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  • !Receptor <br/> (↑ = opens. ↓ = closes) <ref name=boron/> <br> <font size=1> On [ |rowspan=2| [[nitric oxide]] || ↑[[NO receptor]] on smooth muscle || ↑[[cyclic GMP|cGMP]] --> ↑[[protein kinase g|PKG]
    13 KB (1,665 words) - 21:28, 21 September 2010
  • ...enin-Angiotensin System: Emphasis on Blockade of the Angiotensin II Type-1 Receptor ...(ARBs) can be used to prevent angiotensin II from acting on [[angiotensin receptor]]s.
    11 KB (1,520 words) - 12:30, 28 January 2012
  • ...tp://www.nature.com/bjp/journal/v143/n4/full/0705974a.html "Selective GABA-receptor actions of amobarbital on thalamic neurons."] ''British Journal of Pharmaco ...t (military)|frontline]].<ref>[http://www.pbs.org/wgbh/amex/bulge/filmmore/pt.html Use of sodium amytal during WWII]</ref>
    9 KB (1,128 words) - 22:04, 21 September 2010
  • ...month= November | year= 1975 | pages= 530&ndash;4 | volume= 18 | issue= (5 Pt 1) | pmid=1102231 | accessdate= 2008-02-22}}</ref><ref name="Phillips">{{ci ...ref> and there may be other modes of action such as through [[histamine H3 receptor]]s<ref name="Girard">{{cite journal | author= Girard P, Pansart Y, Coppé M
    9 KB (1,159 words) - 22:06, 21 September 2010
  • ...ervous]] and [[immune system]]s of animals and that activate [[cannabinoid receptor]]s , and 3. '''synthetic cannabinoids''', a structurally diverse class of m {{Main|Cannabinoid receptor}}
    49 KB (6,487 words) - 22:06, 21 September 2010
  • ...brain: isolation, structure elucidation, and interactions with the opiate receptor |journal=Proc Natl Acad Sci USA |volume=73 |issue=7 |pages=2515–9 |year=1 ...for the κ<sub>1</sub> opioid receptors. μ opioid receptors are the main receptor through which [[morphine]] acts. Classically, μ opioid receptors are presy
    18 KB (2,467 words) - 22:06, 21 September 2010
  • ...elieve minor throat irritation. Menthol also acts as a weak [[kappa Opioid receptor]] [[agonist]]. [[pt:Mentol]]
    15 KB (2,008 words) - 22:07, 21 September 2010
  • ...ub>1</sub>]] and [[CB2 receptor|CB<sub>2</sub>]] [[receptor_(biochemistry)|receptor]]s, with lower [[affinity_(pharmacology)|affinity]] in comparison to [[THC] [[pt:Canabinol]]
    3 KB (352 words) - 22:07, 21 September 2010
  • | url = http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0271-0749&volum ...affinity for [[Cannabinoid_receptor#CB1|CB<sub>1</sub>]] and [[Cannabinoid receptor#CB2|CB<sub>2</sub>]] receptors but acts as an indirect antagonist of cannab
    17 KB (2,198 words) - 22:07, 21 September 2010
  • ...|CB<sub>1</sub>]] receptor, which is the most abundant [[G protein-coupled receptor]] in the [[brain]]. ...inoid receptor]] antagonist [[rimonabant]] (SR141716A) as well as [[opioid receptor]] antagonists (opioid blockers) [[naloxone]] and [[naloxonazine]].<ref name
    50 KB (6,686 words) - 22:09, 21 September 2010
  • ...de Lamarck, J.B. 1785. ''Encyclopédie Méthodique de Botanique'', vol. 1, pt. 2. Paris, France, pp. 694-695</ref> Lamarck based his description of the n ...nabidiol modulates and directly activates alpha-1 and alpha-1-Beta glycine receptor function|journal = [[Pharmacology]]|volume = 83|issue = 4|pages = 217–222
    76 KB (10,798 words) - 22:10, 21 September 2010
  • ...f the amyloid precursor protein | journal = J. Cell. Sci. | volume = 113 ( Pt 11) | issue = | pages = 1857–70 | year = 2000 | month = June | pmid = 108 ...comparisons to the signaling role of the surface [[transmembrane receptor|receptor]] protein [[Notch signaling|Notch]].<ref name="Selkoe">{{cite journal | aut
    36 KB (4,595 words) - 22:11, 21 September 2010
  • || [[Dopamine receptor]]s at pathway terminations. ...gmental nuclei]] (''pontomesencephalotegmental complex'') || (mainly) [[M1 receptor]]s in:
    11 KB (1,374 words) - 22:11, 21 September 2010
  • ...=|accessdate=}}</ref>&nbsp; Signal transduction starts with a signal to a receptor, and ends with a change in cell function. ...de the cell.&nbsp; The chemical signal binds to the outer portion of the receptor, changing its shape and conveying another signal inside the cell.&nbsp; So
    55 KB (7,677 words) - 22:12, 21 September 2010
  • *Some [[transient receptor potential channel]]s: This group of channels, normally referred to simply a ...nion-permeable γ-aminobutyric acid-gated [[GABA receptor|GABA<sub>A</sub> receptor]].
    31 KB (4,177 words) - 22:12, 21 September 2010
  • Loperamide is an [[opioid]]-receptor [[agonist]] and acts on the [[Mu Opioid receptor|μ-opioid receptors]] in the [[myenteric plexus]] of the large intestine; b [[pt:Loperamida]]
    7 KB (989 words) - 22:12, 21 September 2010
  • ...antagonist|antagonist]] activity at the [[kappa opioid receptor|κ-opioid receptor]]. Buprenorphine [[hydrochloride]] was first marketed in the 1980s by Recki Suboxone contains buprenorphine as well as the [[opioid]] [[receptor antagonist|antagonist]] [[naloxone]] to deter the abuse of tablets by [[int
    59 KB (8,561 words) - 22:13, 21 September 2010
  • ...8}}</ref> In addition, it is a synthetic strong agonist at the [[mu opioid receptor|μ-opioid]] receptors. Historically it has been used to treat [[breakthroug [[pt:Fentanil]]
    33 KB (4,684 words) - 21:01, 24 September 2010
  • ...lly unlike [[morphine]] or [[heroin]], methadone also acts on the [[opioid receptor]]s and thus produces many of the same effects. Methadone is also used in ma ...receptor, but also has some affinity for the [[NMDA]] ionotropic glutamate receptor. It is metabolized by the enzymes [[CYP3A4]], [[CYP2B6]] and [[CYP2D6]], wi
    61 KB (8,865 words) - 22:13, 21 September 2010
  • ...2receptorsimplications for models of schizophrenia](2002)</ref> Other NMDA receptor antagonists include [[ketamine]], [[tiletamine]], and [[dextromethorphan]]. In a similar manner, PCP and analogues also inhibit [[nicotinic acetylcholine receptor]] channels (nAChR). Some analogues have greater potency at nAChR than at NM
    21 KB (3,002 words) - 21:02, 24 September 2010
  • ...potent [[Kappa Opioid receptor|κ-opioid]] and [[D2 receptor|D<sub>2</sub> receptor]] [[agonist]].<ref name="Zhang2005pabs" /><ref name="Seeman2009">[[#refSeem ...ain a [[Base (chemistry)|basic]] [[nitrogen]]), unlike most known [[opioid receptor]] [[ligand]]s.<ref name="Harding2006p107">[[#refHarding2006|Harding, Schmid
    133 KB (18,241 words) - 22:14, 21 September 2010
  • As a narcotic, hydrocodone relieves [[pain]] by binding to [[opioid receptor]]s in the [[brain]] and [[spinal cord]]. It can be taken with or without f [[pt:Diidrocodeína]]
    30 KB (4,151 words) - 22:14, 21 September 2010
  • ...ssociative]] [[hallucinogen]]. Its [[mechanism of action]] is as an [[NMDA receptor antagonist]], producing effects similar to those of the controlled substan ...7 | doi = 10.1097/ANA.0b013e31817f523f | url = http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0898-4921&volum
    26 KB (3,444 words) - 22:15, 21 September 2010
  • ...It has also been shown that Alfaxalone binds to a different region of this receptor than the benzodiazipines (2). Alfaxalone is metabolised rapidly in the live ...RL, et al. A single amino acid of the human gamma-aminobutyric acid type A receptor gamma 2 subunit determines benzodiazepine efficacy. J Biol Chem 1994;269:32
    3 KB (405 words) - 21:00, 24 September 2010
  • ...n]] [[protein dimer|dimer]] complex. The [[gene]] [[encoding]] an ethylene receptor has been cloned in ''[[Arabidopsis thaliana]]'' and then in [[tomato]]. Eth Ethylene hormone receptor action in Arabidopsis. Chang C, Stadler R. Bioessays. 2001 Jul;23(7):619-27
    32 KB (4,462 words) - 21:01, 24 September 2010
  • Etomidate is an agonist at [[GABAA receptor|GABA<sub>A</sub>]] [[Receptor (biochemistry)|receptors]]<ref>Vanlersberghe C, Camu F. Etomidate and other [[pt:Etomidato]]
    10 KB (1,350 words) - 21:01, 24 September 2010
  • ...Receptor antagonist|antagonist]] of N-methyl-d-aspartate receptors ([[NMDA receptor]]s). These receptors exacerbate the damage from [[oxygen deprivation]] and [[Category:NMDA receptor antagonists]]
    82 KB (11,842 words) - 21:02, 24 September 2010
  • ...l analogues: mapping binding sites for an anesthetic phenol on the GABA(A) receptor. ''Journal of Medicinal Chemistry''. 2002 Jul 18;45(15):3210–21. PMID 121 [[pt:Propofol]]
    21 KB (2,875 words) - 21:03, 24 September 2010
  • ...0s by Dr. [[Henri Laborit]] to use in studying the neurotransmitter [[GABA receptor|GABA]].<ref>{{cite journal | author = H. Laborit, J.M. Jouany, J. Gerald, F ...}</ref> and it is a weak agonist at the [[GABA receptor|GABA<sub>B</sub>]] receptor, which is [[inhibitory]].<ref name="mechanism" /> GHB is a naturally-occurr
    55 KB (7,839 words) - 21:04, 24 September 2010
  • [[ca:Receptor superheterodí]] [[es:Receptor superheterodino]]
    31 KB (4,651 words) - 14:50, 10 December 2011

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