression, learning & memory, relay station


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diencephalon key structures

the thalamus and hypothalamus

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thalamus

  • filters and sorts sensory inputs

  • routes information


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hypothalamus

  • diverse set of homeostatic functions

  • regulates pituitary gland

  • plays a key role in homeostatic regulation


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hypothalamus: homeostatic regulation

  • invovled in the stress response

    • HPA (hypothalamus, pituitary, adrenal) axis

  • regulates food intake

  • regulates body temperature

  • helps maintain ion and water balance

  • regulates circadian rhythms


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homeostasis requires what?

the balancing of sympathetic and parasympathetic nervous systems

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sympathetic nervous system

  • most active during stress or physical activity

  • “fight or flight” response

  • increases heart rate & breathing, directs blood to working muscles during exerise


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parasympathetic nervous system

  • most active during periods of rest

  • “resting and digesting”

  • redirects energy toward maintenance activities, such as digestion


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sympathetic and parasympathetic neurons differ structurally and functionally

sympathetic:

  • preganglionic neurons have cell bodies in the CNS and axons that extend to their ganglion

  • postganglionic neurons release entirely different NT (neuroepinepherine)

  • ganglion near the CNS and long postganglionic axon

parasympathetic:

  • postganglionic neurons have cell bodies in the ganglion and axons that extend from the ganglion to their target

  • long preganglionic axon and ganglion near target organ


  • receptors that respond to ACh are different for each


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acetycholine (ACh)

  • first NT to be discovered

  • synthesized at axon terminals of “cholinergic” neurons

    • making and releasing primarily ACh

  • NT released at neuromuscular junction and parts of central and peripheral nervous systems

  • ACh has 2 types of receptors (AChR): nicotinic and muscarinic


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acetylcholine receptors

nicotinic AChR and muscarinic AChR

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nicotinic AChR

  • ionotropic

    • when ACh binds, the channel will directly open and allow Na+ to enter

  • excitatory

  • produce EPSP in postsynaptic neuron

  • found in autonomic and motor neurons

  • non-specific cation channel (most often conduct Na+)


<ul><li><p>ionotropic</p><ul><li><p>when ACh binds, the channel will directly open and allow Na+ to enter</p></li></ul></li><li><p>excitatory</p></li><li><p>produce EPSP in postsynaptic neuron</p></li><li><p>found in autonomic and motor neurons</p></li><li><p>non-specific cation channel (most often conduct Na+)</p></li></ul><p></p>
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muscarinic AChR

  • metabotropic

    • G-protein coupled receptors (GPCRs)

    • linked to “second” messenger systems

  • found in smooth and cardiac muscle, glands, and CNS

  • excitatory or inhibitory (depending on receptor type and G-protein pair)


<ul><li><p>metabotropic</p><ul><li><p>G-protein coupled receptors (GPCRs)</p></li><li><p>linked to “second” messenger systems</p></li></ul></li><li><p>found in smooth and cardiac muscle, glands, and CNS</p></li><li><p>excitatory or inhibitory (depending on receptor type and G-protein pair)</p></li></ul><p></p>
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norepinephrine/noradrenaline


  • part of catecholamine: family of signaling chemicals made in your body that includes dopamine, norepinephrine, and epinephrine

  • like epinephrine/adrenaline, but functions mostly as a sympathetic neurotransmitter

    • triggers immediate, targeted responses vs epinephrine is released by adrenal glands directly into bloodstream to circulate everywhere and produce broad, body-wide emergency effects


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changes in action potential frequency of sympathetic neurons alter what?

the target response

  • increase in sympathetic neurons → increase in AP firing rate → blood vessel constricts (in given example)

  • decrease sympathetic neurons → decreased AP firing rate → blood vesssel dilates


<p>the target response</p><ul><li><p>increase in sympathetic neurons → increase in AP firing rate → blood vessel constricts (in given example)</p></li><li><p>decrease sympathetic neurons → decreased AP firing rate → blood vesssel dilates</p></li></ul><p></p>
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adrenergic receptors

  • receptor that norepinephrine/noradrenaline binds to

  • also respond to epinephrine from the adrenal gland

  • metabotropic

    • GPCRs linked to ion channel function via G-proteins

  • found throughout the body

  • diverse effects based on receptor subtype


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adrenergic receptors subtype alpha1

  • location: smooth muscle of blood vessels to skin and gut

  • pathway: Gq → PLC (phospho-lipase C)

    • breaking down of PIP2 into IP3 and DAG

    • further consequences related to Ca2+ (activation of Ca2+ channels)

  • effect: vasoconstriction

    • smooth muscles will contract and make diameter of blood vessels smaller


<ul><li><p>location: smooth muscle of blood vessels to skin and gut</p></li><li><p>pathway: Gq → PLC (phospho-lipase C)</p><ul><li><p>breaking down of PIP2 into IP3 and DAG</p></li><li><p>further consequences related to Ca2+ (activation of Ca2+ channels)</p></li></ul></li><li><p>effect: vasoconstriction</p><ul><li><p>smooth muscles will contract and make diameter of blood vessels smaller</p></li></ul></li></ul><p></p>
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adrenergic receptors subtype alpha2

  • location: adrenergic axon terminals

  • pathway: Gi (inhibitory G protein) → ↓cAMP

    • when noroepinephrine binds, the G protein is Gi

    • inactive adenocyclase which is normally converting ATP to cAMP

    • decreases cAMP

    • inactives Ca2+, which is needed for noroepinephrine release

  • effect: inhibit NE release


<ul><li><p>location: adrenergic axon terminals</p></li><li><p>pathway: Gi (inhibitory G protein) → ↓cAMP</p><ul><li><p>when noroepinephrine binds, the G protein is Gi</p></li><li><p>inactive adenocyclase which is normally converting ATP to cAMP</p></li><li><p>decreases cAMP</p></li><li><p>inactives Ca2+, which is needed for noroepinephrine release</p></li></ul></li><li><p>effect: inhibit NE release</p></li></ul><p></p>
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adrenergic receptors subtype beta1&2

  • location:

    • beta1 - heart

    • beta2 - smooth muscle of blood vessels to heart & skeletal muscle

  • pathway: Gs (stimulatory G protein) → ↑cAMP’

    • Gs active adenocyclcase which will convert more ATP into cAMP

    • activates Ca2+ channels, increasing Ca2+, increasing rate and strength of contraction

  • effect:

    • increase heart rate and contraction strength

    • vasodilation


<ul><li><p>location:</p><ul><li><p>beta1 - heart</p></li><li><p>beta2 - smooth muscle of blood vessels to heart &amp; skeletal muscle</p></li></ul></li><li><p>pathway: Gs (stimulatory G protein) → ↑cAMP’</p><ul><li><p>Gs active adenocyclcase which will convert more ATP into cAMP</p></li><li><p>activates Ca2+ channels, increasing Ca2+, increasing rate and strength of contraction</p></li></ul></li><li><p>effect:</p><ul><li><p>increase heart rate and contraction strength</p></li><li><p>vasodilation</p></li></ul></li></ul><p></p>
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the adrenal medulla is innverated by what?

the sympathetic nervous system only

  • preganglionic sympathetic neuron release ACh → binds to receptor in chromaffin cells → release epinephrine → released into blood stream as a hormone


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adrenal medulla innveration

  • the chromaffin cells release epinephrine into the blood stream in response to acetycholine from preganglionic sympathetic neurons

  • the developmental and evolutionary origins suggest chromaffin cells are modified post-ganglionic neurons


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differences in receptor subtypes among effector organs

  • effector organs express different metabotropic adrenergic receptors

  • differences explain the diverse effects of epinephrine/norepinephrine in various tissues


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what systems regulate homeostatic processes?

the endocrine, parasympathetic, and sympathetic nervous systems

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sensory systems

  • detect stimuli and send info to an integrating center

  • receives a stimulus → convert into neuronal signal → carried via afferent neurons into CNS


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sensory stimuli

  • detected in neurons or accessory cells

  • generator and receptor potential


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generator potential

  • a graded potential that occurs in a sensory neuron as a direct result of the stimulus

  • dendrite of sensory neuron has receptor for stimulus embedded in plasma membrane→ direct depolarziation of primary afferent neuron, creating a generator potential

  • if this depolarization reaches the neuron’s trigger zone with enough strength, it initiates an AP that travels along axon to CNS

  • **the cell detecting the stimulus and the neuron sending the signal to the brain are the same single cell - direct pathway


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receptor potential

  • a graded potential that occurs in a specialized receptor cell (accessory cell) due to a sensory stimulus and then must be transmitted to the neuron

  • stimulus triggers a receptor protein that is localized in an accessory cell, causing depolarization called a receptor potential

  • this depolarization triggers an influx of Ca2+ → vesicles release NT via exocytosis

  • the NT bind to the receptors on the dendrite of an adjacent afferent neuron, inducing a secondary graded potential in that neuron

    • does not actually fire AP

  • the detector cell is a separate accessory cell that must communicate via chemical neurotransmitters to activate the sensory neuron - indirect pathway


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sensory receptors can be classified by their stimulus modality (6)

  1. chemoreceptors: detect the presence of chemicals in the environment

  2. mechanoreceptors: detect pressure and movement, including proprioception (detection of body and space)

  3. photoreceptors: detect light

  4. thermoreceptors: detect temperature

  5. electroreceptors: detect electric fields

  6. magnetoreceptors: detect magnetic fields


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stimulus encoding and 4 impt features

  • sensory receptors convert info about the stimulus into changes in membrane potential and eventually action potentials

  • encode 4 important features:

    • stimulus modality - signal pathways

    • stimulus location - receptive field

    • stimulus intensity - frequency/strength

    • stimulus duration - tonic & phasic receptors


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sensory pathways can encode stimulus modality

  • a particular afferent neuron is associated with one modality of receptor and stimulus (adequate stimulus)

  • each afferent neuron stimulates activity within a particular neural pathway

  • perception based on pathway activated, not the stimulus identity

    • ex: close eyes, rub, open - what do u see? speckled light pattern

      • this is a response to pressure stimulus - perceieve light even tho stimulus was pressure



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receptive field

  • region of the sensory surface that causes a response when stimulated

  • varies in size and therefore acuity

    • smaller receptive fields allow more precise localization of the stimulus (i.e. greater spatial acuity)


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receptive field and localization of stimulus

receptive fields encode stimulus location based on the signal pathway

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acuity

ability to resolve fine detail of a stimulus

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lateral inhibition

  • signals from neurons at the center of the receptive field inhibit surrounding neurons

  • improves acuity

  • enhances contrast: magnifies the difference in firing rates between the central point of stimulus and surrounding area

  • decreases “noise”: mutes weak, redundant background signals from surrounding neurons

  • improves edge detection/boundaries: allows the CNS to clearly identify where a stimulus begins and ends


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action potential frequency encodes signal intensity

  • sensory neurons code stimulus intensity by changes in action potential frequency

  • ex: increased stimulus → increased frequency of action potentials


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sensory receptors

  • encode a limited range of stimulus intensities

  • sensory neurons code stimulus intensity by changes in action potential frequency

    • ex: strong stimuli → high frequency

  • dynamic range

  • increase in magnitude of graded potential or frequency of AP


<ul><li><p>encode a limited range of stimulus intensities</p></li><li><p>sensory neurons code stimulus intensity by changes in action potential frequency</p><ul><li><p>ex: strong stimuli → high frequency</p></li></ul></li><li><p>dynamic range</p></li><li><p>increase in magnitude of graded potential or frequency of AP</p></li></ul><p></p>
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dynamic range

  • range of stimulus intensities over which a receptor exhibits changing responses

  • threshold: weakest stimulus that produces a response in a receptor

  • saturation: top of the dynamic range (maximal response - won’t change even if stimulus intensity increases)


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dynamic range and discrimination

  • large dynamic range = poor sensory discrimination

    • large change in stimulus intensity causes a small change in AP frequency

  • narrow dynamic range = good sensory discrimination

    • small changes in stimulus intensity causes a large change in AP frequency


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sensory discrimination

  • the ability to detect differences between stimuli

  • improves by distributing responses amongst different receptors

  • range fractionation: different receptors cover different parts of the stimulus intensity spectrum

    • expands the range of intensities the sensory intensities the sensory surface or system responds to


<ul><li><p>the ability to detect differences between stimuli</p></li><li><p>improves by distributing responses amongst different receptors</p></li><li><p><strong>range fractionation</strong>: different receptors cover different parts of the stimulus intensity spectrum</p><ul><li><p>expands the range of intensities the sensory intensities the sensory surface or system responds to</p></li></ul></li></ul><p></p>
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range fractionoism

different receptors cover different parts of the stimulus intensity spectrum


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logarithmic encoding

  • some receptors use logarithmic encoding

  • logarithmic encoding of intensity allows for increased dynamic range without completely sacrificing discrimination

  • better discrimination in lower range


<ul><li><p>some receptors use logarithmic encoding</p></li><li><p>logarithmic encoding of intensity allows for increased dynamic range without completely sacrificing discrimination</p></li><li><p>better discrimination in lower range</p></li></ul><p></p>
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tonic and phasic receptors

  • encode stimulus duration

  • tonic receptors respond for the entire duration of a stimulus

  • phasic receptors respond to changes in a stimulus


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phasic receptors

  • respond to changes in a stimulus

  • can encode stimulus changes in several ways

  • pic: on set (first column), combo, off


<ul><li><p>respond to changes in a stimulus</p></li><li><p>can encode stimulus changes in several ways</p></li><li><p>pic: on set (first column), combo, off</p></li></ul><p></p>
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sensory adaptation

  • decreased response to a stimulus as duration increases

  • tonic receptors are typically slow adapting

  • phasic receptors adapt so quickly that they produce APs only when the stimulus changes

  • for prolonged stimuli, sensory adaptation can continue until the stimulus is tuned out


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AP frequency and prolonged stimulus

AP frequency often decreases

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photoreceptors

convert light energy into changes in membrane potential

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photoreceptive opsins

  • seven-membrane-spanning GPCRs

  • opsins localize to membranes in the outer segments of vertebrate photoreceptors


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phototransduction

occurs thorugh chromophore isomerization (chemical goes from cis to trans conformation)

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summary of light-induced events

  • opsins covalently bind vitamin-A derived choromophores

  • photons cause isomerization of the choromophore

  • isomerization of chromophore leads to changes in the opsin

    • conformational change in opsin

    • dissociation of choromophore from obsin (“bleaching”)

  • G-protein singnaling events cause changes in membrane potential


<ul><li><p>opsins covalently bind vitamin-A derived <strong>choromophores</strong></p></li><li><p>photons cause <strong>isomerization</strong> of the choromophore</p></li><li><p>isomerization of chromophore leads to <strong>changes in the opsin</strong></p><ul><li><p>conformational change in opsin</p></li><li><p>dissociation of choromophore from obsin (“bleaching”)</p></li></ul></li><li><p>G-protein singnaling events cause changes in membrane potential</p></li></ul><p></p>
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2 classes of photoreceptor are found throughout the animal kingdom

  1. rhabdomeric receptors

    1. rhabdomeric PRs were recently discovered in vertebrates too → these PRs help entrain our internal clocks to environmental light/dark cycles

  2. cilary receptors

    1. rods and cone are ciliary receptors (vision)

both have evolved multiple times (not clustered when looking at evolutionary tree)



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rhabdomeric photoreceptors signal thorugh Gq

  1. 11-cis 3-hydroxy retinal absorbs light and isomerizes into all trans 3-hydroxy retinal

  2. all trans 3-hydroxy retinal dissociates from opsin

  3. activated opsin activates a Gq protein

  4. activated Gq activates PLC (phospholipase C), converting PIP2 to DAG and IP3

  5. DAG activates a TRP cation channel (non-selective)

    1. gated by IP3 and DAG

  6. Ca2+ and Na+ enter the cell, depolarizing it


<ol><li><p>11-cis 3-hydroxy retinal absorbs light and isomerizes into all trans 3-hydroxy retinal</p></li><li><p>all trans 3-hydroxy retinal dissociates from opsin</p></li><li><p>activated opsin activates a Gq protein</p></li><li><p>activated Gq activates PLC (phospholipase C), converting PIP2 to DAG and IP3</p></li><li><p>DAG activates a TRP cation channel (non-selective)</p><ol><li><p>gated by IP3 and DAG</p></li></ol></li><li><p>Ca2+ and Na+ enter the cell, depolarizing it</p></li></ol><p></p>
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ciliary photoreceptors signal through G¡/transducin

  1. 11-cis Retinal absorbs light and isomerizes into all-trans retinal

  2. all-trans retinal dissociates from opsin

  3. activated opsin activates the G¡ protein (inhibitory G protein) transducin

  4. transducin actives PDE (phosphodiesterose), which converts cGMP to GMP

    1. signaling molecule that can open CNG (cyclic nucleotide-gated) channel

  5. the decreased cGMP closes a Na+ channel

  6. Na+ entry decreases, hyperpolarizing the cell


<ol><li><p>11-cis Retinal absorbs light and isomerizes into all-trans retinal</p></li><li><p>all-trans retinal dissociates from opsin</p></li><li><p>activated opsin activates the G¡ protein (inhibitory G protein) transducin</p></li><li><p>transducin actives PDE (phosphodiesterose), which converts cGMP to GMP</p><ol><li><p>signaling molecule that can open CNG (cyclic nucleotide-gated) channel</p></li></ol></li><li><p>the decreased cGMP closes a Na+ channel</p></li><li><p>Na+ entry decreases, hyperpolarizing the cell</p></li></ol><p></p>
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mammalian eye

  • allows formation of a bright, focused image

  • light enters through front of eye and hits cornea → travels through pupil (hole in iris) → hits the lens, which is held in place by ciliary body → lens does fine tuning so light gets targeted to fovea (specialized part in retina where rods/cones located) → activation of photoreceptors → light passes through and hits choroid (absorbs any remaining light energy) → exit eye via optic disk through optic nerve

  • muscle fibers of the iris change the pupil diameter and control the amount of light entering the eye

  • the cornea refracts light and focuses it onto the lens, which is responsible for fine-tuning the focus onto the retina

    • the lens changes shape depending on the distance of the light source in a process called accommodation

  • light passes through the retina and excites the photoreceptors

  • the choroid is a pigmented layer that absorbs the light


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muscle fibers of the iris

  • change the pupil diameter in response to light

    • controled by SNS and PNS

  • radial muscle layer (like the rays of sun, spreads out)

    • dilates pupil via SNS

  • circular layer of muscles

    • contracts via PNS


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choroids of nocturnal animals

  • contain a reflective layer

  • the tapetum lucidum reflects and amplifies dim light in nocturnal animals and make their eyes “glow”


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cornea and lens

  • convex lenses that direct light onto the retina

  • when parallel light waves hit the lens, it will cause refraction that converges the waves onto a single point

  • most refraction occurs at the cornea

  • the lens is responsible for fine-tuning

  • most of the focusing is done by the cornea


<ul><li><p>convex lenses that direct light onto the retina</p></li><li><p>when parallel light waves hit the lens, it will cause refraction that converges the waves onto a single point</p></li><li><p>most refraction occurs at the cornea</p></li><li><p>the lens is responsible for fine-tuning</p></li><li><p>most of the focusing is done by the cornea</p></li></ul><p></p>
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accommodation

  • referes to the ability of the eye to focus light from different distances

  • during accommodation, the cillary muscle contracts, the ligaments slcak, and the lens bulges (to change focal length)

  • distant object

    • enters eye as parallel rays

    • short focal length

  • nearby object

    • enters eye as nonparallel rays

    • increased focal length (point of convergence is beyond the retina → dispersed light hitting retina → not focused)

  • nearby object w/ accommodation

    • focal length restored


<ul><li><p>referes to the ability of the eye to focus light from different distances</p></li><li><p>during accommodation, the cillary muscle contracts, the ligaments slcak, and the lens bulges (to change focal length)</p></li><li><p>distant object</p><ul><li><p>enters eye as parallel rays</p></li><li><p>short focal length</p></li></ul></li><li><p>nearby object</p><ul><li><p>enters eye as nonparallel rays</p></li><li><p>increased focal length (point of convergence is beyond the retina → dispersed light hitting retina → not focused)</p></li></ul></li><li><p>nearby object w/ accommodation</p><ul><li><p>focal length restored</p></li></ul></li></ul><p></p>
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rods and cones

  • located at the back of the retina

  • few layers of cells light must pass through in retina to hit the photoreceptors

    • activate G protein coupled receptor → cause activation of PDE → cause hyperpolarization

  • decrease inhibitory NT (glutamate) release

    • activation of bipolar cells → activation of retinal ganglion cells → carry signal out via optic disk and optic nerve


<ul><li><p>located at the back of the retina</p></li><li><p>few layers of cells light must pass through in retina to hit the photoreceptors</p><ul><li><p>activate G protein coupled receptor → cause activation of PDE → cause hyperpolarization</p></li></ul></li><li><p>decrease inhibitory NT (glutamate) release </p><ul><li><p>activation of bipolar cells → activation of retinal ganglion cells → carry signal out via optic disk and optic nerve</p></li></ul></li></ul><p></p>