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  2. Alpha-adrenergic agonist - Wikipedia

    en.wikipedia.org/wiki/Alpha-adrenergic_agonist

    The alpha-adrenergic receptor has two subclasses α 1 and α 2. Alpha 2 receptors are associated with sympatholytic properties. Alpha-adrenergic agonists have the opposite function of alpha blockers. Alpha adrenoreceptor ligands mimic the action of epinephrine and norepinephrine signaling in the heart, smooth muscle and central nervous system, with

  3. Clonidine - Wikipedia

    en.wikipedia.org/wiki/Clonidine

    Clonidine, sold under the brand name Catapres among others, is an α 2A-adrenergic receptor agonist [12] medication used to treat high blood pressure, ADHD, drug withdrawal (e.g., alcohol, opioids, or nicotine), menopausal flushing, diarrhea, spasticity, and certain pain conditions. [13] The drug is often prescribed off-label for tics.

  4. Tizanidine - Wikipedia

    en.wikipedia.org/wiki/Tizanidine

    It is an α 2-adrenergic agonist, but how it works is not entirely clear. [5] Tizanidine was approved for medical use in the United States in 1996. [5] It is available as a generic medication. [3] In 2022, it was the 94th most commonly prescribed medication in the United States, with more than 6 million prescriptions. [7] [8]

  5. Alpha-2 adrenergic receptor - Wikipedia

    en.wikipedia.org/wiki/Alpha-2_adrenergic_receptor

    In non-human species this is an immobilizing and anesthetic drug, presumptively also mediated by α 2 adrenergic receptors because it is reversed by yohimbine, an α 2 antagonist. α 2A selective agonists include guanfacine (an antihypertensive) and brimonidine (UK 14,304). -3-nitrobiphenyline is an α 2C selective agonist as well as being a ...

  6. Gabapentinoid - Wikipedia

    en.wikipedia.org/wiki/Gabapentinoid

    The gabapentinoid drugs do not bind significantly to other known drug receptors and so the α 2 δ VGCC subunit has been called the gabapentin receptor. [ 15 ] [ 4 ] Recently, the same α 2 δ-1 protein has been found closely associated not with VGCCs but with other proteins such as presynaptic NMDA-type glutamate receptors , cell adhesion ...

  7. FDA approves new pain medication as an alternative to opioids ...

    www.aol.com/fda-approves-pain-medication...

    The FDA on Thursday approved a new class of pain medication that provides an alternative to opioids. It will be sold under the brand name Journavx. ... FDA approval of Journavx comes after 2 drug ...

  8. FDA approves new type of non-opioid pain medication, 1st of ...

    www.aol.com/fda-approves-type-non-opioid...

    This is the first class of non-opioid pain medication approved to treat moderate to severe acute pain approved by the FDA in more than 20 years. FDA approves new type of non-opioid pain medication ...

  9. Adrenergic receptor - Wikipedia

    en.wikipedia.org/wiki/Adrenergic_receptor

    The adrenergic receptors or adrenoceptors are a class of G protein-coupled receptors that are targets of many catecholamines like norepinephrine (noradrenaline) and epinephrine (adrenaline) produced by the body, but also many medications like beta blockers, beta-22) antagonists and alpha-22) agonists, which are used to treat high ...