Physiology Study Guide

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178 Terms

1
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What is sensory transduction and why does it matter

It converts stimulus energy into receptor potentials so the nervous system can interpret the world

2
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How does receptor adaptation help survival

It reduces response to constant stimuli so novel signals stand out

3
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Why do mechanoreceptors need specialized structures

They shape stimulus filtering and sensitivity so only relevant forces trigger signals

4
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How would damage to cilia on a sensory pit affect detection

It would blunt mechanotransduction and reduce sensitivity to ripples and pressure

5
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Why does stimulus intensity encode as frequency not amplitude

Spike amplitude is fixed while higher intensity drives higher firing rates

6
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How do receptive fields influence acuity

Smaller fields and higher density allow finer spatial discrimination

7
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Why do lateral inhibition circuits increase contrast

Inhibitory interneurons suppress neighbors so edges appear sharper

8
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What tradeoff exists between sensitivity and specificity in receptors

High sensitivity risks false alarms while high specificity may miss weak signals

9
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How would cold water shift thermoreceptor activity

Cold receptors increase firing and warm receptors decrease firing to signal temperature drop

10
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Why does multimodal integration improve detection

Combining cues reduces ambiguity and noise so perception is more reliable

11
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How do hair cells convert motion into voltage changes

Stereocilia deflection gates ion channels and changes membrane potential

12
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Why does stimulus duration affect coding strategy

Phasic receptors signal change while tonic receptors signal persistence

13
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How would increased background noise in water affect ISO function

Signal to noise falls so the animal relies more on temporal patterns and integration

14
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Why do threshold and dynamic range both matter

Threshold sets detection limits and dynamic range preserves differences across intensities

15
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How does adaptation speed relate to stimulus statistics

Fast adaptation suits transient cues while slow adaptation suits sustained cues

16
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Why are labeled lines useful for the brain

Dedicated pathways preserve modality identity from periphery to cortex

17
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How would damage to the trigeminal branch alter perception

Facial mechanosensation and electroreception would be impaired

18
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Why does spatial summation help weak stimuli be detected

Multiple subthreshold inputs add to cross threshold for spiking

19
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How do temporal patterns encode stimulus features

Burst timing and interspike intervals carry information beyond rate

20
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Why are chemoreceptors vital in aquatic habitats

Chemical plumes carry prey and danger information when vision is limited

21
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How would an increase in water viscosity change mechanosensation

Ripple propagation changes and receptors may need closer range to detect movement

22
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Why is adaptation reversible in healthy receptors

Molecular mechanisms reset channels and synapses to baseline

23
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How do amplification mechanisms improve detection

Mechanical and electrical gain boosts small inputs into usable signals

24
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Why is receptor distribution across the body uneven

Functional hotspots concentrate sensors where they are most useful

25
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How does expectation modulate sensory gain

Top down input can increase or decrease sensitivity for task goals

26
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Why are slow and fast mechanoreceptors both needed

They extract complementary features of the same stimulus

27
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How would partial blockage of ion channels affect sensitivity

It raises threshold and narrows dynamic range

28
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Why does the nervous system need noise tolerance

Biological sensors are noisy and robust coding preserves key information

29
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How can redundancy improve reliability

Multiple sensors of the same type allow error correction

30
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Why are internal states able to change perception

Neuromodulators alter receptor and circuit gain to match context

31
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32
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How are the central and peripheral nervous systems divided by function

The PNS gathers and delivers signals while the CNS integrates and commands

33
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Why are glial cells essential and not passive

They support metabolism maintain ions modulate synapses and shape plasticity

34
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How does myelination speed conduction

It increases membrane resistance and enables saltatory conduction at nodes

35
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What determines conduction velocity in an axon

Axon diameter myelination and temperature set speed

36
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How would demyelination change reflexes

Conduction slows and temporal dispersion weakens synchronous activation

37
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Why do neurons have axon hillocks for spike initiation

Channel density and geometry create the lowest threshold region

38
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How does the Nernst potential define ionic driving force

It sets the equilibrium voltage so differences drive current when open

39
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Why is the resting membrane potential negative

Selective permeability to potassium and pumps create a negative interior

40
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How do voltage gated channels create action potentials

Rapid sodium activation followed by potassium activation makes a spike

41
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Why do refractory periods enforce directionality

Inactivated sodium channels prevent immediate reexcitation behind the wave

42
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How does divergence and convergence support computation

Divergence broadcasts signals and convergence enables integration

43
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Why are circuits organized into feedforward and feedback loops

Feedforward drives responses and feedback refines gain and stability

44
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How would increasing extracellular potassium affect excitability

Higher potassium depolarizes cells and may trigger spontaneous firing

45
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Why are sensory maps topographic

Ordered projections preserve spatial relationships for efficient processing

46
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How do spinal reflexes illustrate sensorimotor integration

Afferents synapse on motor neurons for rapid automatic responses

47
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Why does the autonomic system have dual divisions

Sympathetic and parasympathetic balance arousal and recovery

48
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How do neuromodulators reconfigure circuits

They change channel properties and synaptic efficacy to shift network state

49
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Why is energy supply crucial for neural coding

Spiking and pumping are ATP intensive so metabolism limits activity

50
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How would hypoxia affect neural function

Reduced ATP impairs pumps and transmission causing failure of coding

51
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Why do inhibitory neurons sharpen tuning

Inhibition sculpts timing and contrast to increase selectivity

52
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How do central pattern generators produce rhythmic behavior

Reciprocal inhibition and intrinsic currents yield oscillations

53
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Why are sensory afferents organized by modality and speed

Parallel pathways optimize timing and processing needs

54
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How does plasticity in development shape circuits

Activity dependent pruning and strengthening refine connectivity

55
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Why are the meninges and CSF important for function

They protect nourish and clear waste to preserve neural health

56
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How would increased intracranial pressure impact signaling

Axonal and synaptic function degrade due to compression and reduced perfusion

57
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Why do projection neurons and interneurons differ in roles

Projections carry information long distances while interneurons compute locally

58
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How does the blood brain barrier support stable signaling

It regulates entry of molecules and shields circuits from toxins

59
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Why are nodes of Ranvier spaced optimally

Spacing balances speed energy cost and reliability

60
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How would temperature drops influence speed

Cooler temperatures slow kinetics and reduce conduction velocity

61
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Why does redundancy appear in parallel pathways

It adds robustness and allows specialization for context

62
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63
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How do graded potentials differ from action potentials in function

Graded signals are analog and local while spikes are digital and long range

64
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Why is the synapse often the limiting step for speed

Neurotransmitter release and diffusion add delay compared with conduction

65
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How does calcium trigger vesicle release at synapses

Calcium binds sensors and drives vesicle fusion with the membrane

66
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Why do SNARE proteins matter for transmission

They assemble the fusion machinery that releases transmitter

67
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How would lowering extracellular calcium affect synaptic strength

Release probability falls and EPSPs weaken

68
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Why does temporal summation depend on membrane time constant

Longer time constants allow EPSPs to overlap and add

69
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How do spatial and temporal summation enable decisions

Multiple inputs integrate to reach threshold or fail

70
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Why is inhibition not just the opposite of excitation

It controls timing gain and subthreshold dynamics to shape codes

71
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How do metabotropic receptors alter network state

They change intracellular cascades and modulate channels for seconds

72
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Why does short term plasticity encode recent history

Facilitation and depression adjust strength based on prior activity

73
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How would synaptic depression influence sensory adaptation

Prolonged input weakens synapses and reduces response

74
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Why does long term potentiation support learning

Hebbian pairing strengthens synapses to store associations

75
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How does spike timing dependent plasticity add precision

Relative timing of spikes sets direction and magnitude of change

76
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Why are axo axonic synapses powerful for control

They modulate release probability without changing postsynaptic gain

77
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How do electrical synapses aid synchrony

Gap junctions pass current directly to align timing

78
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Why would shunting inhibition change integration without big IPSPs

It increases conductance and reduces EPSP amplitude by division

79
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How do neuromodulators bias plasticity rules

They gate kinase pathways and set whether potentiation or depression occurs

80
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Why does dendritic location of synapses matter

Distance and branch properties shape local boosting and attenuation

81
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How do backpropagating action potentials inform learning

They signal dendrites about outputs and enable coincidence detection

82
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Why does receptor desensitization protect circuits

It limits overstimulation and preserves dynamic range

83
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How would antagonists at receptors alter computation

They block channels or cascades and reweight circuit balance

84
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Why do synapses use release probability rather than fixed output

Stochastic release supports flexibility and encoding of uncertainty

85
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How does synaptic pruning improve efficiency

It removes weak or redundant connections to streamline processing

86
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Why is homeostatic plasticity necessary

It stabilizes activity around set points despite perturbations

87
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How do inhibitory plasticity rules support balance

They tune inhibition to track excitation and prevent runaway firing

88
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Why are neuromodulatory systems good drug targets

Small changes can reconfigure large scale network dynamics

89
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How would chronic stress alter synaptic function

It changes receptor expression and dendritic structure reducing plasticity

90
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Why is coincidence detection central in sensory brain areas

Precise timing links features into coherent percepts

91
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How do ensemble level dynamics emerge from synapses

Population interactions create oscillations and codes richer than single neurons

92
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93
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What is a circadian rhythm and why is it adaptive

It is a near 24 hour cycle that anticipates daily changes to optimize physiology

94
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How does the SCN coordinate body clocks

It synchronizes peripheral oscillators via neural and hormonal signals

95
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Why are zeitgebers important for alignment

External cues like light and feeding reset internal clocks to local time

96
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How would constant dim light affect rhythms

Amplitude falls and phase drifts leading to internal desynchrony

97
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Why does melatonin signal darkness not sleep

It conveys night timing and modulates systems that enable sleep propensity

98
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How do clock genes create oscillations

Feedback loops of transcription and translation generate stable cycles

99
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Why are peripheral clocks necessary

Local tissues time metabolism and function to their specific demands

100
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How would night feeding shift liver clocks

Feeding time resets hepatic rhythms and may misalign with the SCN