Chapter 10 Flashcards

Introduction into pharm

1
Q

Deffinion of Pharmacodynamics

A

as medication is administered, it begins to alter a function or process within the body. simply put by binding to a regulatory molecules (proteins) and activating (turning on) or inhibiting (turning off) normal body process.

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

What is classified as a drug?

A

a drug is ANY substance that interacts with a molecule or protein that plays a regulatory role in living systems. Drugs MUST have a SPECIFIC size, charge, and shape to interact with a given receptor.

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

What is a receptor?

A

A receptor is a specific molecule, usually a protein, that interacts with a specific chemical in regulatory function. Receptors are responsible for the selectivity of drug action.

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

Endogenous

A

A substance made inside the body. endo, meaning inside, genous meaning from the beginning

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

Exogenous

A

A substances made outside the body. Exo, meaning outside the body.

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

What are hormones?

A

hormones are endogenous drugs made naturally inside the body.

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

Alpha (a)-1 Receptors

A

causes vasoconstriction of arteries and veins. Agonist Effect

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

Alpha (a)-2 Receptors

A

insulin restriction, glucagon secretion, inhibition of norepinephrine. Agonist Effect

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

Beta (b)-1 Receptors

A

increases heart rate, increases myocardial contractility, increases myocardial conduction, and renin secretion for urinary retention. Agonist Effect

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

Beta (b)-2 Receptors

A

Bronchus and Bronchiole reaction, insulin secretion, uterine relaxation, arterial dilation in certain key organs. Agonist Effect

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

Dapaminergic Receptors

A

vasodilation of renal and mesenteric arteries. Agonist Effect

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

Nicotinic Receptors

A

present at neuromuscular junction, allowing acetylcholine (ACh) to stimulate muscle contractions. Agonist effect

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

Muscarinic -2 Receptors

A

present in the heart; activated by ACh to effect sympathetic stimulation, decreasing heart rate, contractility, and electrical conduction velocity. Agonist Effect

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

Agonist Receptors

A

Is ANY drug that binds to a receptor and activates (starts) the receptor. in many receptors agonist leaving the binding site deactivated the receptor. however, in other agonist receptors, can permanently activates the receptors. Aspirin is an example.

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

Antagonist Receptors

A

Is ANY drug that binds to a receptor and PREVENTS (stops) the activation of the receptors.

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

Competitive Antagonist Receptors

A

Is ANY pharmacological Antagnoist that “competes” with the binding of against at the binding site.

17
Q

Noncompetitive Antagonist Receptors

A

Is ANY pharmacological antagonist that binds to a site on the receptor OTHER THAN the agonist binding site. it deactivate the receptors

18
Q

Physiologic Antagonist Receptors

A

When there is an EXCESS Histamine released by the body is a problem. Epinephrine is given to COUNTERACT the effect of the histamine

19
Q

Drug Receptor Interactions

A

Drugs interact with receptors by means of chemical forces or bonds: Covalent (permanently changing the receptors), Electrostatic (positives connecting to negatives), Hydrogen (hydro to nitro, or hydro to oxygen), lipophilic.

20
Q

Meaning of Affinity

A

How tightly the receptors binds to the drug

21
Q

Meaning of Bioavailability

A

Describes the concentration of drug in systemic blood in relation to amount of drug given.

22
Q

IV Bioavailability

A

100% bioavailability, because it is given directly into the blood.

23
Q

PO Bioavailability

A

ranges 10%-50% bioavailability, because blood from the GI tract goes directly to the liver. where first pass metabolism takes place.

24
Q

First Pass Effect

A

all drugs absorbed by GI tract enter the portal blood supply, and go directly to the liver. the liver metabolites many drugs before the enter the systemic blood supply.

25
Q

Potency

A

Potency: refers to the concentration of a drug needed for the effect. the less the concentration required, the more Potent the drug.

26
Q

Efficacy

A

Efficacy: refers to the effect of a drug. the more effect, the more efficacious the drug.