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  2. Reverse tolerance - Wikipedia

    en.wikipedia.org/wiki/Reverse_tolerance

    Reverse tolerance or drug sensitization is a pharmacological phenomenon describing subjects' increased reaction (positive or negative) to a drug following its repeated use. [4] Not all drugs are subject to reverse tolerance. This is the opposite of drug tolerance, in which the effect or the subject's reaction decreases following its repeated ...

  3. Drug tolerance - Wikipedia

    en.wikipedia.org/wiki/Drug_tolerance

    This may be caused by an increase in induction of the enzymes required for degradation of the drug e.g. CYP450 enzymes. This is most commonly seen with substances such as ethanol. This type of tolerance is most evident with oral ingestion, because other routes of drug administration bypass first-pass metabolism. Enzyme induction is partly ...

  4. Agonist-antagonist - Wikipedia

    en.wikipedia.org/wiki/Agonist-antagonist

    Agonist vs. antagonist. In pharmacology the term agonist-antagonist or mixed agonist/antagonist is used to refer to a drug which under some conditions behaves as an agonist (a substance that fully activates the receptor that it binds to) while under other conditions, behaves as an antagonist (a substance that binds to a receptor but does not activate and can block the activity of other agonists).

  5. Drug antagonism - Wikipedia

    en.wikipedia.org/wiki/Drug_antagonism

    Drug antagonism refers to a medicine stopping the action or effect of another substance, preventing a biological response. [ 1 ] [ 2 ] The stopping actions are carried out by four major mechanisms, namely chemical, pharmacokinetic , receptor and physiological antagonism . [ 2 ]

  6. Bioavailability - Wikipedia

    en.wikipedia.org/wiki/Bioavailability

    Therefore, a drug given by the intravenous route will have an absolute bioavailability of 100% (f = 1), whereas drugs given by other routes usually have an absolute bioavailability of less than one. If we compare the two different dosage forms having same active ingredients and compare the two drug bioavailability is called comparative ...

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  8. Antagonism (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Antagonism_(chemistry)

    The word is most commonly used in this context in biochemistry and toxicology: interference in the physiological action of a chemical substance by another having a similar structure. For instance, a receptor antagonist is an agent that reduces the response that a ligand produces when the receptor antagonist binds to a receptor on a cell .

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