Neuronal Ionic Currents Flashcards

different current types based on the ion channel

1
Q

Transient; rapidly activating and inactivating; current has large amplitude
Fxn: Generates APs

A

Na+

INa or INA,t

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2
Q

Persistent; rapidly activated by depolarizations like synaptic potentials but most importantly non-inactivating; current has smaller amplitude
Fxn: Enhances Depolarization from Excitatory inputs - may result in Plateau Potentials; contributes to steady-state firing

This current’s amplitude and cellular distribution has an important role in determining the responsiveness of neurons - it contributes to the baseline firing rate of neurons (pacemaker activity).

A

Na+

INA,p

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3
Q

Transient; rapidly inactivating; threshold for activation around -65mV (below standard AP threshold)
Fxn: generates rhythmic burst firing of APs

Through activation & inactivation of this current, neurons can generate slow Ca2+ spikes, which result in the generation of a high-frequency “burst” of short-duration Na+/K+ APs - because of their prolonged duration. Ex: thalamic relay neurons.

A

Ca2+

IT, low threshold

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4
Q

Long-lasting current; slowly inactivating; high-threshold for activation, around -20mV
Fxn: Underlies Ca2+ spikes that are prominent in dendrites; involved in synaptic transmission

High-voltage Activated (HVA); blocked by dihydropyridines (its antagonist)

A

Ca2+

IL, high threshold

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5
Q

Neither; rapidly inactivating; threshold around -20mV; modulated by a variety of neurotransmitters
Fxn: Underlies Ca2+ spikes that are prominent in dendrites; involved in synaptic transmission

High-voltage Activated; not blocked by dihydropyridines; blocked by conotoxin-GVIA; involved in the Ca2+ dependent release of neurotransmitters in the presynaptic terminals of some cell types.

A

Ca2+

IN

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6
Q

Purkinje; threshold around -50mV; these channels do not inactivate
Fxn: Generate Ca2+ spikes that are prominent in dendrites, strongly modulates firing pattern of neuron

High-Voltage Activated (HVA); not blocked by either dihydropyridines or conotoxin-GVIA; blocked by Agatoxin-BIA

A

Ca2+

IP

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7
Q

Activated by strong depolarization positive to -40mV; slow inactivation
Fxn: repolarization of APs and subsequent hyperpolarization

“Delayed-rectifier” bc the activation kinetics are slower than the transient Na current and therefore appear delayed.

A

K+

IK

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8
Q

Activated by increases in [Ca2+]i; rapid inactivation once membrane is repolarized
Fxn: AP repolarization and interspike interval

Calcium-Activated Potassium Current (1 of 2); voltage-dependent; controls freq. of AP generation during a steady depolarization by causing a marked hyperpolarization after the occurrence of each spike; contributes significantly to short spike intervals, due to its short time course.

A

K+

IC

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9
Q

Slow afterhyperpolarization; sensitive to increases in [Ca2+]i
Fxn: Slow adaptation of action potential discharge; the block of this current by neuromodulators enhances neuronal excitability

Calcium-Activated Potassium Current (1 of 2); not very voltage-dependent; slower in time course than IC; influences membrane potential mainly after a number of APs as a prolonged afterhyperpolarization; contributes significantly to the tendency of the firing freq. of some types of neurons to decrease during maintained depolarizations (spike freq. adaptation).

A

K+

IAHP

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10
Q

Transient; rapidly inactivating
Fxn: delayed onset of firing; lengthens interspike interval; AP repolarization

“Transient Potassium Current”; serves to delay the onset of the first AP; can also slow a neuron’s firing freq during maintained depolarization

A

K+

IA

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11
Q

muscarine sensitive; activated by depolarization of membrane to approx -65mV; non-inactivating
Fxn: contributes to spike frequency adaptation; the block of this current by neuromodulators enhances neuronal excitability

“Muscarine-sensitive Potassium currents”; blocked by stimulation of muscarine cholinergic receptors

A

K+

IM

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12
Q

Depolarizing (mixed cation) current that is activated by hyperpolarization
Fxn: contributes to rhythmic burst firing and other rhythmic activities

“Currents activated by hyperpolarization”; subsequently brings membrane potential back towards rest; the current in this family are carried by both Na and K ions; relatively slow in time course; activation results in slow depolarization of the cell, which generates a “pacemaker” potential that can activate repetitive Na and/or Ca2+ spikes.

A

K+

Ih

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13
Q

contributes to neuronal resting membrane potential

Fxn: the block of this current by neuromodulators can result in a sustained change in membrane potential

A

K+

IK,leak

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