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Goodman and Gilmans The Pharmacological Basis of Therapeutics 13th Edition Brunton

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Goodman and Gilmans The Pharmacological Basis of Therapeutics 13th Edition Brunton

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  • August 17, 2024
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Test Bank For Goodman and Gilmans The Pharmacological
Basis of Therapeutics 13th Edition Brunton | 9781259584732 |
All Chapters with Answers and Rationals

What is clinical pharmacology? - ANSWER: The study of drug action in man, providing the scientific
basis for rational, safe and effective prescribing

What is pharmacodynamics? - ANSWER: The study of what the drug does to the body

What are drug receptors? - ANSWER: They are proteins or glycoproteins that are either on the cell
surface, or on an organelle within the cell, or in the cytoplasm.

Name some common types of receptor. - ANSWER: - Channel-linked
- GPCRs
- Enzyme-linked
- Nuclear receptors

Describe the drug-dose response curve. - ANSWER: Curve which illustrates a drug dose and its efficacy
through measures of Emax and ED50.

What does Emax represent? - ANSWER: The maximal response of a drug

What does ED50 represent? - ANSWER: The level at which 50% of population has therapeutic effects

Define therapeutic index - ANSWER: The ratio between the toxic dose and the therapeutic dose of a
drug, used as a measure of the relative safety of the drug for a particular treatment.

What is suggested by a large therapeutic window? - ANSWER: A drug with good beneficial effects and
low risk of adverse effects

What is an agonist drug? - ANSWER: A drug or substance that binds to a receptor inside a cell or on its
surface and causes the same action as the substance that normally binds to the receptor.

What is an antagonist drug? - ANSWER: A drug that blocks the receptor so they can't be activated by
the substance that would normally bind it.

What effect will an antagonist have on a drug-dose response curve? - ANSWER: Pushes the curve right

Define drug efficacy. - ANSWER: The extent to which a drug can have its effect.

Define drug potency. - ANSWER: The ability of a drug to achieve its effect at lower doses.

What is drug selectivity? - ANSWER: Ability of drug to interact with specific receptors of target tissue
and not with other receptors

What is drug desensitisation? - ANSWER: The reduced sensitivity of a receptor to a drug after a period
of time.

Define tachyphylaxis - ANSWER: Rapid decrease in response to the drug - "acute tolerance"

What are some of the causes of drug desensitisation? - ANSWER: 1. Receptor down-regulation:
reduction in the number of receptors
2. Changes in receptor structure or function

, 3. Exhaustion of mediators e.g. G-proteins
4. Physiological adaptation

What are some of the causes of reduced drug response? - ANSWER: 1. Altered physiology (weight,
age)
2. Disease progression
3. Drug interactions (e.g. starting a new drug)
4. Reduced adherence to regime

What is pharmacokinetics? - ANSWER: What the body does to the drug

What are the 4 phases of pharmacokinetics? - ANSWER: ADME

Absorption
Distribution
Metabolism
Excretion

How are drugs absorbed? - ANSWER: Various different routes, depending on administration:

Oral, buccal, sublingual, rectal, IV, IM, SC, inhalation, transdermal, topical

What is the importance of route of administration on absorption? - ANSWER: Influences the rate of
absorption, also overcomes physiological issues e.g. first pass metabolism

What is the bioavailability of a drug? - ANSWER: Percentage of drug absorbed into systemic
circulation

Describe first-pass metabolism. - ANSWER: When the concentration of a drug is reduced before
systemic circulation, due enzymes in the intestinal wall and liver.

Which system in the liver accounts for most of the first-pass metabolism of drugs (hepatic
extraction)? - ANSWER: Cytochrome P450 (CYP450)

Which GI routes of administration may be utilised to overcome first-pass metabolism? - ANSWER:
Buccal, sublingual and rectal

How are buccal and sublingual drugs absorbed? - ANSWER: Into the capillaries of the oral circulation -
> drained into the vena cava -> returned to the heart -> pumped into systemic circulation

How are rectal drugs absorbed? - ANSWER: Lower 2/3s drained by inferior and middle haemorrhoidal
veins -> vena cava -> heart -> system circulation

What is the most direct route of drug administration into the systemic circulation? - ANSWER:
Intravenous (IV)

Ideal for very ill patients where a rapid response is required

In which case is it preferable to give an IV infusion over an injection? - ANSWER: When a drug has a
low therapeutic index, as high drug concentration in the plasma may not be desirable

In a drug concentration-time curve, what does a smaller area under curve (AUC) indicate? - ANSWER:
Reduced bioavailability

Usually seen in orally administrated drugs when compared to IV.

What are the 3 major compartments that a drug may be distributed into? - ANSWER: 1. Plasma

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