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ACP-103是一种5-羟色胺2A受体反向激动剂,在实验模型中可提高氟哌啶醇和利培酮的抗精神病疗效及改善副作用情况。

ACP-103, a 5-hydroxytryptamine 2A receptor inverse agonist, improves the antipsychotic efficacy and side-effect profile of haloperidol and risperidone in experimental models.

作者信息

Gardell Luis R, Vanover Kimberly E, Pounds Linda, Johnson Robert W, Barido Richard, Anderson Gary T, Veinbergs Isaac, Dyssegaard Agnete, Brunmark Per, Tabatabaei Ali, Davis Robert E, Brann Mark R, Hacksell Uli, Bonhaus Douglas W

机构信息

ACADIA Pharmaceuticals, Inc., 3911 Sorrento Valley Blvd., San Diego, CA 92121, USA.

出版信息

J Pharmacol Exp Ther. 2007 Aug;322(2):862-70. doi: 10.1124/jpet.107.121715. Epub 2007 May 22.

Abstract

Dopamine D(2) receptor antagonism contributes to the therapeutic action of antipsychotic drugs (APDs) but also produces undesirable side effects, including extrapyramidal motor deficits, cognitive dulling, and prolactinemia. The introduction of atypical APDs was a significant advancement in the treatment of schizophrenia. Whereas these agents are D(2) receptor antagonists, they are also potent 5-hydroxytryptamine (5-HT)(2A) receptor inverse agonists, a feature that may explain their improved efficacy and tolerability. Recently, we reported that N-(4-fluorophenylmethyl)-N-(1-methylpiperidin-4-yl)-N'-(4-(2-methylpropyloxy)phenylmethyl) carbamide (2R,3R)-dihydroxybutanedioate (2:1) (ACP-103), a novel selective 5-HT(2A) receptor inverse agonist that fails to bind D(2) receptors, is active in several models predictive of antipsychotic activity. Using ACP-103, we tested the hypothesis that combining high levels of 5-HT(2A) inverse agonism with low levels of D(2) antagonism would result in a favorable interaction, such that antipsychotic efficacy could be achieved with reduced D(2) receptor-related adverse effects. Here we show that ACP-103 1) potently inhibited head-twitching produced by the 5-HT(2A/2C) receptor agonist (+/-)-2,5-dimethoxy-4-iodoamphetamine, 2) increased the potency of haloperidol against amphetamine-induced hyperactivity, 3) interacted synergistically with haloperidol or risperidone to suppress hyperactivity induced by the N-methyl-d-aspartate receptor antagonist (5R,10S)-(+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine hydrogen maleate (MK-801), and, by contrast, 4) attenuated haloperido-l- or risperidone-induced prolactinemia. ACP-103 also attenuated catalepsy produced by haloperidol or risperidone. However, the doses that were required for this effect were higher than would be expected for a 5-HT(2A) receptor-mediated mechanism. These data indicate that utilizing ACP-103 as an adjunctive therapy to currently used APDs may result in enhanced antipsychotic efficacy while reducing adverse effects including those attributable to D(2) receptor antagonism.

摘要

多巴胺D(2)受体拮抗作用有助于抗精神病药物(APD)的治疗作用,但也会产生不良副作用,包括锥体外系运动缺陷、认知迟钝和高催乳素血症。非典型APD的引入是精神分裂症治疗的一项重大进展。虽然这些药物是D(2)受体拮抗剂,但它们也是强效的5-羟色胺(5-HT)(2A)受体反向激动剂,这一特性可能解释了它们更好的疗效和耐受性。最近,我们报道了N-(4-氟苄基)-N-(1-甲基哌啶-4-基)-N'-(4-(2-甲基丙氧基)苄基)脲(2R,3R)-二羟基丁二酸酯(2:1)(ACP-103),一种新型的选择性5-HT(2A)受体反向激动剂,它不与D(2)受体结合,在几种预测抗精神病活性的模型中具有活性。使用ACP-103,我们检验了这样一个假设,即高水平的5-HT(2A)反向激动作用与低水平的D(2)拮抗作用相结合会产生有利的相互作用,从而在减少D(2)受体相关不良反应的情况下实现抗精神病疗效。在此我们表明,ACP-103 1)有效抑制5-HT(2A/2C)受体激动剂(±)-2,5-二甲氧基-4-碘苯丙胺引起的头部抽搐,2)增强氟哌啶醇对苯丙胺诱导的多动的效力,3)与氟哌啶醇或利培酮协同作用以抑制N-甲基-D-天冬氨酸受体拮抗剂(5R,10S)-(+)-5-甲基-10,11-二氢-5H-二苯并[a,d]环庚烯-5,10-亚胺马来酸氢盐(MK-801)诱导的多动,相反,4)减弱氟哌啶醇或利培酮诱导的高催乳素血症。ACP-103还减弱了氟哌啶醇或利培酮引起的僵住症。然而,产生这种作用所需的剂量高于5-HT(2A)受体介导机制所预期的剂量。这些数据表明,将ACP-103用作目前使用的APD的辅助治疗可能会提高抗精神病疗效,同时减少包括那些归因于D(2)受体拮抗作用的不良反应。

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