Pharmacology 1 Flashcards

(41 cards)

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

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
what are enzymes as drug tragets
usually macro-molecules proteins that act as a catalyst
26
Carrier molecules a drug targets
transport a chemical across a membrane with in the body to allow it work
27
Ion channels as drug targets
allow passage of ions across bio membrane and allow them to open and or close
28
what is signal transuction
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
what is the dose in pharmacodynamics
the amount of drug administered
30
what is response in pharmacodynamics
the effect
31
what is the potency of a drug
The amount of drug needed to produce a given effect | the dose causing 50% of the max effect is the EC50
32
what is efficacy
Efficacy (maximal efficacy) is the greatest effect (Emax) an agonist can produce if the dose is taken to very high levels
33
What is an agonist
a molecule that binds to a receptor, producing a physiological or pharmacological reponse
34
What is a partial agonist
A molecule that binds to a receptor, producing a less than full physiological or pharmacological response
35
what is an antagonist (blocker)
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
competitive Antagonist effect on DRC
shift the DR to the right, and does not affect the efficacy of the agonist until all receptors are occupied (parallel shift)
37
Non-competitive antagonist effect on DRC
shifts it to the right, but also reduces the efficacy of the agonist (non-parallel shift)
38
What are the effects of drugs classified under
Desirable (therapeutic) and undesirable
39
What are the classifications of undesirable effects
Non-deleterious (side effects) | deleterious (toxic effects)
40
What is an adverse drug event (ADV)
a reaction to a drug that is harmful or an unintended response (could be an allergy or organ toxicity)
41
What is an ADR
adverse drug effect