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  2. Atipamezole - Wikipedia

    en.wikipedia.org/wiki/Atipamezole

    Atipamezole is a competitive antagonist at ɑ 2-adrenergic receptors that competes with dexmedetomidine, an ɑ 2-adrenergic receptors agonist. It does not directly interact with dexmedetomidine; [34] rather, their structural similarity allows atipamezole to easily compete for receptor binding sites. [12]

  3. Dexmedetomidine - Wikipedia

    en.wikipedia.org/wiki/Dexmedetomidine

    Dexmedetomidine, sold under the trade name Precedex among others, is a drug used in humans for sedation. [4] Veterinarians use dexmedetomidine for similar purposes in treating cats, dogs, and horses. [ 8 ] [ 9 ] It is also used in humans to treat acute agitation associated with schizophrenia or bipolar disorder . [ 5 ]

  4. Medetomidine - Wikipedia

    en.wikipedia.org/wiki/Medetomidine

    Medetomidine is a racemic mixture of two optical or stereoisomers, levomedetomidine and dexmedetomidine. [4] The latter causes the alpha 2- adrenergic agonist effects. [5] It is often used as the hydrochloride salt, medetomidine hydrochloride, a crystalline white solid that can be administered as an intravenous drug solution with sterile water.

  5. Alpha-2 blocker - Wikipedia

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

    They are mainly used in research, having found limited clinical application in human medicine. They are extensively used in veterinary medicine to reverse the effects of alpha-2 agonist drugs used as sedatives, like xylazine, medetomidine and dexmedetomidine. Alpha-2 blockers increase noradrenaline release.

  6. I've cracked the code on feline love – here are the sweetest ...

    www.aol.com/lifestyle/ive-cracked-code-feline...

    Some cats are just complete velcro kitties — yes, we’re looking at you, Miss Siamese! These high-maintenance cat breeds can’t imagine being separated from their humans or missing out on any ...

  7. Detomidine - Wikipedia

    en.wikipedia.org/wiki/Detomidine

    Detomidine is a sedative with analgesic properties. [3] α2-adrenergic agonists produce dose-dependent sedative and analgesic effects, mediated by activation of α2 catecholamine receptors, thus inducing a negative feedback response, reducing production of excitatory neurotransmitters.

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