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决明子提取物对小鼠实验性晶状体氧化应激状态的影响
引用本文:黄晓丹,郑荣波,谭蕊蓉,和海龙,李维熙,李怡芳,何蓉蓉,栗原博.决明子提取物对小鼠实验性晶状体氧化应激状态的影响[J].中药新药与临床药理,2012,23(2):167-170.
作者姓名:黄晓丹  郑荣波  谭蕊蓉  和海龙  李维熙  李怡芳  何蓉蓉  栗原博
作者单位:1. 广州王老吉药业股份有限公司,广州510450;暨南大学中药及天然药物研究所,广州510632
2. 广州王老吉药业股份有限公司,广州,510450
3. 暨南大学中药及天然药物研究所,广州,510632
4. 暨南大学中药及天然药物研究所,广州510632;云南中医学院中药学院,昆明650500
摘    要:目的研究决明子提取物对溴酸钾(KBrO3)/伤寒沙门氏菌脂多糖(LPS)诱发小鼠晶状体氧化应激状态的改善作用。方法小鼠尾静脉注射2 mg.kg-1LPS,同时腹腔注射200 mg.kg-1KBrO3制备小鼠晶状体氧化应激模型。50,150和450 mg.kg-1决明子提取物在LPS/KBrO3给药同时及3 h前分别灌胃2次,对照组灌胃同体积水溶液。LPS/KBrO3给药6 h后,乙醚麻醉条件下采取小鼠晶状体测定抗氧化能力指标。结果单独腹腔注射200 mg.kg-1KBrO3或尾静脉注射2 mg.kg-1LPS 6 h后,小鼠晶状体组织内谷胱甘肽(GSH)水平均有所降低,而当KBrO3并用LPS时则显著诱发小鼠晶状体氧化应激状态。50,150及450 mg.kg-1决明子提取物灌胃给药能够有效的改善因KBrO3/LPS诱导小鼠晶状体组织内GSH含量的减少、提高抗氧化能力指数(ORAC)和降低丙二醛(MDA)水平,并呈一定的量效关系。结论决明子提取物可以改善小鼠晶状体内的过氧化状态,其作用机制可能是通过清除自由基和抑制脂质过氧化过程实现的。

关 键 词:决明子  晶状体  溴酸钾  内毒素  氧化应激损伤

Effects of Semen Cassiae Extract on Oxidative Stress Status of Mice Lens
HUANG Xiaodan , ZHENG Rongbo , TAN Ruirong , HE Hailong , LI Weixi , LI Yifang , HE Rongrong , KURIHARA Hiroshi.Effects of Semen Cassiae Extract on Oxidative Stress Status of Mice Lens[J].Traditional Chinese Drug Research & Clinical Pharmacology,2012,23(2):167-170.
Authors:HUANG Xiaodan  ZHENG Rongbo  TAN Ruirong  HE Hailong  LI Weixi  LI Yifang  HE Rongrong  KURIHARA Hiroshi
Institution:HUANG Xiaodan1,2,ZHENG Rongbo1,TAN Ruirong2,HE Hailong1,LI Weixi2,3,LI Yifang2,HE Rongrong2,KURIHARA Hiroshi2(1.Guangzhou Wanglaoji Pharmaceutical Company Limited,Guangzhou 510450,China;2.Institute of Traditional Chinese Medicine & Natural Products,Jinan University,Guangzhou 510632,China;3.College of Chinese Materia Medica,Yunnan College of Traditional Chinese Medicine,Kunming 650500,China)
Abstract:Objective To investigate the protective effects of Semen Cassiae extract(SCE) on oxidative status of mice lens induced by kalium bromicum/ typhoid Bacillus lipopolysaccharide(KBrO3 /LPS).Methods The mice lens oxidative stress model was established by injection of LPS(2 mg·kg-1) into the caudal vein and synchronously intraperitoneal injection of KBrO3(200 mg·kg-1) in Kuming mice.Low,moderate and high dose of SCE(50,150 and 450 mg·kg-1) were given intragastrically to mice for twice,3 hours early before and at the same time of KBrO3 / LPS administration,respectively.The control groups were given the same volume of water.Mice lens were taken out 6 hours after KBrO3 / LPS injection to evaluate antioxidant capacity indexes.Results Intraperitoneal injection of KBrO3(200 mg·kg-1) or injection of LPS(2 mg·kg-1) into the caudal vein alone decreased glutathione(GSH) content in mice lens 6 hours after administration,but the combination of KBrO3 and LPS induced the oxidative stress status of mice lens.The administration of SCE could effectively improve the reduction of GSH content,elevate the oxygen-radical absorbing capality(ORAC) a nd decrease MDA content,the effect was in dose-dependent manner.Conclusion SCE could improve oxidative stress status of mice lens induced by KBrO3 /LPS.The mechanism may be related to the elimination of free radicals and inhibition of lipid peroxidation.
Keywords:Semen Cassiae extract  Lens  Kalium Bromicum  Endotoxin  Oxidative Damage
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