首页> 美国卫生研究院文献>Frontiers in Psychiatry >Translational Aspects of the Novel Object Recognition Task in Rats Abstinent Following Sub-Chronic Treatment with Phencyclidine (PCP): Effects of Modafinil and Relevance to Cognitive Deficits in Schizophrenia
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Translational Aspects of the Novel Object Recognition Task in Rats Abstinent Following Sub-Chronic Treatment with Phencyclidine (PCP): Effects of Modafinil and Relevance to Cognitive Deficits in Schizophrenia

机译:苯环利定(PCP)亚慢性治疗后戒断的大鼠中新型对象识别任务的翻译方面:莫达非尼的影响和与精神分裂症认知缺陷的相关性。

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摘要

Phencyclidine (PCP) induces a behavioral syndrome in rodents that bears remarkable similarities to some of the core symptoms observed in schizophrenic patients, among those cognitive deficits. The successful alleviation of cognitive impairments associated with schizophrenia (CIAS) has become a major focus of research efforts as they remain largely untreated. The aim of the present study was to investigate the effects of selected antipsychotic and cognition enhancing drugs, namely haloperidol, risperidone, donepezil, and modafinil in an animal model widely used in preclinical schizophrenia research. To this end, the novel object recognition (NOR) task was applied to rats abstinent following sub-chronic treatment with PCP. Rats were administered either PCP (5 mg/kg, i.p.) or vehicle twice a day for 7 days, followed by a 7-day washout period, before testing in NOR. Upon testing, vehicle-treated rats successfully discriminated between novel and familiar objects, an effect abolished in rats that had previously been exposed to PCP treatment. Acute treatment with modafinil (64 mg/kg, p.o.) ameliorated the PCP-induced deficit in novel object exploration, whereas haloperidol (0.1 mg/kg, s.c.), risperidone (0.2 mg/kg, i.p.), and donepezil (3 mg/kg, p.o.) were without significant effect. Given the negligible efficacy of haloperidol and risperidone, and the contradictory data with donepezil to treat CIAS in the clinic, together with the promising preliminary pro-cognitive effects of modafinil in certain subsets of schizophrenic patients, the sub-chronic PCP–NOR abstinence paradigm may represent an attractive option for the identification of potential novel treatments for CIAS.
机译:苯环利定(PCP)在啮齿动物中诱发一种行为综合症,与那些认知缺陷中在精神分裂症患者中观察到的一些核心症状具有显着相似性。成功地减轻与精神分裂症(CIAS)相关的认知障碍已成为研究工作的主要重点,因为它们仍未得到治疗。本研究的目的是在广泛用于临床精神分裂症研究的动物模型中研究选定的抗精神病药物和增强认知的药物氟哌啶醇,利培酮,多奈哌齐和莫达非尼的作用。为此,将新型对象识别(NOR)任务应用于PCP亚慢性治疗后戒断的大鼠。每天两次给大鼠施用PCP(5μg/ kg,腹腔注射)或赋形剂,持续7 d天,随后是7天的清除期,然后再进行NOR测试。经测试,用载剂处理的大鼠成功地区分了新颖的物体和熟悉的物体,这种作用在先前接受过PCP治疗的大鼠中消失了。莫达非尼(64μmg/ kg,口服)的急性治疗改善了PCP诱导的新对象探索中的缺陷,而氟哌啶醇(0.1μmg/ kg,sc),利培酮(0.2μmg/ kg,ip)和多奈哌齐(3μmg/公斤,po)无明显影响。鉴于氟哌啶醇和利培酮的疗效可忽略不计,并且多奈哌齐在临床上用于治疗CIAS的数据相互矛盾,再加上莫达非尼在某些精神分裂症患者亚组中具有前瞻性的初步认知作用,因此亚慢性PCP-NOR戒断范例可能对于鉴定CIAS的潜在新疗法,是一个有吸引力的选择。

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