Psychopharmacology Flashcards

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1
Q

Psychopharmacology

A

A field interested in studying the effects of drugs on the nervous system and behaviors

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2
Q

Drug

A

an exogenous chemical not necessary for normal cellular function that significantly alters the functions of the certain cells of the body when taken in relatively low doses

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3
Q

pharmacokinetics

A

studies how drugs move through the entire body and process the chemicals

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4
Q

Pharmacodynamics

A

studies how drugs change the body

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5
Q

What does pharmacodynamics cover?

A

Absorption, distribution, metabolism, and excretion

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6
Q

oral administration

A

most common, broken down by stomach acid, some drugs destroyed this way (insulin)

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7
Q

Sublingual administration

A

placed under tongue and dissolved, absorbed by capillaries that supply mucous membrane of mouth

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8
Q

intrarectal administration

A

into rectum, most common for drugs that upset the stomach

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9
Q

inhalation

A

vaporous substance into lungs; route from lungs to brain is short, so drugs have rapid effects

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10
Q

Topical administration

A

directly onto skin or through mucous membrane of nose

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11
Q

Subcutaneous injections

A

into space beneath skin, useful if small amount is needed

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12
Q

IV

A

directly into vein, fastest route. entire dose releases into bloodstream instantly.

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13
Q

Intraparietal injection

A

into the parietal cavity

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14
Q

Intramuscular injection

A

directly into a muscle

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15
Q

intracerebral injection

A

injected directly into brain. used when the med cant cross the BBB

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16
Q

Intracellular ventricular injection

A

into one of the cerebral ventricles; widespread distribution of a drug throughout brain.

17
Q

What is the speed of absorption based on?

A

The route of administration and lipid solubility

18
Q

Where are most drug cites of action located?

A

the central nervous system

19
Q

Enzymes

A

deactivate drugs. proteins that act as a catalyst to accelerate chemical reactions, found primarily in the liver

20
Q

what does pharmacodynamics cover?

A

drug effectiveness, reuptake or destruction of NT’s, production, storage, and ligand and receptor binding

21
Q

Dose response curves

A

a graph of the magnitude of the drug effect based on the amount of the drug

22
Q

Why does drug effectiveness vary?

A

drugs vary in their affinity, with their sites of action. placebo effect , repeated administration

23
Q

Drug affinity

A

the extent to which a drug binds to receptors

24
Q

Placebo

A

an innocuous substance with no specific effect

25
Q

Nocebo

A

negative expectations lead to a negative outcome

26
Q

Tolerance

A

decreases the effectiveness of the drug

27
Q

sensitization

A

increases the effectiveness of the drug

28
Q

compensatory mechanisms

A

decrease in the effectiveness of binding to receptors. (reduced affinity or fewer receptors) A process that couples the receptors to ion channels in the membrane or to the production of second messengers (the second messengers become less effective)

29
Q

Agonists

A

facilitate postsynaptic effects

30
Q

Antagonists

A

block or inhibit postsynaptic effects

31
Q

The agonistic effect

A

binds with proteins and directly triggers the release of a NT (increases

32
Q

The antagonistic effect

A

The drug blocks the transporter molecules from filling the synaptic vesicles. The vesicles remain empty and nothing is released. This prevents the release of a NT

33
Q

A direct agonist

A

the drug mimics the effects of a neurotransmitter

34
Q

A direct antagonist

A

the drug binds with the postsynaptic receptor, but does not open the ion channel

35
Q

An indirect agonist

A

facilitates the opening of an ion channel

36
Q

An indirect antagonist

A

prevents the ion channel from opening

37
Q

Noncompetitive binding site

A

The drug binds to one site, but still allows another NT to bind to another site