Neuropharmacology Continued Flashcards

1
Q

drugs may block synthesis enzymes, axonal transport of raw materials, or the ability to store transmitter

A

Transmitter Production

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2
Q

drugs can block action potentials by blocking ion channels

A

Transmitter Release

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3
Q

can be affected by drugs

A

Autoreceptors

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4
Q

a drug may block reuptake of transmitter or block enzymes

A

Transmitter Clearance

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5
Q
  • Receptor antagonists block postsynaptic receptors from being activated
  • Receptor agonists bind to receptors and activate them
A

Drugs Can Affect Transmitter Receptors

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6
Q
  • Receptor up or down regulation
  • Activation of second messenger systems
  • Activation of genes
A

Drugs Can Alter Intracellular Postsynaptic Processes

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7
Q

can relieve severe symptoms of schizophrenia

A

Psychoactive Drugs

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8
Q

a class of drugs that alleviate symptoms of schizophrenia, typically by blocking dopamine D2 receptors

  • Examples: thorazine, haldol
A

First-Generation Antipsychotics (neuroleptics)

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9
Q

act on receptors in addition to, or other than, D2 receptors, and may relieve symptoms resistant to typical antipsychotics

  • Examples: clozaril, seroquel
A

Second-Generation Antipsychotics

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10
Q

are used to treat disturbances of mood called affective disorders

  • → accumulation of transmitters, prolonging their activity, is a major feature
A

Antidepressant Drugs

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11
Q

prevent the breakdown of monoamines at the synapses

A

Monoamine Oxidase Inhibitors (MAOIs)

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12
Q

act specifically at serotonergic synapses (e.g., prozac, celexa)

A

Selective Serotonin Reuptake Inhibitors (SSRIs)

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13
Q

block reuptake of serotonin and norepinephrine and may be used with treatment-resistant depression

A

Tricyclic Antidepressants

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14
Q

are drugs that reduce nervous system activity

A

Depressants

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15
Q

are older anxiolytic drugs and sleep aids that depress (or reduce) nervous system activity

  • They are addictive and easy to overdose on (e.g., phenobarbital)
A

Barbiturates

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16
Q

act as agonists on GABA_A receptors and enhance the inhibitory effects of GABA

A

benzodiazepines