pharmodynamics Flashcards

1
Q

What is the study of pharmodynamics ?

A

The study of the biochemical and physiologic effects of drugs and the molecular mechanisms by which those effects are produced
( What drugs to do the body and how they do it )

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2
Q

what is the dose response relationship ?

A

Relationship between the size of an administered dose and the intensity of the response produced

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3
Q

what does the dose response relationship determine ?

A

The minimum amount of drug to be used
The maximum response a drug can elicit
How much to increase the dosage to produce the desired increase in response

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4
Q

a dose response curve will show ?

A

the maximal efficacy and the relative potency

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5
Q

what is maximal efficacy ?

A

known as the largest effect a drug can produce ( height of curve)

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6
Q

what is relative potency?

A

The amount of drug that must be given in order to elicit a response Can be important if a lack of potency forces inconveniently large doses and implies nothing about the maximal efficacy

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7
Q

Drugs are?

A

Chemicals that produce effects by interacting with other chemicals

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8
Q

receptors are ?

A

Special chemicals in the body that most drugs interact with to produce effects

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9
Q

true or false, when a drug binds to a receptor, it is usually reversible

A

True

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10
Q

receptor activity is usually regulated by what ?

A

Endogenous compounds

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11
Q

what happens when a drug binds to a receptor ?

A

it will either mimic or block the action of endogenous regulatory molecule and either increase or decrease the physiological activity controlled by that receptor

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12
Q

receptors can be classifed as?

A

Normal points of control of physiological processes

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13
Q

under normal physiologic conditions, receptors function is regulated by ?

A

molecules that have been supplied by the body

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14
Q

drugs produce therapeutic effects by :

A

by helping the body use its preexisting capabilities

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15
Q

true or false, drugs can both block and mimic the bodies own regulatory molecules

A

True

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16
Q

what are the 4 primary receptor families ?

A

Cell membrane–embedded enzymes
Ligand-gated ion channels
G protein–coupled receptor systems
Transcription factors

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17
Q

True or false The more selective a drug is, the greater the side effects there will be

A

False, the more selective a drug is , FEWER the side effects there will be

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18
Q

receptors and drug selectivity rely on what kind of mechanism ?

A

A lock and Key mechanism ( does not however gurentee safety)

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19
Q

What is the simple occupancy theory ?

A

the intensity of response to a drug is proportional to the number of receptors occupied

20
Q

maximal response is achieved with a drug when

A

When there is 100% receptor occupancy

21
Q

What is affinity ?

A

means the strength of the attraction - a high affinity means they are very potent

22
Q

what is intrinsic activity ?

A

ability for drug to activate receptor upon binding - higher intrinsic activity of a drug will mean there will be a more intense response seen in the maximal efficacy

23
Q

what is an agonist ?

A

drug binds to receptor- there is a response

24
Q

what is an antagonist ?

A

drug binds to receptor, there will be the blockage of a physiological response

25
what are non competitive antagonists ?
drug combines with multiple parts of the receptor and inactivates it
26
what are competitive agonists ?
27
what are partial agonists ?
drug binds to receptor, there is a diminished response
28
The number of receptors on the cell surface and the sensitivity to agonists can change in response to
continuous activation, down regulation, Desensitized or refractory
29
continuous inhibition of receptors will cause
hypersensitivty
30
what drug responses do not involve receptors ?
Simple physical or chemical interactions with other small molecules
31
name some kinds of drugs that dont use receptors
Antacids Antiseptics saline laxatives chelating agents
32
what is the ED 50?
Measurement of interpatient variability , the dose produces an effect in 50 % of patients
33
what are some clinical implications of interpatient variability
The initial dose of a drug is necessarily an approximation ED50 in a patient may need to be increased or decreased after the patient response is evaluated
34
what is the therapeutic index ?
ratio between LD50 which is the average lethal dose to 50% of animals tested with its ED50
35
The higher the therapeutic index means ?
The safer the drug
36
Age of a neonate ?
birth- 1 month
37
age of an infant ?
1-12 months
38
Age of a child
1- 12 years old
39
at what stage can a drug most easily pass through the placenta ?
during the last trimester ( blood flow to the fetus is the highest, increased surface area and increased amount of free drug circulating
40
drug induced development is at its greatest risk when ?
During the first trimester, due to the proliferation of cells and the fast development of organs
41
low serum creatinine is a indicator of?
poor kidney function
42
when there is a decline in renal functioning what happens ?
metabolism, declined cardiac output, delayed drug excretion, and possible drug accumulation because of this
43
why are hydrophiliic drugs a problem with older adults
they have less body water overall so the drug concentration could be higher for them
44
What are some characteristics of peds pts that will impact drug dosage?
skin is thinner and more permeable, stomach lacks acid to kill bacteria, lungs have weaker mucus barrier, liver and kidneys not fully developped, body temp not as well regulated ( more dehydration )
45