IPHY 3430 Exam 2 [Nervous] Flashcards

(88 cards)

1
Q

Nervous system

A
  • communication system
    -coordinates body function; electrical signals[graded potentials & action potentials]
    chemical signals; neurocrines[neurohormone, neurotransmitter, neuromodulators]
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2
Q

organization of NS

A
  • CNS
  • PNS: sensory[afferent] & motor[efferent; somatic division & autonomic division(sympathetic and parasympathetic branch)]
  • Enteric Nervous system(digestion)
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3
Q

Nervous system cells

A

neurons: basic signaling molecule

glial cells: provide support for neurons(many types of glial cells bu we focus on oligodendrocytes and schwann cells)

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4
Q

3 functional groups of neurons

A

afferent(sensory)
interneuron(there can be many or none)
Efferent (motor) neuron

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5
Q

Organization of a neuron

A

Dendrtite= input (receive incoming signals)
soma(cell body) = contains nucleus
trigger zone = “initial segement”; integration
axon = conduction(long distance); myelin and nodes of ranvier
Presynaptic (axon) terminal = output(talk to target cell)

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6
Q

Oligodendrocytes vs schwann cells

A

oligodendrocytes: form myelin in the CNS, wrap up to 15 axons
schwann cells: form myelin in PNS, wrap 1 axon

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7
Q

how are neurons connected? (labeled lines)

A

presynaptic cell: delivers signal at synapse

postsynaptic cell: receives signal at synapse

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8
Q

2 Electrical signals in neurons

A

Graded potential = local signals, purpose is to carry info from input region to trigger zone
Action potential = long distance signals, purpose is to carry info to presynaptic axon terminal

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9
Q

Integrative action

A

where there is both action and graded potentials

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10
Q

are electrical signals temporary changes in membrane potential?

A

yes, due to temporary (transient) changes in membrane permeability via gated ion channels.
- chemically-, mechanically- , voltage- gated.

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11
Q

Do electrical signals appreciably change ion concentrations ?

A

No, they do change separation of charge across the membrane(membrane potential)

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12
Q

Graded Potentials

A
  • originate in input region due to opening of gated channels

- decrease in amplitude(lose “strength”, “decay”) as travel

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13
Q

excitatory vs inhibitory

A

*Graded potentials can be both
excitatory- depolarize cell & make it easier to produce action potential
inhibitory- hyperpolarize cell & make it harder to produce action potential

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14
Q

different names for graded potentials

A

receptor potential: input region of sensory neuron
synaptic potential (Excitatory postsynaptic potential[EPSP], inhibitory postsynaptic potential [IPSP]): input region of interneuron and motor neuron
End-plate potential: input region of skeletal muscle

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15
Q

graded potential strength and duration

A

graded potentials vary in amplitude & duration to convey information about stimulus amplitude & duration.

  • amp: typically 0.1-10mV
  • duration: typically 2-10 msec
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16
Q

Where are graded potentials summated?

A

Graded potentials travel to trigger zone (integrative

site) & summate.
- typical neuron receives ~1000-10,000 inputs
- decision: action potential

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17
Q

integration at trigger zone from graded potential

A

determines whether action potentials produced & information is passed along

  • action potential threshold [subthreshold, suprathreshold]
  • both action and graded potentials at trigger zone(transition from local to long distance)
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18
Q

Purpose of action potentials

A

carry info from trigger zone to synapse(presynaptic terminal)
- log distance; dont decrease in amplitude(strength as propagate, “regenerated”
all-or- none(summate)- decisions been made.
typically ~1ms,~100mV but can vary based on ion flow.

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19
Q

how to Action potentials convey info?

A

Frequency: codes for stimulus amplitude (intensity,strength)
Duration of spike train: codes for stimulus duration

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20
Q

How are action potentials produced

A

Gated ion channels; produced by sequential opening & closing of voltage -gated ion channels.
- you need to let it rest before you try and produce another action potential, can’t summate

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21
Q

Gated ion channels for action potentials

A

Hodgkin-Huxley channels:
H-H Na+: closed(resting), open, inactive(refractory)
- time dependant
H-H K+ : closed, open

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22
Q

Action potential threshold

A

Action produced when trigger zone is depolarized above threshold because of positive feedback, Na+ comes in and tries to depolarize into its equilibrium potential.

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23
Q

Similarities between Na+ and K+ channels

A

differences: time responds to stimulus, reason ion stops flowing, # gates- inactivation- time(~1 msec)
similarities: voltage dependant; depolarize (~15-20mV) -> open - repolarize -> closed

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24
Q

Termination of positive feedback cycle

A

Two processes to repolarize cell

1) inactivation of voltage - gated Na+ channels
2) opening of voltage- gated K+ channels

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25
Refractory periods
* not all channels reset at the same time Absolute refractory: when there is no chance to summate an action potential relative refractory period: some channels are ready but some are not, you can get a small action potential. Na+ channels are time dependant so not all of them are ready, - to produce full action potential it takes about 2 msec
26
Action potential propagation
like dominos, the same action potential does not move, it just triggers the next one - voltage- gated Na+ channels open & Na+ flows in, depolarizing that part of the axon; passive current flow depolarizes neighboring region[like water flowing along a pipe]
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Speed of action potential
2 mechanisms increase conduction velocity. - diameter of axon; the bigger the faster - myelination, prorogations are faster when there is myelin on that section. Nodes of ranvier have teh ion channels so it is slower on those portions
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saltatory conduction
myelinated axons | - nodes of ranvier; no nodes, where voltage gated channels and regeneration of action potential happens
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how do action potentials convey info to synapse
action potentials propagate unfailingly over long | distances to output region (synaptic/axon terminal)
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types of synapses
electrical: gap junctions, synchronize activity, rapid bidirectional signal conduction Chemical: majority of synapses, most neurotransmitters stored in vesicles &exocytosed due to action potential [neurotransmitter diffuses across synaptic cleft.], slower but more flexible & allows amplification
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purpose of action potential
open voltage gated Ca++ channels for exocytosis. | - uses hydrogen ion gradient and uses it as secondary active transport for exocytosis.
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Neurotransmitter/ neurocrine secretion
-Release of neurotransmitter/neurocrine depends on frequency of action potentials, & duration of spike train -Major neurocrines of peripheral nervous system (PNS): acetylcholin(ACh), norepinephrine (NE), epinephrine (E)
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types of postsynaptic receptors
nicotinic, muscarinic, AchR - 2 types: ionotropic (directly gated, channel protein) • metabotropic (indirectly-gated, GPCR/RE) - response maybe be excitatory or inhibitory • EPSP/IPSP – excitatory/inhibitory post-synaptic potential EPSP: depolarization (Na+) IPSP: hyperpolarization (Ca++)
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Termination of neurotransmitter activity
inactivate, reuptake, diffuse away. pump out Ca++
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Afferent Division of PNS
Detects, encodes & transmits signals about internal & external environment to CNS
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sensory receptors
classified based on nature of stimulus(type of energy) that receptor responds to & transduces
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types of senses
special senses, somatic senses, visceral senses
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special sense
have specialized organs devoted to them: eye, ear, nose, tongue; taste, vision, hearing, equilibrium, smell.
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somatic senses
somatosensory receptors - collect information from surface of body (cutaneous sensations), and muscles & joints (proprioceptive sensations => body position) • cutaneous: touch, pain, skin temperature • proprioception: e.g., muscle length & force, joint position
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visceral sense
• interoceptors sense/detect stimuli within internal organs (viscera) such as blood vessels, gut, etc. • e.g., chemoreceptors, baroreceptors, osmoreceptors • monitor internal environment, e.g., blood glucose, blood osmolarity, blood pressure, internal temperature
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phasic vs, tropic receptors
Phasic: rapid adapting, on off cells, don't tell you how long something has been on/off for. just tells you something is on/off Tonic: slowly adapting, stays active throughout the entire time of stimulus
42
Receptive fields
Region w/in which a sensory neuron sense a stimulus: how you keep track of where signal came from.
43
Sensory transduction
Stimulus alters receptor cells permeability leading to a graded potential - transduction occurs via : ionotropic and metabotropic channels
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ionotropic channels
directly gated: mechanical, chemical, voltage
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Metabolic channels
indirectly gated: GPCR, receptor enzyme.
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Tastant transduction: why don't we get confused on what flavors are which?
each taste cell only sense one type of ligand: salt, sour, bitter, sweet, or umami G-protein: metabotropic[bitter, sweet, umami, fat] tastant: transducing channels, ionotropic[salt(NA+), sour(H+)
47
spinal cord organization for afferent signals.
spinal cord is organized to keep track of information -somatotopy: "body map" Sensory spinal cord: dorsal root, dorsal horn[ somatic, visceral]
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Decussation
"crossover" sensory info decussates (crosses over) to other side of nervous system • "upper" medulla: fine touch, proprioception, vibration -dorsal column-medial lemniscus tract • "lower" spinal cord: nociception (pain), temperature, coarse touch - anterolateral tract
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Thalamus
* relay station - (with exception of olfaction) | * many nuclei – each for one type of sensory information
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Somatosensory organization
Somatosensory projections from body maintain body map - CNS integrates sensory information - highest sensory signals when we are born come from the mouth and hands, so that takes a big part of the min-body map
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Brain areas
``` CEREBELLUM FOREBRAIN: - cerebrum ------cerebral cortex; frontal lobe, parietal, occipital, temporal, ------basal nuclei (voluntary movement) -diencephalon; hypothalamus, thalamus BRAIN STEM - medulla oblongata - pons - midbrain[eye movement] ```
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Autonomic control centers
Hypothalamus: receives visceral sensory inputs & control autonomic sys, temp control, water balance, eating behavior Pons & medulla: control autonomic sys (ANS) output to periphery; bladder control, sec respiratory control, BP, respiratory center
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Cerebellum
muscle(voluntary movement)
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where is sensory information processed?
cerebral cortex - parietal lobe: info from skin, musculoskeletal system, viscera, and taste buds - frontal lobe: coordinates info from other association areas, controls some behaviors - temporal lobe: auditory association area, taste and smell - occipital lobe: vision
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Efferent (motor) divisions
somatic and autonomic
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what part of the brain controls somatic motor neuron?
Motor cortex; then descends spinal cord - corticospinal tracts: most cross (decussate)at medulla(pyramidal tract) - somatotopy maintained
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what does somatic motor division control?
SKELETAL MUSCLE somatic (alpha) motor neurons • control skeletal muscle contractions (mostly voluntary) • tonic • neuron originates in CNS (ventral horn) • leave ventral horn via ventral root to synapse onto skeletal muscle
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Neuromuscular junction
somatic(a) motor neuron releases acetylcholine - always excitatory Skeletal muscle fiber membrane (sarcolemma) contain nicotinic acetylcholine receptors (nAChR)
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end plate potential
Binding of acetylcholine (ACh) to nicotinic receptor (nAChR) opens ion channels leading to depolarization of muscle membrane - excitatory (Na+) ** graded potential = end plate potential
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Events at Neuromuscular junction
End-plate potential causes voltage-gated Na+ channels to open in muscle membrane (sarcolemma) leading to muscle (sarcolemmal) action potential .... ->muscle contraction
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Life cycle of acetylcholine at neuromuscular junction
acetyltransferase(enzyme) - acetyl CoA & choline - acetyl CoA comes from citric acid cycle - choline comes from diet(recycled)
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Termination of acetylcholine pathway
Acetylcholinesterase (AChE) | - breaks it down to acetate and choline
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Neurocrine Naming
Need to differentiate cell that makes & releases signal versus cell that has receptors for signal examples: • cholinergic (relates to acetylcholine) • cholinergic neuron – makes & releases acetylcholine as signal • cholinergic receptor – binds & responds to acetylcholine • subtypes: nicotinic, muscarinic • adrenergic (relates to epinephrine/norepinephrine) • adrenergic neuron - makes & releases E / NE as signal • adrenergic receptor – binds & responds to E / NE • subtypes: alpha, beta • dopaminergic, serotonergic, GABAergic, glycinergic, histaminergic, glutamatergic,….
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what does Autonomic neurons control?
``` Control - cardiac & smooth muscles - many glands - lymphoid & some adipose tissue Mostly involuntary - regulate/influence visceral functions ```
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Autonomic Division branches
Parasympathetic and sympathetic Most effectors connected to both branches (antagonistic control) • excitatory & inhibitory effects (unlike somatic branch) • act simultaneously • shifts in predominance due to mental & physiological states • autonomic tone* (background activity; balance between 2 branches)
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Autonomic Nervous system
creates autonomic, endocrine, & behavioral responses - influenced by: cerebral cortex, limbic system works closely w/ endocrine system to maintain homeostasis
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Antagonistic control of autonomic NS
Most internal organs are under antagonistic control. Exceptions - only innervated by sympathetic branch (tonic) • (sweat glands) • smooth muscle of most blood vessels
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Autonomic pathways consist of...
All autonomic pathways consist of 2 neurons in series 2 neurons that synapse in an autonomic ganglion CNS -> preganglionic neuron -> autonomic ganglion (mini- integrating center) -> postganglionic neuron -> target tissue
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2 autonomic neuron pathways
sympathetic ganglia and parasympathetic ganglia
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sympathetic ganglia
* close to spinal cord * short preganglionic neurons * thoracic & lumbar segments * long postganglionic neurons
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parasympathetic ganglia
* vagus nerve is major tract: contains ~75% of fibers * located primarily on or near target organs * long preganglionic neurons * brain stem & sacral region * short postganglionic neurons
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ANS: Neurotransmitters and receptors
receptors: cholinergic [ nicotinic and muscarinic ] and adrenergic [ alpha and beta ] - sympathetic pathways use CNS -> acetylcholine release from preganglionic neuron -> nicotinic receptor on autonomic ganglion-> norepinephrine released from postganglionic neuron -> target cell. - parasympathetic use CNS ->preganglionic neuron -> acetylcholine -> nicotinic receptor on autonomic ganglia -> Acetylcholine released from postganglionic neuron -> GPCR
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Varicosities
where autonomic post ganglionic neurons end. It contains neurotransmitter & release it over the surface of the target cell
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Life cycle of norepinephrine at sympathetic neuroeffector junction
neuro effector junction: catecholamines are derived from tyrosine(amino acid) -> pump norepinephrine into vesicles by secondary active transport -> the rest is the same as the neuromuscular junction
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pancreas and the ANS
Pancreas is innervated by both branches, para and sympathetic. Parasympathetic: increases activity due to food in digestive tract - insulin secretion via IP3-Ca++ pathway [ feedforward response] Sympathetic : inhibits the insulin secretion by decreasing cAMP - effect; increased blood glucose available to fuel muscle activity for fight or flight
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Arterioles: receptor type determination
alpha and Beta adrenergic receptors on arterioles: - B2 receptors cause vasodilation- decreases cAMP - a receptors cause vasoconstriction - activates PLC certain organs during fight or flight with receives one of the responses, muscles will dilate, urinary will constrict
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what stays longer; epinephrine or norepinephrine?
Norepinephrine
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termination of Norepinephrine
diffuses away or use active transport to move it back into the cell it came from or neighboring glial cells
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Adrenal Medulla
a specialized neuroendocrine gland that secretes epinephrine into blood
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reflexes
involuntary responses triggered by a sensory stimulus
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classifications of reflexes
* efferent division: somatic vs. autonomic * integrating region in CNS: spinal (spinal cord) vs. cranial (brain) * time develops: innate (born - e.g., patellar tendon) vs. learned (conditioned) (acquired thru experience - e.g., Pavlov’s dog) * number of neurons: monosynaptic vs. polysynaptic
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Autonomic reflexes
``` involve autonomic neurons & targets (internal organs) ex: • urination/defecation • salivating • vomiting • sneezing • coughing • swallowing • gagging • blushing • heart rate • blood pressure ****THEY CAN BE LINKED TO EMOTION[ GUT FEELING, BUTTERFLIES IN STOMACH] ```
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Skeletal reflexes
involve proprioceptors & somatic motor neurons spinal reflexes: • CNS integrates input signal • mono- or polysynaptic pathways • efferent neuron - somatic (alpha) motor neurons • effectors - skeletal (extrafusal) muscle fibers - mediated by Golgi tendon organ and muscle spindle organ
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Proprioceptors (skeletal muscle reflex)
• sensory receptors in skeletal muscle, joint capsules, & ligaments • sense body position & change non voluntary response, its a reflex
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Golgi tendon organ
monitors muscle force and mediates tendon reflex - regulates muscle force, - locates near the tendon • innervated by sensory neuron (Ib afferent) • mechanically-gated channels -> graded (receptor) potential
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Muscle spindle organ
monitors muscle length and mediates stretch reflex (patellar , knee jerk) - regulates muscle length - located within muscle fibers • innervated by sensory neuron (Ia afferent) • mechanically-gated channels -> graded (receptor) potential Postural control!!! Ex: patellar stretch reflex
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Golgi tendon reflex and muscle relaxation
this happens to prevent muscle damage, when there is too much force, the golgi relaxes the muscles. polysynaptic pathway • Ib afferent -> Ib inhibitory interneuron -> motor neuron
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Muscle tone
muscle spindles monitor muscle length