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Cannabinoid receptor agonism suppresses tremor, cognition disturbances and anxiety-like behaviors in a rat model of essential tremor

机译:大麻受体激动剂可抑制大鼠原发性震颤模型的震颤,认知障碍和焦虑样行为

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摘要

Cognitive and motor disturbances are serious consequences of tremor induced by motor disorders. Despite a lack of effective clinical treatment, some potential therapeutic agents have been used to alleviate the cognitive symptoms in the animal models of tremor. In the current study, the effects of WIN55, 212-2 (WIN), a cannabinoid receptor (CBR) agonist, on harmaline-induced motor and cognitive impairments were studied. Adult rats were treated with WIN (0.5 mg/kg; i.p.) 15 min before harmaline administration (10 mg/kg; ip) after which exploratory and anxiety related behaviors, and cognitive function were assessed using open-field behavior and shuttle box tests. Rats that received harmaline only exhibited a markedly reduced number of central square entries when compared to harmaline vehicle-treated controls, whereas those treated with WIN and harmaline showed a significant increase in central square entries, compared to harmaline only treated. The passive avoidance memory impairments observed in harmaline treated rats, was reversed somewhat by administration of WIN. The neuroprotective and anxiolytic effects of WIN demonstrated in the current study can be offered cannabinoid receptor (CBR) agonism as a potential neuroprotective agent in the treatment of patients with tremor that manifest mental dysfunctions. (C) 2016 Elsevier Inc All rights reserved.
机译:认知障碍和运动障碍是由运动障碍引起的震颤的严重后果。尽管缺乏有效的临床治疗方法,一些潜在的治疗剂已被用于减轻震颤动物模型中的认知症状。在当前的研究中,研究了大麻素受体(CBR)激动剂WIN55、212-2(WIN)对harmaline引起的运动和认知障碍的影响。成年大鼠在服用harmaline(10 mg / kg; ip)前15分钟接受WIN(0.5 mg / kg;腹膜内)治疗,之后使用开放视野行为和穿梭箱试验评估探索性和焦虑性行为以及认知功能。与接受harmaline媒介物治疗的对照组相比,接受harmaline的大鼠仅表现出明显减少的中央正方形入口,而与仅接受harmaline的大鼠相比,用WIN和harmaline治疗的大鼠的中央正方形进入显着增加。通过服用WIN可以逆转在接受harmaline治疗的大鼠中观察到的被动回避记忆障碍。当前研究证明的WIN的神经保护和抗焦虑作用可为大麻素受体(CBR)激动提供潜在的神经保护剂,用于治疗表现为精神功能障碍的震颤患者。 (C)2016 Elsevier Inc保留所有权利。

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