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NUR 751 Pharmacology Basics and Cell Physiology–Questions and Answers | 2026 Update | 100% Correct

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NUR 751 Pharmacology Basics and Cell Physiology–Questions and Answers | 2026 Update | 100% Correct

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NUR 751 Pharmacology Basics and Cell
Physiology–Questions and Answers | 2026 Update |
100% Correct.
Receptor Theory

-Concept where ligand binding activates or deactivates receptors

- effect is produced by ligand binding

-effect is absent when not bound by ligand

Agonist

Binds to and activates a receptor

Antagonist

Binds to a receptor without activating it

Competitive antagonism

Increasing antagonist concentration inhibits agonist response

Noncompetitive antagonism

-Antagonist prevents receptor activation despite high agonist concentration

-covalent bonding

-allosteric inhibition

Partial agonists/agonist-antagonists

-Activate receptors less completely than full agonists

-can reduce agonist effects

,Allosteric inhibition

Inhibition of receptor function by binding at a site other than the active site

Hypersensitive

Exhibiting an exaggerated/inappropriate response to drug in sensitized individual

Hyporeactive

Exhibiting a diminished response to stimuli

Tolerance

Decreased response to a drug following repeated exposure

Tachyphylaxis

Rapid development of tolerance to a drug

Additive effect

Combined effect of two drugs equals the sum of their individual effects

Synergistic effect

Combined effect of two drugs is greater than the sum of their individual effects

Distribution

Movement of drugs within the body

Hepatic Clearance

R = Q(Cin-Cout)

Where:

, R = rate of clearance

Q = Liver blood flow

Cin = Concentration flowing into the liver

Cout = Concentration flowing out of the liver

If the liver could completely extract the drug from afferent flow, clearance would equal liver

blood flow.

Volume of Distribution

-Theoretical volume drugs would occupy in the body

-highly lipid soluble drugs have large calculated Vd

Enantiomers

Mirror image molecules with different pharmacokinetic and pharmacodynamic properties

Pharmacodynamic variability

Variability in drug response due to differences in enzyme activity and genetics

Pharmacokinetic Variability

Bioavailability

Renal function

Hepatic function

Cardiac function

Patient age

Extracellular Fluid

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