Castro Juliana P M V, Frussa-Filho Roberto, Fukushiro Daniela F, Silva Regina H, Medrano Wladimir A, Ribeiro Rosana de A, Abílio Vanessa C
Department of Pharmacology, Escola Paulista de Medicina/UNIFESP, São Paulo, Brazil.
Brain Res Bull. 2006 Feb 15;68(6):436-41. doi: 10.1016/j.brainresbull.2005.09.019. Epub 2005 Nov 14.
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 48 h. In the first experiment, 24h later, animals were acutely treated with vehicle or baclofen (1, 2 or 4 mg/kg). In the second experiment, animals were treated with vehicle or baclofen (1 or 4 mg/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-field general 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 (4 mg/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.
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相关。本研究调查了不同剂量的GABA(B)激动剂巴氯芬急性或重复给药,以及这些治疗停药后,对利血平诱导的空嚼运动(VCM)的发生和/或表达的影响。雄性小鼠在间隔48小时的情况下接受两次注射溶剂或1mg/kg利血平。在第一个实验中,24小时后,动物被急性给予溶剂或巴氯芬(1、2或4mg/kg)。在第二个实验中,动物连续四天接受溶剂或巴氯芬(1或4mg/kg)治疗,在第2天和第4天同时注射1mg/kg利血平(或溶剂)。24小时后,动物接受溶剂或巴氯芬。最后一次注射后30分钟,观察它们以量化VCM和旷场一般活动。所有剂量的巴氯芬急性给药均消除了利血平诱导的VCM的表现。用1mg/kg巴氯芬重复治疗诱导对该剂量急性注射减少VCM能力的耐受性。用巴氯芬(4mg/kg)治疗未改变自发VCM。最高剂量的急性给药导致一般运动活动减少,并增强了利血平诱导的一般活动减少。这些结果加强了GABA能功能减退在口腔运动表达中的作用,并表明用巴氯芬重复治疗诱导GABA能传递的代偿性变化,这可以减弱其急性减少VCM的特性。