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The neuroprotective effect of lithium against high dose methylphenidate: Possible role of BDNF

机译:锂对大剂量哌醋甲酯的神经保护作用:BDNF的可能作用

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Methylphenidate (MPH) is a neural stimulant with unclear neurochemical and behavioral effects. Lithium is a neuroprotective agent in use clinically for the management of manic-depressive and other neurodegenerative disorders. This study investigated the protective effect of lithium on MPH-induced oxidative stress, anxiety, depression and cognition impairment. Forty-eight adult male rats were divided randomly and equally into 6 groups. Treatment groups were received MPH (10 mg/kg) and various doses of lithium (75, 150 and 300 mg/kg) simultaneously and also lithium (150 mg/kg) alone for 21 days. Elevated Plus Maze and Forced Swim Test were used to determine the level of anxiety and depression in animals. Morris Water Maze was used to evaluate spatial learning and memory. The hippocampi of rats were isolated and the level and activity of oxidative, anti-oxidant and inflammatory factors were measured. Also brain derived neurotropic factor expression level was measured by RT-PCR and western blotting. MPH (10 mg/kg) caused behaviors indicative of anxiety and depression-like phenotypes in EPM and FST and cognition impairment in MWM. While lithium in all mentioned doses inhibited these effects. Treatment with MPH significantly increased lipid peroxidation, mitochondrial GSH content and IL-1 beta and TNF-alpha levels in isolated hippocampal cells. Moreover superoxide dismutase and glutathione peroxidase activities and BDNF expression remarkably decreased. Various doses of lithium attenuated these effects and significantly mitigated MPH-induced oxidative damage, inflammation and increased BDNF expression level. Lithium has the potential to act as a neuroprotective agent against MPH induced toxicity in rat brain and this might be mediated by BDNF expression in hippocampus of rats. (C) 2016 Elsevier B.V. All rights reserved.
机译:哌醋甲酯(MPH)是一种神经兴奋剂,其神经化学和行为作用尚不清楚。锂是一种临床上用于治疗躁狂抑郁症和其他神经退行性疾病的神经保护剂。这项研究调查了锂对MPH诱导的氧化应激,焦虑,抑郁和认知障碍的保护作用。将48只成年雄性大鼠随机分为6组。治疗组同时接受MPH(10 mg / kg)和各种剂量的锂(75、150和300 mg / kg),还单独接受锂(150 mg / kg),持续21天。高架迷宫和强迫游泳测试用于确定动物的焦虑和抑郁水平。莫里斯水迷宫被用来评估空间学习和记忆。分离大鼠海马,测定其氧化,抗氧化和炎性因子的水平和活性。还通过RT-PCR和蛋白质印迹法测量了脑源性神经营养因子的表达水平。 MPH(10 mg / kg)引起的行为表明了EPM和FST中的焦虑和抑郁样表型以及MWM中的认知障碍。尽管所有提及剂量的锂均抑制了这些作用。 MPH的治疗显着增加了离体海马细胞中的脂质过氧化,线粒体GSH含量以及IL-1β和TNF-α水平。此外,超氧化物歧化酶和谷胱甘肽过氧化物酶活性和BDNF表达显着下降。各种剂量的锂减弱了这些作用,并显着减轻了MPH诱导的氧化损伤,炎症和BDNF表达水平的提高。锂具有作为抗MPH诱导的大鼠脑毒性的神经保护剂的潜力,这可能是由大鼠海马中的BDNF表达介导的。 (C)2016 Elsevier B.V.保留所有权利。

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