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首页> 外文期刊>Behavioural Brain Research: An International Journal >Ameliorating effect of piperine on behavioral abnormalities and oxidative markers in sodium valproate induced autism in BALB/C mice
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Ameliorating effect of piperine on behavioral abnormalities and oxidative markers in sodium valproate induced autism in BALB/C mice

机译:哌啶对Balb / C小鼠钠丙酸钠诱导自闭症中行为异常和氧化标志物的改善作用

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Post natal exposure to VPA (valproic acid) in mice induces behavioral deficits, abnormal sensitivity to sensory stimuli and self-injurious behavior, observed in autism. Piperine has been reported to have protective effect on brain. The present study aimed at evaluating effect of piperine on VPA induced neurobehavioral and biochemical alterations in BALB/c mice. Young BALB/c mice 13 days old were procured from five different litters and segregated into five groups (n = 6; 3 male, 3 female) i.e., Group I served as control group, received physiological saline on PND (Post natal day) 14 & Tween 80 p.o. from PND13-40. Group II served as normal treated group and received piperine (20 mg/kg p.o.) from PND 13-40 and saline s.c. on PND 14. Group III served as valproate treated group received VPA (400 mg/kg s.c.) on PND 14 and Tween 80 p.o. from PND 13-40. Group IV & V served as disease treated group received VPA (400 mg/kg s.c.) on PND 14 & piperine (5 & 20 mg/kg p.o.) from PND 13-40 respectively. BALB/c mice pups were subjected to behavioral testing to assess motor skill development, nociceptive response, locomotion, anxiety, and cognition on various postnatal days up to PND 40. At the end of behavioral evaluation, mice were sacrificed; brain was isolated for biochemical estimations (serotonin, glutathione, MDA and nitric oxide) and histopathological examination. Our study revealed that treatment with piperine significantly improved behavioral alterations, lowered oxidative stress markers, and restored histoarchitecture of cerebellum. This ameliorating effect of piperine is attributed to its anti-oxidant activity, cognition enhancing and neuroprotective activity. (C) 2014 Elsevier B.V. All rights reserved.
机译:在自闭症中,在小鼠中对VPA(丙戊酸)的产程缺乏,对感官刺激和自我伤害行为的异常敏感性,观察到。据报道,哌啶对脑具有保护作用。本研究旨在评估哌啶对VPA诱导的BALB / C小鼠诱导的神经干扰和生化改变的影响。 13天大的Balb / C小鼠从五个不同的窝水中采购并分为五组(n = 6; 3只男性,3名女性)即,我作为对照组的组,接受了PND的生理盐水(产前日期)14 &Tween 80 PO来自PND13-40。 II族作为正常治疗组和接受PND 13-40和盐水的哌啶(20mg / kg p.o.)。关于PND 14. III组致丙戊酸治疗组,在PND 14和TWEEN 80 P.O上获得VPA(400mg / kg S.C.)。从PND 13-40。 IV&V分别用作疾病治疗组的PND 14和Pliperine(5&20mg / kg P.O)的疾病治疗组分别来自PND 13-40。对BALB / C小鼠幼犬进行行为测试,以评估各种后期的运动技能,伤害反应,焦虑,焦虑和认知。在行为评估结束时,处死小鼠;将脑分离生化估计(血清素,谷胱甘肽,MDA和一氧化氮)和组织病理学检查。我们的研究表明,用哌啶治疗显着提高了行为改变,降低了氧化应激标记物,并恢复了小脑组织建筑。这种哌啶的改善效果归因于其抗氧化活性,认知增强和神经保护活性。 (c)2014 Elsevier B.v.保留所有权利。

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