4.2 physiology of GABA and Glycine Receptors Flashcards

1
Q

describe GABA C receptor

A

-ionotropic and activates a Cl- channel (let’s Cl- go into cell) -Only found in the retina.

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2
Q

which 2 receptor types don’t belong with the others? ACh, glutamate, GABA, glycine, ATP, serotonin receptors.

A
  1. ATP has its own Ligand-gated ion channel gene family 2. glutamate has its own gene Ligand-gated ion channel family 3. all the others share the same Ligand-gated ion channels gene superfamily
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3
Q

what’s the difference between GABA A/glycine receptors and ACh nicotinic receptors? Why do these receptors signal different effects (i.e. why do the channels have different ion selectivity)?

A

these receptors are similar but the amino acids lining the pore of the channel are different: 1. ACh: negatively charged. 2. GABA A/Glycine are + charged

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4
Q

name some compounds that activate GABA A. why do they have different effects ?

A
  1. general anesthetics, benzodiazepines (antianxiety agents and muscle relaxants), barbiturates and alcohol 2. There are different GABA(A) subtypes types and different agents can bind selectively to different subtypes
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5
Q

name 2 effects of the GABA found in interstitial fluid that constantly provides low-level activation of GABA A receptors

A

1.Cuts down on the noise in the brain. 2. Increases the signal-to-noise ratio in the brain.

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6
Q

is glycine excitatory?

A

it can be. 2. Glycine can bind to NMDA receptors and make them more sensitive to glutamate

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7
Q

where’s glycine found?

A

mainly found in the brainstem and spinal cord

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8
Q

glycine can also be inhibitory. how do we know this?

A

strychnine antagonizes glycine. Strychnine antagonizes the direct inhibition provided by glycine and leads to convulsions and muscular hyperactivity

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9
Q

how is glycine removed from synaptic cleft?

A

Glycine is taken back into the presynaptic terminal by a glycine transporter

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10
Q

what happens to ions in this EPSP?

A

They travel down their concentration gradient, depolarizing the cell

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11
Q

during IPSP, does the cell depolarize or hyperpolarize? which way does K+ go? Cl-?

A
  • K+ will leave cell
  • Cl- will enter cell

Effect is hyperpolarization

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12
Q
  1. define reversal potential.
  2. what is K+ reverse potential?
  3. when K+channels open, and K+ moves, is this more consitently stimulatory or inhibitory?
A
  1. “when you open a channel, the ion will flow to attempt to reach reversal potential”
  2. -80mv
  3. Opening K+ channels is more consistently inhibitory
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13
Q

what happens when GABA activates a Cl- receptor in a pt in early development? 3. How does trend change over time to rectify this problem?

A
  1. Early in development, Cl- is moved into the cell by a Na-K-Cl cotranporter
  2. now the [Cl-] is higher inside the cell -> when GABA receptor opens Cl- channel, the Cl- leaves the cell (opposite of adults)
  3. The K+/Cl- cotransporter is not expressed in early development (this pump wouldkeep Cl- out of the cell)
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14
Q

what are the 3 types of inhibitory synapses in the spinal cord?

A

–Ones that use GABA
–Ones that use glycine
–Ones that use both GABA and glycine

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