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评价藏菖蒲对氟哌啶醇诱导的大鼠僵住症的解毒和抗氧化潜力。

Evaluation of toxicological and antioxidant potential of Nardostachys jatamansi in reversing haloperidol-induced catalepsy in rats.

机构信息

Department of Pharmacology, and Toxicology, C L Baid Metha, College of Pharmacy, Jyothi Nagar, Thoraipakkam, Chennai, Tamil Nadu, India.

出版信息

Int J Gen Med. 2010 May 26;3:127-36. doi: 10.2147/ijgm.s9156.

Abstract

An aqueous root extract from Nardostachys jatamansi was investigated for its antioxidant and anticataleptic effects in the haloperidol-induced catalepsy rat model of the disease by measuring various behavioral and biochemical parameters. Catalepsy was induced by administration of haloperidol (1 mg/kg, ip) in male albino rats. A significant (P < 0.01) reduction in the cataleptic scores were observed in all the drug-treated groups as compared to the haloperidol-treated group; with maximum reduction observed in the Nardostachys jatamansi (250 and 500 mg/kg body weight) administered group. To estimate biochemical parameters: the generation of thiobarbituric acid reactive substances (TBARS); reduced glutathione (GSH) content and glutathione-dependent enzymes; catalase; and superoxide dismutase (SOD), in the brain were assessed. Haloperidol administration increased generation of TBARS and significantly reduced GSH, which were restored to near normal level with the Nardostachys jatamansi treatment. Catalase and SOD levels were also increased to normal levels, having been reduced significantly by haloperidol administration. Our findings of behavioral studies and biochemical estimations show that Nardostachys jatamansi reversed the haloperidol-induced catalepsy in rats. We conclude that the antioxidant potential has contributed to the reduction in the oxidative stress and catalepsy induced by haloperidol administration.

摘要

从甘松香中提取的水性根提取物通过测量各种行为和生化参数,研究了其在抗精神病药引起的僵住大鼠模型中的抗氧化和抗僵住作用。通过给予雄性白化大鼠(1 mg/kg,ip)氟哌啶醇来诱导僵住。与氟哌啶醇处理组相比,所有药物处理组的僵住评分均显著降低(P < 0.01);甘松香(250 和 500 mg/kg 体重)给药组的降低幅度最大。为了评估生化参数:在大脑中评估了硫代巴比妥酸反应物质(TBARS)的生成;还原型谷胱甘肽(GSH)含量和谷胱甘肽依赖性酶;过氧化氢酶;和超氧化物歧化酶(SOD)。氟哌啶醇给药增加了 TBARS 的生成,并显著降低了 GSH,而甘松香处理可将其恢复到接近正常水平。过氧化氢酶和 SOD 水平也升高至正常水平,氟哌啶醇给药显著降低了它们的水平。我们的行为研究和生化评估结果表明,甘松香逆转了大鼠的氟哌啶醇引起的僵住。我们得出结论,抗氧化潜力有助于减少氟哌啶醇给药引起的氧化应激和僵住。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55ad/2880350/12e851dfecd9/ijgm-3-127f1.jpg

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