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| 苦参素降低大鼠肾脏缺血-再灌注损伤 | |
| 引用本文： | 贾昌盛,孙建军,李美德,黎金浓,陈瑞琦,曾明,廖联明.苦参素降低大鼠肾脏缺血-再灌注损伤[J].基础医学与临床,2012,32(8):943-947. |
| 作者姓名： | 贾昌盛 孙建军 李美德 黎金浓 陈瑞琦 曾明 廖联明 |
| 作者单位： | 1. 安徽医科大学研究生院,安徽合肥230032;北京军区总医院药理科,北京100700 2. 南京军区福州总医院476临床部,福建福州,350002 3. 福建中医药大学中西医结合研究院,福建福州,350108 |
| 摘 要： | 目的观察苦参素的抗大鼠肾缺血再灌注损伤的作用并从抗氧化方面探讨其机制。方法用双肾肾蒂夹闭45 min建立IRI模型,将SD大鼠随机分为假手术组(sham);缺血再灌注组(I/R);苦参素治疗组(oxymatrine+I/R)。苦参素治疗组又分为高、中和低3个剂量组,在缺血再灌注前,连续7 d经腹腔注射。用自动生化仪测定血清肌酐(Scr)和尿素氮(BUN)水平,观察苦参素对肾缺血再灌注的保护作用及确定最优剂量;以最优剂量干预用分光分析法测定肾组织丙二醛(MDA)、谷胱甘肽过氧化物酶(GSH-Px)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)水平。结果不同剂量组均能明显减轻肾脏IRI的病理形态学改变,改善肾功能。与I/R组相比,再灌注72 h后,MDA水平,血清肌酐(Scr)和尿素氮(BUN)水平明显降低(P<0.05);苦参素治疗组的CAT、T-SOD、GSH-Px活性改善明显(P<0.05)。苦参素无体外抗氧化作用。结论苦参素对大鼠肾缺血再灌注损伤具有保护作用,作用机制可能与调控机体的抗氧化系统有关。 |
| 关 键 词： | 苦参素 肾脏 缺血再灌注损伤 |
Oxymatrine attenuates ischemia/reperfusion injury in rat kidneys |
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| JIA Chang-sheng , SUN Jian-jun , LI Mei-de , LI Jin-nong , CHEN Rui-qi , ZENG Ming , LIAO Lian-ming.Oxymatrine attenuates ischemia/reperfusion injury in rat kidneys[J].Basic Medical Sciences and Clinics,2012,32(8):943-947. | |
| Authors: | JIA Chang-sheng SUN Jian-jun LI Mei-de LI Jin-nong CHEN Rui-qi ZENG Ming LIAO Lian-ming |
| Affiliation: | 1.Graduate School,Anhui Medical University,Hefei 230032;2.the 476th Clinical Department,Fuzhou General Hospital of Nanjing Military Command,Fuzhou 350002;3.Academy of Integrative Medicine,Fujian University of Traditional Chinese Medicine, Fuzhou 350108;4.Dept.Pharmacology,the Military General Hospital of Beijing PLA,Beijing 100700,China) |
| Abstract: | Objective Renal ischemia followed by reperfusion leads to acute renal failure,which is a complex pathophysiologic process involving hypoxia and free radical(FR) damage.We aimed to investigate the effect of oxymatrine on kidney ischemia/reperfusion(I/R) injury and the antioxidant effects of oxymatrine in rats.MethodsSD rats were randomly divided into 5 groups(I/R group,sham operation group and oxymatrine treatment groups).Rats in the I/R group were subjected to bilateral renal ischemia for 45 min and followed by reperfusion.Rats in the oxymatrine treatment groups received oxymatrine intraperitoneally(i.p.) at 3 different doses before I/R for 7 days.In some experiments,rats were killed and kidney function,tissue catalase(CAT),malondialdehyde(MDA) levels,superoxide dismutase(SOD) and glutathione peroxidase(GSH-Px) activities were determined.ResultsOxymatrine significantly prevented I/R-induced kidney injury as indicated by decreased serum creatinine(Scr) and blood urea nitrogen(BUN) levels compared to I/R group(P<0.05).Reduction of tissue CAT,SOD and GSH-Px activities after I/R were significantly improved by oxymatrine(P<0.05).Treatment with oxymatrine also resulted in significant reduction in tissue MDA that was increased by renal I/R injury(P<0.05).Conclusions Based on our results,it could therefore be concluded that oxymatrine protects the kidneys against I/R injury at least partly via its antioxidant effects. |
| Keywords: | oxymatrine kidney ischemia-reperfusion injury |
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