Pharmacology 1 Flashcards

1
Q

What is Pharmacology

A

Defined as the study of substances that interact with living systems thro chemical processes, especially by binding to regulatory molecules and activating or inhibiting normal body processes

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2
Q

What is a drug

A

Defined as a natural product, chemical substance, or pharmaceutical preparation intended for administration to a human or animal to diagnose or treat a disease

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3
Q

How does the body handle drugs

A

ADME

Absorption, distribution, metabolism, elimination

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4
Q

What are pharmacokinetics

A

how the body handles the drug

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5
Q

Bioavailability

A

The fraction of the administered drug that reaches the systemic circulation

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6
Q

Onset of Action

A

Time after administration at which you see the drug effect

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7
Q

duration of action

A

time during which plasma concentration stays above the MEC for desired effect

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8
Q

half-life

A

time required for plasma concentration of a dug to decrease by 1/2 after absorption and distribution are complete

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9
Q

Therapeutic Window

A

Where you want to effects to occur. it above the MEC for desired response and below the MEC for adverse response

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10
Q

Whats the MEC

A

Min effective concentration

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11
Q

What happens during distribution

A

After reaching the blood stream, drugs get distributed into various tissues in the body in two phases

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12
Q

Initial phase of distribution

A

Distribution to interstitial and intracellular space, and to highly perfused organs such as liver, kidney and brain

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13
Q

Second Phase of distribution

A

Distribution to muscles, most viscera, skin, bone and fat that is slower

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14
Q

What does drug metabolism (biotransformation) do

A

Enhances elimination of drugs by increasing their excretion, terminate the action of drugs and endogenous substance and activates certain prodrugs to their active form

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15
Q

Where are the sites of metabolsim

A

Mainly in the liver, kidneys play an important role in the metabolism of some drugs, a few are done in blood and intestinal wall

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16
Q

What are the two forms a drug can be in when excreted

A

it could be unchanged or it can be converted to metabolites

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17
Q

what kind of compounds do excretory organs expel best (lungs exuded)

A

Polar compounds are excreted much easier than substances with high lipid solubility

18
Q

What must happen to lipid soluble drugs to be eliminated

A

they must be metabolized to more polar compounds before they can be excreted

19
Q

What kind of drugs are excreted in feces

A

Unabsorbed oral drugs or drug metabolites excreted either in the bile or into the intestinal tract and are not reabsorbed

20
Q

Why is excretion of the lungs important

A

Mainly for the elimination of anesthetic gases and volatile compounds such as ethanol

21
Q

whats the most important organ for excreting drugs and their metabolites

A

the kidneys

22
Q

What is Pharmacodynamics

A

Study of what drugs do to the body. Drug effects, mec of action, measurement of drug action, modulation of drug action

23
Q

what are some common drug targets

A

receptors, enzymes, carrier molecules, voltage-gated ion channels

24
Q

What are receptors as drug targets

A

A structure on the surface of a cell (or inside a cell) that selectively received and binds a specific substance causing a change in cell function

25
Q

what are enzymes as drug tragets

A

usually macro-molecules proteins that act as a catalyst

26
Q

Carrier molecules a drug targets

A

transport a chemical across a membrane with in the body to allow it work

27
Q

Ion channels as drug targets

A

allow passage of ions across bio membrane and allow them to open and or close

28
Q

what is signal transuction

A

An extracellular signaling molecule (ligand or agonist) activates a receptor on the cell membrane and this receptor in turn activates intracellular ‘second messagers” that cause a response

29
Q

what is the dose in pharmacodynamics

A

the amount of drug administered

30
Q

what is response in pharmacodynamics

A

the effect

31
Q

what is the potency of a drug

A

The amount of drug needed to produce a given effect

the dose causing 50% of the max effect is the EC50

32
Q

what is efficacy

A

Efficacy (maximal efficacy) is the greatest effect (Emax) an agonist can produce if the dose is taken to very high levels

33
Q

What is an agonist

A

a molecule that binds to a receptor, producing a physiological or pharmacological reponse

34
Q

What is a partial agonist

A

A molecule that binds to a receptor, producing a less than full physiological or pharmacological response

35
Q

what is an antagonist (blocker)

A

A molecule that binds to a receptor and prevents the binding of an agonist and thus prevents or reduces the effect of agonist. an ideal antagonist does not produce any response by itself

36
Q

competitive Antagonist effect on DRC

A

shift the DR to the right, and does not affect the efficacy of the agonist until all receptors are occupied (parallel shift)

37
Q

Non-competitive antagonist effect on DRC

A

shifts it to the right, but also reduces the efficacy of the agonist (non-parallel shift)

38
Q

What are the effects of drugs classified under

A

Desirable (therapeutic) and undesirable

39
Q

What are the classifications of undesirable effects

A

Non-deleterious (side effects)

deleterious (toxic effects)

40
Q

What is an adverse drug event (ADV)

A

a reaction to a drug that is harmful or an unintended response (could be an allergy or organ toxicity)

41
Q

What is an ADR

A

adverse drug effect