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首页> 外文期刊>Brain research bulletin >Effects of baclofen on reserpine-induced vacuous chewing movements in mice.
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Effects of baclofen on reserpine-induced vacuous chewing movements in mice.

机译:巴氯芬对利血平诱导的小鼠空泡咀嚼运动的影响。

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We have described that GABA mimetic drugs present the ability to inhibit the expression of reserpine-induced oral movements. In this respect, oral movements is associated with important neuropathologies. This study investigates the effects of an acute or a repeated treatment of different doses of the GABA(B) agonist baclofen, as well as withdrawal from these treatments, on the development and/or expression of reserpine-induced vacuous chewing movements (VCM). Male mice received two injections of vehicle or of 1mg/kg reserpine separated by 48h. In the first experiment, 24h later, animals were acutely treated with vehicle or baclofen (1, 2 or 4mg/kg). In the second experiment, animals were treated with vehicle or baclofen (1 or 4mg/kg) for four consecutive days receiving a concomitant injection of 1mg/kg reserpine (or vehicle) on Days 2 and 4. Twenty-four hours later, animals received vehicle or baclofen. Thirty minutes after the last injection, they were observed for quantification of VCM and open-fieldgeneral activity. The acute administration of all the doses of baclofen abolished the manifestation of reserpine-induced VCM. Repeated treatment with 1mg/kg baclofen induced tolerance to the ability of an acute injection of this dose to reduce VCM. Treatment with baclofen (4mg/kg) did not modify spontaneous VCM. Acute administration of the highest dose induced a decrease in general motor activity and a potentiation of the reserpine-induced decrease in general activity. These results reinforce the involvement of GABAergic hypofunction in the expression of oral movements and suggest that a repeated treatment with baclofen induces compensatory changes in GABAergic transmission that can attenuate its acute property to decrease VCM.
机译:我们已经描述过,GABA模拟药物具有抑制利血平诱导的口腔运动表达的能力。在这方面,口腔运动与重要的神经病理学有关。这项研究调查了急性或反复治疗不同剂量的GABA(B)激动剂巴氯芬以及从这些治疗中退出对利血平诱导的空腹咀嚼运动(VCM)的发育和/或表达的影响。雄性小鼠接受两次注射媒介物或1mg / kg利血平,间隔48小时。在第一个实验中(24小时后),用媒介物或巴氯芬(1、2或4mg / kg)对动物进行急性治疗。在第二个实验中,动物在第2天和第4天接受媒介物或巴氯芬(1或4mg / kg)连续四天接受同时注射1mg / kg利血平(或媒介物)的治疗。二十四小时后,接受动物载体或巴氯芬。最后一次注射后30分钟,观察它们的VCM定量和开放野外活动。所有剂量的巴氯芬的急性给药消除了利血平诱导的VCM的表现。用1mg / kg巴氯芬重复治疗可引起对该剂量的急性注射降低VCM的耐受性。巴氯芬(4mg / kg)治疗未改变自发性VCM。最高剂量的急性给药引起一般运动活动的减少,利血平引起的一般活动的减少的增强。这些结果加强了GABA能功能低下在口腔运动表达中的参与,并表明用巴氯芬反复治疗可引起GABA能传递的代偿性变化,从而削弱其急性特性以降低VCM。

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