Search results

From Self-sufficiency
Jump to: navigation, search
  • ...ns predecessor agency. It is one of the most effective orally-administered opioid analgesics and has a wide safety margin. Its strength ranges from 8 to 12 p ...otably morphine, exert their effects by binding to and activating the μ-[[opioid receptor]].
    40 KB (5,581 words) - 16:45, 27 September 2010
  • ...sometimes added to potentially addictive drugs, particularly anti-diarrhea opioid drugs such as [[diphenoxylate]] or [[difenoxin]], wherein the secretion-red [[hu:Atropin]]
    16 KB (2,198 words) - 16:46, 27 September 2010
  • ...or=Hirota K, Sikand KS, Lambert DG |title=Interaction of ketamine with mu2 opioid receptors in SH-SY5Y human neuroblastoma cells |journal=Journal of Anesthes ...nting side effects.<ref name="elia" /> The combination of ketamine with an opioid is, however, particularly useful for pain caused by cancer.<ref>{{Cite jour
    69 KB (9,697 words) - 21:01, 24 September 2010
  • ...own effects on serotonin, fluoxetine also increases density of endogenous opioid receptors<ref>{{cite journal |author=de Gandarias JM, Echevarría E, Acebes [[hu:Fluoxetin]]
    52 KB (7,168 words) - 16:47, 27 September 2010
  • ==== Opioid and cannabinoid transmission ==== [[Opioid]] and [[cannabinoid]] transmission instead of dopamine may modulate consumm
    48 KB (6,470 words) - 16:48, 27 September 2010
  • ...ite journal| author=Volans G, Hartley V, McCrea S, Monaghan J. | title=Non-opioid analgesic poisoning | journal=Clinical Medicine | year=2003 | pages=119–2 [[hu:Ibuprofén]]
    29 KB (3,955 words) - 22:17, 21 September 2010
  • ...of N<sub>2</sub>O.<ref name="branda"/> Several experiments have shown that opioid receptor antagonists applied directly to the brain block the antinociceptiv ...1463.x}}</ref> Exactly how N<sub>2</sub>O causes the release of endogenous opioid peptides is still uncertain.
    61 KB (8,728 words) - 16:50, 27 September 2010
  • *Other [[opiate]]s and [[opioid]]s ([[narcotic]]s or [[analgesic]]s) ...]] [[analgesic]] [[medication]] and is considered to be the prototypical [[opioid]]. It was discovered in 1804 by Sertürner, first distributed by same in 1
    87 KB (12,376 words) - 16:51, 27 September 2010
  • ...[[common cold|cold]] and [[Influenza|flu]] remedies. In combination with [[opioid analgesic]]s, paracetamol can also be used in the management of more severe In some formulations, paracetamol is combined with the [[opioid]] [[codeine]], sometimes referred to as [[co-codamol]] ([[British Approved
    54 KB (7,376 words) - 16:52, 27 September 2010
  • ...etoacidosis]], [[meningitis]], [[methemoglobinemia]], or [[Opioid overdose|opioid]] or toxic alcohol poisoning.<ref name="emedicine"/> [[hu:Szénmonoxid-mérgezés]]
    71 KB (9,723 words) - 21:31, 20 September 2010
  • '''Endorphins''' ("'''endo'''genous mo'''rphin'''e") are [[endogenous]] [[opioid]] [[peptide]]s that function as [[neurotransmitters]].<ref>Oswald Steward: [[Opioid peptide|Opioid neuropeptides]] were first discovered in 1974 by two independent groups of
    18 KB (2,467 words) - 22:06, 21 September 2010
  • ...ed to relieve minor throat irritation. Menthol also acts as a weak [[kappa Opioid receptor]] [[agonist]]. ...esic]] properties that are mediated through a selective activation of κ-[[opioid receptors]].<ref>{{cite journal | author = Galeottia, N., Mannellia, L.D.C.
    15 KB (2,008 words) - 22:07, 21 September 2010
  • ...ist [[rimonabant]] (SR141716A) as well as [[opioid receptor]] antagonists (opioid blockers) [[naloxone]] and [[naloxonazine]].<ref name="Lupica 2004">{{cite ...d YL|date=2007|title=Adolescent cannabis exposure alters opiate intake and opioid limbic neuronal populations in adult rats|journal=Neuropsychopharmacology|v
    50 KB (6,686 words) - 22:09, 21 September 2010
  • ...spx?CdrID=41911 US National Cancer Institute, Drug Dictionary]</ref> is an opioid [[medication|drug]] effective against [[diarrhea]] resulting from [[gastroe ...an [[opioid]]-receptor [[agonist]] and acts on the [[Mu Opioid receptor|μ-opioid receptors]] in the [[myenteric plexus]] of the large intestine; by itself i
    7 KB (989 words) - 22:12, 21 September 2010
  • ...diction in higher dosages (>2&nbsp;mg) and to control moderate pain in non-opioid tolerant individuals in lower dosages (~200&nbsp;µg). ...uprenorphine's high-dose sublingual pill preparations, were approved for [[opioid]] addiction treatment in September 2006. In the [[Netherlands]], Buprenorph
    59 KB (8,561 words) - 22:13, 21 September 2010
  • ...ereof and, therefore, a semi-synthetic drug. It is, in medical terms, an [[opioid]] analgesic and, in legal terms, a [[narcotic]]. It should not be confused ...eating]].<ref name="rxlist.com"/> Massive overdoses are rarely observed in opioid-tolerant individuals, but, when they occur, they may lead to circulatory sy
    38 KB (5,300 words) - 22:13, 21 September 2010
  • ...addition, it is a synthetic strong agonist at the [[mu opioid receptor|μ-opioid]] receptors. Historically it has been used to treat [[breakthrough pain|chr ...tanyl by assaying analogues of the structurally-related drug pethidine for opioid activity.<ref>{{cite journal|doi=10.1021/jm040195b|url=http://www.pauljanss
    33 KB (4,684 words) - 21:01, 24 September 2010
  • ...chemically unlike [[morphine]] or [[heroin]], methadone also acts on the [[opioid receptor]]s and thus produces many of the same effects. Methadone is also u ...on of effect. Oral doses of methadone can stabilise patients by mitigating opioid [[withdrawal]] syndrome. Higher doses of methadone can block the euphoric e
    61 KB (8,865 words) - 22:13, 21 September 2010
  • ...nits - this may well be mediated by the lack of related efficacy at the mu-opioid receptor, though the NMDAR certainly does play a role in transmission of pa [[hu:Fenciklidin]]
    21 KB (3,002 words) - 21:02, 24 September 2010
  • ...potential]];<ref name="Zhang2005pabs" /><ref name="Valdés1983" /> as a κ-opioid agonist. ...ot contain a [[Base (chemistry)|basic]] [[nitrogen]]), unlike most known [[opioid receptor]] [[ligand]]s.<ref name="Harding2006p107">[[#refHarding2006|Hardin
    133 KB (18,241 words) - 22:14, 21 September 2010

View (previous 20 | next 20) (20 | 50 | 100 | 250 | 500)