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  2. Drug action - Wikipedia

    en.wikipedia.org/wiki/Drug_action

    The action of drugs on the human body (or any other organism's body) is called pharmacodynamics, and the body's response to drugs is called pharmacokinetics. The drugs that enter an individual tend to stimulate certain receptors, ion channels, act on enzymes or transport proteins. As a result, they cause the human body to react in a specific way.

  3. Mechanism of action - Wikipedia

    en.wikipedia.org/wiki/Mechanism_of_action

    Common examples of drugs that work in this way are antacids and laxatives. [ 2 ] In contrast, a mode of action (MoA) describes functional or anatomical changes, at the cellular level, resulting from the exposure of a living organism to a substance.

  4. Pharmacodynamics - Wikipedia

    en.wikipedia.org/wiki/Pharmacodynamics

    Topics of pharmacodynamics. Pharmacodynamics (PD) is the study of the biochemical and physiologic effects of drugs (especially pharmaceutical drugs).The effects can include those manifested within animals (including humans), microorganisms, or combinations of organisms (for example, infection).

  5. Pharmacology - Wikipedia

    en.wikipedia.org/wiki/Pharmacology

    Pharmacology can also focus on specific systems comprising the body. Divisions related to bodily systems study the effects of drugs in different systems of the body. These include neuropharmacology, in the central and peripheral nervous systems; immunopharmacology in the immune system.

  6. Category:Drugs that are a physiological drug - Wikipedia

    en.wikipedia.org/wiki/Category:Drugs_that_are_a...

    {{Infobox drug}} articles that have Physiological parameters input: <!-- Physiology --> | source_tissues = | target_tissues = | receptors = | agonists = | antagonists = | precursor = | biosynthesis = Note: |metabolism= will only show in the Physiologic data section when other input is present. Same for metabolism input under the pharmacokinetic ...

  7. Distribution (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Distribution_(pharmacology)

    Therefore, the chemical characteristics of a drug will determine its distribution within an organism. For example, a liposoluble drug will tend to accumulate in body fat and water-soluble drugs will tend to accumulate in extracellular fluids. The volume of distribution (V D) of a drug is a property that quantifies the extent of its distribution ...

  8. Here's how long various drugs stay in your body - AOL

    www.aol.com/article/2016/02/21/heres-how-long...

    In the process, metabolites, or byproducts, of the drug are produced, which can linger in our blood, urine (and even in our hair) for long after the initial effects of the drug are felt.

  9. Physiological agonism and antagonism - Wikipedia

    en.wikipedia.org/wiki/Physiological_agonism_and...

    Physiological agonism describes the action of a substance which ultimately produces the same effects in the body as another substance—as if they were both agonists at the same receptor—without actually binding to the same receptor.