Bishnoi Mahendra, Chopra Kanwaljit, Kulkarni Shrinivas K
Centre with Potential for Excellence in Biomedical Sciences, Panjab University, Chandigarh - 160 014, India.
Fundam Clin Pharmacol. 2007 Oct;21(5):521-9. doi: 10.1111/j.1472-8206.2007.00512.x.
The occurrence and irreversibility of tardive dyskinesia (TD), a motor disorder of the orofacial region, resulting from chronic neuroleptic treatment has been considered a major clinical issue in the treatment of schizophrenia. The molecular mechanism underlying the pathophysiology of TD is not completely known. Several animal studies have demonstrated an enhancement of oxidative damage and increased glutamatergic transmission after chronic administration of neuroleptics. The present study investigated the effect of rutin, an antioxidant in haloperidol-induced orofacial dyskinesia by using different behavioural (orofacial dyskinetic movements, stereotypic rearing, locomotor activity, percent 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, tongue protrusions and facial jerking in rats, which were significantly inhibited by rutin. Chronic administration of haloperidol also resulted in dopamine receptor sensitivity as evident by a well-shaped response (initial decrease followed by increase) in locomotor activity and stereotypic rearing and also decreased percent retention time on elevated plus maze paradigm. Pretreatment with rutin reversed these behavioural changes. Besides, haloperidol also induced oxidative damage in all regions of brain which was prevented by rutin, especially in the subcortical region containing striatum. Although turnover of dopamine and noradrenaline decreased in both cortical and subcortical regions after chronic administration of haloperidol, it was significantly reversed by high-dose rutin treatment. The findings of the present study suggested the involvement of free radicals in the development of neuroleptic-induced orofacial dyskinesia, a putative model of TD, and rutin as a possible therapeutic option to treat this hyperkinetic movement disorder.
迟发性运动障碍(TD)是一种口面部区域的运动障碍,由长期使用抗精神病药物引起,其发生及不可逆性被认为是精神分裂症治疗中的一个主要临床问题。TD病理生理学的分子机制尚未完全明确。多项动物研究表明,长期使用抗精神病药物后,氧化损伤增强,谷氨酸能传递增加。本研究通过使用不同的行为学(口面部运动障碍、刻板饲养、运动活性、记忆保留率)、生物化学(脂质过氧化、还原型谷胱甘肽水平、抗氧化酶水平(超氧化物歧化酶和过氧化氢酶))和神经化学(神经递质水平)参数,研究了芦丁(一种抗氧化剂)对氟哌啶醇诱导的口面部运动障碍的影响。长期给予氟哌啶醇(1mg/kg腹腔注射,共21天)显著增加了大鼠的空嚼运动、伸舌和面部抽搐,而芦丁可显著抑制这些症状。长期给予氟哌啶醇还导致多巴胺受体敏感性增加,表现为运动活性和刻板饲养中出现典型反应(先下降后上升),以及高架十字迷宫实验中记忆保留时间百分比降低。芦丁预处理可逆转这些行为变化。此外,氟哌啶醇还在脑的所有区域诱导了氧化损伤,而芦丁可预防这种损伤,尤其是在含有纹状体的皮层下区域。虽然长期给予氟哌啶醇后,皮层和皮层下区域的多巴胺和去甲肾上腺素周转率均降低,但高剂量芦丁治疗可显著逆转这一现象。本研究结果表明,自由基参与了抗精神病药物诱导的口面部运动障碍(一种TD的假定模型)的发生,芦丁可能是治疗这种运动亢进性疾病的一种治疗选择。