首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Protective effect of Curcumin, the active principle of turmeric (Curcuma longa) in haloperidol-induced orofacial dyskinesia and associated behavioural, biochemical and neurochemical changes in rat brain.
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Protective effect of Curcumin, the active principle of turmeric (Curcuma longa) in haloperidol-induced orofacial dyskinesia and associated behavioural, biochemical and neurochemical changes in rat brain.

机译:姜黄素,姜黄的有效成分姜黄素(姜黄)对氟哌啶醇引起的口面运动障碍以及相关的大鼠脑行为,生化和神经化学变化的保护作用。

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摘要

Tardive dyskinesia (TD) is a motor disorder of the orofacial region resulting from chronic neuroleptic treatment. A high incidence and irreversibility of this hyperkinetic disorder has been considered a major clinical issue in the treatment of schizophrenia. The molecular mechanism related to the pathophysiology of tardive dyskinesia is not completely known. Various animal studies have demonstrated an enhanced oxidative stress and increased glutamatergic transmission as well as inhibition in the glutamate uptake after the chronic administration of haloperidol. The present study investigated the effect of curcumin, an antioxidant, in haloperidol-induced tardive dyskinesia by using different behavioural (orofacial dyskinetic movements, stereotypy, locomotor activity, % retention), biochemical (lipid peroxidation, reduced glutathione levels, antioxidant enzyme levels (SOD and catalase) and neurochemical (neurotransmitter levels) parameters. Chronic administration of haloperidol (1 mg/kg i.p. for 21 days) significantly increased vacuous chewing movements (VCM's), tongue protrusions, facial jerking in rats which was dose-dependently inhibited by curcumin. Chronic administration of haloperidol also resulted in increased dopamine receptor sensitivity as evident by increased locomotor activity and stereotypy and also decreased % retention time on elevated plus maze paradigm. Pretreatment with curcumin reversed these behavioral changes. Besides, haloperidol also induced oxidative damage in all major regions of brain which was attenuated by curcumin, especially in the subcortical region containing striatum. On chronic administration of haloperidol, there was a decrease in turnover of dopamine, serotonin and norepinephrine in both cortical and subcortical regions which was again dose-dependently reversed by treatment with curcumin. The findings of the present study suggested for the involvement of free radicals in the development of neuroleptic-induced tardive dyskinesia and point to curcumin as a possible therapeutic option to treat this hyperkinetic movement disorder.
机译:迟发性运动障碍(TD)是慢性神经安定药治疗引起的口面部运动障碍。该运动亢进症的高发病率和不可逆性已被认为是精神分裂症治疗中的主要临床问题。与迟发性运动障碍的病理生理有关的分子机制尚不完全清楚。各种动物研究表明,长期服用氟哌啶醇后,氧化应激增加,谷氨酸能传递增加,谷氨酸吸收受到抑制。本研究通过使用不同的行为(面部运动障碍,刻板印象,运动功能,保留率%),生化(脂质过氧化,降低的谷胱甘肽水平,抗氧化酶水平(SOD)和过氧化氢酶)以及神经化学(神经递质水平)参数。氟哌啶醇(1 mg / kg腹腔注射,持续21天)的长期给药显着增加了大鼠的空腹咀嚼运动(VCM's),舌头突出,面部抽搐,姜黄素可剂量依赖性地抑制其空腹。长期服用氟哌啶醇还可以增强运动活性和刻板印象,从而提高多巴胺受体的敏感性,同时减少在高架迷宫范式下的保留时间,使用姜黄素预处理可以逆转这些行为改变,此外,氟哌啶醇还可以在所有主要区域诱发氧化损伤。姜黄素减弱的大脑特别是在含有纹状体的皮层下区域。氟哌啶醇的长期给药后,皮质和皮质下区域的多巴胺,5-羟色胺和去甲肾上腺素的转换减少,再次通过姜黄素剂量依赖性地逆转。本研究的发现表明,自由基参与神经安定药引起的迟发性运动障碍的发展,并指出姜黄素是治疗这种运动亢进性运动障碍的一种可能的治疗选择。

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