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首页> 外文期刊>Psychopharmacology >Group II mGluR agonist LY354740 and NAAG peptidase inhibitor effects on prepulse inhibition in PCP and d-amphetamine models of schizophrenia
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Group II mGluR agonist LY354740 and NAAG peptidase inhibitor effects on prepulse inhibition in PCP and d-amphetamine models of schizophrenia

机译:II组mGluR激动剂LY354740和N​​AAG肽酶抑制剂对精神分裂症PCP和d-苯异丙胺模型中的前脉冲抑制作用

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摘要

Group II metabotropic glutamate receptor (mGluR) agonists represent a novel approach to the treatment of schizophrenia. Inasmuch as the peptide neurotransmitter N-acetylaspartylglutamate (NAAG) activates these receptors, NAAG peptidase inhibitors conceptually represent a parallel path toward development of new antipsychotic drugs. While group II agonists are effective in several animal models of schizophrenia, they are reported to lack efficacy in moderating the effects of phencyclidine (PCP) on prepulse inhibition of acoustic startle in animal models of sensory processing deficits found in this disorder.
机译:II组代谢型谷氨酸受体(mGluR)激动剂代表了治疗精神分裂症的新方法。由于肽神经递质N-乙酰天冬氨酰谷氨酸(NAAG)激活了这些受体,因此NAAG肽酶抑制剂在概念上代表了开发新型抗精神病药物的平行途径。虽然II组激动剂在多种精神分裂症动物模型中有效,但据报道,在这种疾病的感觉加工缺陷动物模型中,它们缺乏调节苯环利定(PCP)对听觉惊吓的抑制作用的功效。

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