姜黄醇提物对抗溴氰菊酯中毒雄性大鼠神经毒性作用的评价。
The Estimation of the Anti-neurotoxic Effect of Costus Ethanolic Extract against Bifenthrin-Intoxication in Male Rats.
出版信息
Pak J Biol Sci. 2021 Jan;24(1):112-121. doi: 10.3923/pjbs.2021.112.121.
BACKGROUND AND OBJECTIVE
Pyrethroidsare a group of synthetic pesticides similar to the natural pesticide pyrethrum, which is produced by chrysanthemum flowers. Bifenthrin is one of the pyrethroids that are widely used pesticide in households and to control crop vectors. The main goal of this work was to investigate the possible ameliorating effect of Costus Ethanolic Extract (CEE) against neurotoxicity induced by bifenthrin in adult-male rats.
MATERIALS AND METHODS
Rats were arranged randomly to 4 groups (8 rats each) as next. Group 1) control rats orally received 0.5 mL water for consecutive 30 days; group 2) healthy rats orally received CEE (200 mg kg) for consecutive thirty days; group 3) rats treated orally with 7 mg kg-1 day-1 bifenthrin for consecutive 30 days and group 4) included rats treated with bifenthrin for consecutive 30 days followed by administration with CEE another consecutive 30 days.
RESULTS
The results showed that CEE succeeded to decline the neurotoxicity-induced by bifenthrin; this was evidenced by the significant reduction in TNF-α, IL- 1β, MDA and nitric oxide levels in cortex, hippocampus and striatum concomitant with marked improvement in the values of GSH, dopamine, serotonin, AChE-ase, SOD, GPx and catalase that were diminished by bifenthrin intoxication. CEE improved also cognitive impairment and the deficits in motor coordination induced by bifenthrin.
CONCLUSION
CEE was found successful, to a great extent, to counteract the bifenthrin-induced brain oxidative stress and neurochemical deteriorations and possesses a protective potential against brain-induced neurotoxicity. Therefore, it may be a promising supplement for the amelioration of BF-neurotoxicity.
背景与目的
拟除虫菊酯是一组类似于天然除虫菊酯的合成杀虫剂,天然除虫菊酯由菊花产生。联苯菊酯是一种广泛应用于家庭和控制作物传播媒介的拟除虫菊酯。这项工作的主要目的是研究 Costus 乙醇提取物 (CEE) 对抗联苯菊酯诱导的成年雄性大鼠神经毒性的可能改善作用。
材料与方法
大鼠随机分为 4 组(每组 8 只):第 1 组)对照组大鼠连续 30 天口服 0.5mL 水;第 2 组)健康大鼠连续 30 天口服 CEE(200mg/kg);第 3 组)大鼠连续 30 天每天口服 7mg/kg-1 联苯菊酯,第 4 组)包括连续 30 天口服联苯菊酯后再连续 30 天给予 CEE。
结果
结果表明,CEE 成功降低了联苯菊酯引起的神经毒性;这表现在皮质、海马和纹状体中 TNF-α、IL-1β、MDA 和一氧化氮水平的显著降低,同时联苯菊酯中毒引起的 GSH、多巴胺、血清素、AChE-ase、SOD、GPx 和过氧化氢酶水平显著改善。CEE 还改善了由联苯菊酯引起的认知障碍和运动协调缺陷。
结论
CEE 在很大程度上成功地对抗了联苯菊酯引起的大脑氧化应激和神经化学恶化,具有对抗大脑引起的神经毒性的保护潜力。因此,它可能是改善 BF 神经毒性的有前途的补充剂。