lecture1and2 Flashcards

1
Q

what is pharmacology

A

is the biomedical science concerned with the interaction of chemical substances with living cells tissue and organisms

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

what is pharmacokinetics

A

a division of pharmacology focused on processes that affect drug concentration in the body what the body does to the drug.

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

What is pharmacodynamics

A

a division of pharmacology focused on how a drug produces an effect what the drug does to the body

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

what is toxicology

A

is the science of poisons and toxicity, it focuses on the harmful effects of drugs.

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

what is pharmacy

A

the science and profession concerned with the preparation, storage, dispensing, and proper, utilization of drug products

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

what is the difference between a prescription and non-prescription medication

A

prescription medication, drugs whose sale is restricted and available only with a prescription from a licensed provider, whereas a nonprescription medication or OTC drugs can be sold with direction for safe use by the public.

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

what are the steps to bring a new drug to the market

A

identification of the compound, invitro experimentation on animals, clinical testing…Phase 1 small number of patients tests are dosing range in typically healthy volunteers is it safe 20-100 subjects?, phase 2 testing the drug with a relatively small number of patients 100-200 to determine if drug actually works or has desired effects, Phase 3 similar to phase 2 but larger number of patients 1000-6000 with stats applied and with controls Phasedoes it work with a double blind study? 4 continual monitoring of the drug during clinical use.

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

what is the abuse potential scale

A

Schedule 1 is high abuse potential with little use like heroin no one can prescribe schedule 1, down to five small abuse potential.

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

how long does it take for a drug to come to market

A

8-9 years to go from identification of a compound to marketing and new drug application.

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

why is the generic name important

A

it is the name that will never change can be named for a number of reasons this is what we need to know.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the trade name

A

the name given to the product by the company that made it making someone a lot of money.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is the reference point for drug concetration in the body

A

the concentration in the blood.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what are the 5 categories of receptors

A

intracellular, intrinsic enzymatic activity, directly associate with intracellular enzymes, ligand gated ion channel, 7 membrane spanning receptors.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

tell me about intracellular receptors

A

usually lipophilic, for example estrogen vitamin A directly regulates gene activity usually slower response.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

tell me about intrinsic enzymatic activity

A

epidermal growth factor receptor, insulin receptor, TGF-betaR, protein phosphoralation common causing a cascade effect.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

tell me about ligand gated ion channels

A

like the nicotinic acetylcholine receptor, when activated opens a channel for something else.

17
Q

tell me about receptors that directly associate with intracellular enzymes

A

Interlueking-3 receptor erythropoeitin receptor leptin, attach to to a enzyme that can then produce the cascade effect.

18
Q

tell me about 7 transmembrane receptors

A

G protein coupled receptors, heptahelical, serpentine, cross membrane seven times and then can induce signaling

19
Q

what is down-regulation or up-regulation

A

continual stimulation will lead to a decease in the receptor numbers, continued exposure to an inhibit will lead to an increase in the receptor number.

20
Q

what is the dissociation constant

A

Kd=[R][L]/[RL] so the more drug I add the more it will bind to the receptor. Receptors bound to ligand.

21
Q

what is Kd

A

when the number of bound receptors = the number of free ligands and receptors,

22
Q

when looking at the curves of binding affinity which side has the highest binding affinity

A

the one on the lowest concentration to occupy half the receptors, usually on the left.

23
Q

what is the Ec50

A

the effective concentration that will produce a half maximal effect

24
Q

what is potency

A

a measurement of drug dose used to compare the relative affinity and effectiveness of two or more drugs. This is the most conveniently done by comparing EC50 of two or more agents. The further to the left on the potency curve

25
Q

what is efficacy

A

the maximal effect a drug can induce Emax

26
Q

what is an agonist

A

a drug or ligand that binds to a receptor and produces a molecular, cellular, or physiological response.

27
Q

what is an antagonist

A

a drug that inhibits the response of the agonist

28
Q

what is a competitive antagonist

A

binds to the same site as the agonist blocking it, so shifts the EC50 to the right but does not effect the maximal effect of the drug.

29
Q

what is a noncompetitive antagonist

A

binds at a different site than the agonist. Will decrease the maximal effect. Emax. Does not matter how much agonist is present it will knock out the receptor almost like it reduces the number of receptors.