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大麻素受体激动作用可抑制特发性震颤大鼠模型中的震颤、认知障碍和焦虑样行为。

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

作者信息

Abbassian Hassan, Esmaeili Parisa, Tahamtan Mahshid, Aghaei Iraj, Vaziri Zohreh, Sheibani Vahid, Whalley Benjamin J, Shabani Mohammad

机构信息

Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, 76198-13159, Iran.

Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Physiol Behav. 2016 Oct 1;164(Pt A):314-20. doi: 10.1016/j.physbeh.2016.06.013. Epub 2016 Jun 15.

Abstract

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 (0.5mg/kg; i.p.) 15min before harmaline administration (10mg/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.

摘要

认知和运动障碍是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,但一些潜在的治疗药物已被用于减轻震颤动物模型中的认知症状。在本研究中,研究了大麻素受体(CBR)激动剂WIN55,212-2(WIN)对harmaline诱导的运动和认知障碍的影响。成年大鼠在给予harmaline(10mg/kg;腹腔注射)前15分钟接受WIN(0.5mg/kg;腹腔注射)治疗,之后使用旷场行为和穿梭箱试验评估探索行为、焦虑相关行为和认知功能。与接受harmaline赋形剂处理的对照组相比,仅接受harmaline处理的大鼠进入中央方格的次数明显减少,而接受WIN和harmaline处理的大鼠与仅接受harmaline处理的大鼠相比,进入中央方格的次数显著增加。给予WIN可部分逆转harmaline处理大鼠中观察到的被动回避记忆障碍。本研究中证明的WIN的神经保护和抗焦虑作用表明,大麻素受体(CBR)激动剂作为一种潜在的神经保护剂,可用于治疗伴有精神功能障碍的震颤患者。

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