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出 处:《现代生物医学进展》2010年第13期2428-2431,共4页Progress in Modern Biomedicine
摘 要:目的:探讨芸香甙(Rutoside,Ru)对环孢素A(cyclosporine A,CsA)肾毒性防护作用及其机制。方法:取雄性SD大鼠20只,随机分为4组(n=5):正常对照组、Ru组、CsA模型组、CsA+Ru治疗组。CsA模型组和CsA+Ru治疗组均用CsA50mg/kg灌胃,Ru组与CsA+Ru组分别腹腔注射NS10ml/kg+Ru20mg/kg。以上各组每天给药一次,连续给药15天。各组大鼠于给药第14天后置代谢笼中收集24h尿液,测定尿Cr、尿蛋白含量。末次给药5个小时后,取血检测血清Cr、BUN含量和肾组织中丙二醛(MDA)含量、内皮素(ET)含量和超氧化物歧化酶(SOD)活性;肾组织用10%甲醛溶液固定,石蜡包埋,HE染色,光镜观察肾组织其形态学变化。结果:Ru对CsA所致的尿蛋白、BUN、Cr、肾组织MDA、ET含量的升高均有显著降低作用,并明显增加肾组织SOD活性,对CsA引起的肾小球与肾小管的病理性损伤有较好的保护作用。结论:Ru对CsA所致的肾脏毒性具有明显的保护作用。Objective:To explore the hypothesis and the mechanisms that Rutoside(Ru) may be protective against cyclosporine(CsA)-induced nephrotoxicity.Methods:Male Sprague-Dawley(SD) rats were randomly assigned into four groups of five rats each.Control group,Rutoside group,CsA group,CsA plus Rutoside group.CsA group and CsA plus Rutoside group were gived CsA(50 mg/kg) with Olive,Rutoside group and CsA plus Rutoside group were gived Rutoside(20mg/kg)with NS(10ml/kg)by Intraperitoneally.The all groups were administered once day respectively for 15 days.Twenty-four hour urines were collected at the 14th day respectively after administration to measure the content of urinary protein and urinary creatinine(UCr).The rats in all groups were anaesthetized 5 h after the last administration,Blood samples were collected to measure serum creatinine(SCr),and blood urea nitrogen(BUN).Kidneys were removed rapidly,excised and sectioned for histological analysis.Other kiney tissues were utilized for biochemical analysis.Result:Quercetin prevented urinary protein,SCr,BUN,and kidneys histological alterations.Rutoside significantly decreased malondial dehyde(MDA) and endothelin(ET) content while significantly increased,superoxide dismutase(SOD) activities of kidneys tissues in therats treated with CsA.Conclusion:Rutoside can effectively attenuate the nephrotoxicity induced by CsA.
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