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45 Cards in this Set
- Front
- Back
why learn pharmacodynamics?
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educate patients, make prn decisions, evaluate pt. for drug responses, both beneficial and harmful, conferring w/ physicians
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What is defined as the study of the biochemical and physiologic effects of drugs and the molecular mechanisms by which those effects are produced.
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Pharmodynamics
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what determines the minimum amount of drug we can use, the maximum response a drug can elicit, and how much we need to increase the dosage to produce the desired increase in response
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dose response relationship
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another term for the relationship between the size of an administered dose and the intensity of the response produced.
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dose response relationship
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what are the two characteristic properties of drugs
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maxiaml efficacy and relative potency
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what is defined as the largest effect that a drug can produce
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maximal efficacy
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what is indicated by the height of the dose response curve
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maximal efficacy
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what term refers to the amount of drug we must give to elicit an effect
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potency
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what is indicated by the relative position of the dose response curve along the x (dose) axis
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potency
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True or False
potency of a drug implies nothing about its maximal efficacy. |
true
potency and efficacy are completely independent qualities |
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what are the special chemicals in the body that most drugs interact with to produce effects
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receptors
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what is the formal definition of any functional macromolecule in a cell to which a drug binds to produce its effects
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receptor
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what is generally reserved for what is arguably the most important group of macromolecules through which drugs act: the body's own receptors for hormones, neurotransmitter, adn other regulatory molecules.
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the term receptor
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what are normal points of physiologic processes
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receptors
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it is regulated by molecules supplied by the body
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receptor function
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what can drugs do at receptors
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they mimic or block the action of the body's own regulatory molecules
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drugs can or cannot give cells new functions
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cannot drugs cannot make the body do anything that it is not already capable fo doing
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what helps the body help itself
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medications
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what makes selective drug action possible
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by the existence of many types fo receptors, each regulating just a few processes.
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even though a drug is selective for only one type of receptor, is it possible fro that drug to produce nonselective effects?
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yes, if a single receptor type is responsibele for regulating several physiologic processes, then drugs that interact with that receptor will also influence a variety of processes.
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does selectivity guarantee safety
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no a compound can be highly selecive for one particular receptor and still be dangerous
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Two theories of drug receptro interaction
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simple occupancy theory and the modified occupancy theory
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what do the theories of drug receptor interaction help explain
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explain dose-response relationships and the ability of drugs to mimic or block the actions of endogenous regulatory molecules
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what states the intensity of the response to a drug is proportional to the number of receptors occupied by that drug and that a maximal response will occur when all available receptors have been occupied
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simple occupancy theory
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according to this theory two drugs acting at the same receptor should produce the same maximal effect, providing that their dosages were high enough to produce 100% receptor occupancy
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simple occupancy theory
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what ascribes two qualities to drugs: affinity and intrinsic activity
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the modified theory
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what refers to the strenght of the attraction between a drug and its receptor.
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affinity
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the affinity of a drug for its receptors is reflected in its
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potency
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drugs with high affinity are
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very potent
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this term refers to the ability of a drug to activate a receptor upon binding.
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intrinsic activity
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the intrinsic activity of a drug is reflected in its
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maximal efficacy.
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drugs with high intrinsic activity have high
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maximal efficacy.
that is by causing intense receptor activation, they are able to cause intense respnses, conversly if intrinsic activity is low, maximal efficacy will be low as well |
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are molecules taht activate receptors
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agonists
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because neurotransmitters, hormones, and all other endogenous regulators of receptor function activate the receptors to which they bind all of these compounds are considered
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agonists
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affinity allows the agonist to bind to receptors, while intrinsic activity allows the bound agonist to
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activate or turn on receptor function
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many therapeutic agents produce their effects by functioning as
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agonists
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what is an agonist that has only moderate intrinsic activity
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partial agonists
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what can act as an agonist as well as an antagonists
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partial agonists
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antagonists produce their effects by
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preventing the activation of receptors by agonists
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in terms fo the modified occupancy theory, an agonist is a drug that has both
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affinity and high intrinsic activity.
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when drugs bind to receptors they can do one of two things
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they can either mimic the action of endogenous regulatory molecules or they can block the action of endogenous regulatory molecules
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drugs that mimic the body's own regulatory molecues are called
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agonists
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drugs that block the actions of endogenous regulators are called
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antagonists
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mimic the actions of endogenous regulatory molecules, but they produce responses of intermediate intensity
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partial agonists
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how would you describe the action of rosiglitazone??
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it binds to a receptor to elicit a desired response, it binds to a receptor to prevent action fo another substance, it dislodges another substance from a receptor site
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