Exam 2 lecture 12 Flashcards

1
Q

Pharmacokinetics alcohol

A

Administration: orally (very high concentration)

Metabolism: 95% alcohol dehydrogenase (in intestines, stomach, liver), 5% cytochrome P450

Elimination: Urine and breathing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Pharmacodynamics alcohol

A

-GABAa receptor modulator
-NMDA receptor antagonist (learning and memory)
-L-type voltage-gated Ca2+ channel inhibited
-Agonist for endocannabinoid receptors (reward/happy)
-Intracellular pathways

-Slows down/inhibits all brain function

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Pharmacokinetic tolerance

A

-Drinking increases, enzymes increase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Regular pharmacodynamic tolerance

A

-Fewer receptors made

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Acute pharmacodynamic tolerance

A

-More drunk at the beginning of drinking than end

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Opoids

A

-Great pain medication
-Incredibly addictive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Opioid drugs

A

-Morphine, heroine, fentanyl

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Pharmacodynamics opioids

A

-All receptors metabotropic and inhibitory (reduced firing rates)

-Delta
-Kappa
-Mu
-Nociception

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Sensory systems

A

Opioids make sensory systems less sensative

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Pharmacokinetics opioids

A

-Absorption: Oral (slow), intravenous (fast, good high, addictive)

Metabolism: Cytochrome p450

How well did you know this?
1
Not at all
2
3
4
5
Perfectly