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..., Aoki K, Takagi M, Miyatake M, Suzuki T |title=A putative sigma1 receptor antagonist NE-100 attenuates the discriminative stimulus effects of ketamine in rats | ...ranados et al |title= A Randomized Add-on Trial of an N-methyl-D-aspartate Antagonist in Treatment-Resistant Bipolar Depression|journal=Archives of General Psych

...>3</sub> receptor]] antagonist/[[5-HT receptor|5-HT₄ receptor]] agonist. ...ingstone; 2003. ISBN 0-443-07145-4</ref> At higher doses, 5-HT₃ antagonist activity may also contribute to the anti-emetic effect.

...and Type II receptor agonist), or [[RU28362]] (a specific Type II receptor agonist), to adrenalectomized animals induced changes in [[leukocyte distribution]] ...aims in their marketing that CortiSlim is a cortisol [[Receptor antagonist|antagonist]].<ref name=Iwata>{{Cite news|author=Iwata, Edward |title=Diet pill sellers

...ategories. Antihistamines like cyclizine and tripelennamine are sometimes mixed with morphine to increase both, a potentially dangerous practise via unsupe ...ate some counter-regulatory pathways responsible for opioid tolerance. CCK-antagonist drugs, specifically [[proglumide]], have been shown to slow the development

...at= |work=}}</ref> It has been hypothesized that CBD acts as an allosteric antagonist at the CB₁ receptor and thus alters the psychoactive effects of ...ly potent alpha(2)-adrenoceptor agonist and moderately potent 5HT receptor antagonist | journal = British Journal of Pharmacology | volume = 159| issue = 1| page

...alongside a more potent CB₁ agonist, but exhibits weak partial agonist effects when administered by itself.<ref>{{Cite pmid|10323589}}</ref><ref>{

...Fernando SR, Griffin G, Ryan W, Razdan RK, Compton DR, Martin BR. Agonist-antagonist characterization of 6'-cyanohex-2'-yne-delta 8-tetrahydrocannabinol in two

...id receptor|δ-opioid receptor]], and competitive [[competitive antagonist|antagonist]] activity at the [[kappa opioid receptor|κ-opioid receptor]]. Buprenorphi ...However, the Suboxone formulation still has potential to produce an opioid agonist "high" if injected by non-dependent persons which may provide some explanat

...of [[dissociative anesthetic]]s. PCP works primarily as an [[NMDA receptor antagonist]], which blocks the activity of the [[NMDA receptor]] and, like most antigl ...y (pharmacology)|potent]] [[D2 receptor|D₂ receptor]] [[partial agonist]]s,<ref name="pmid19391150">{{cite journal | unused_data = DUPLICATE DATA:

.../ms_papier/e-docs/00/00/06/F7/document_article.md}}</ref> and it is a weak agonist at the [[GABA receptor|GABA_B]] receptor, which is [[inhibitory]] ...5 to 3 hours, or even longer if large doses have been consumed or if it is mixed with alcohol.<ref name=GALL1>{{cite journal |author=Galloway GP, Frederick-