摘要
背景:衰老大鼠静脉注射脂多糖后能导致肺损伤,进而发现随着肺损伤的进展,影响肾功能。银杏叶提取物具有一定的清除自由基、改善血液流变学和保护血管内皮细胞等功能。目的:研究人工衰老大鼠肺损伤后是否发生肾功能不全,以验证老年多器官功能不全的肺启动机制,并观察银杏叶提取物对其是否有保护作用。设计:以实验动物为观察对象的随机对照的实验。单位:中国协和医科大学基础医学研究所病理生理学系。材料:实验于2001-05/2003-01在中国协和医科大学基础医学研究所病理生理学系实验室完成。选用36只Wistar雄性大鼠。方法:给大鼠每天1次经腹腔注入D-半乳糖(50mg/kg),连续6周,复制衰老动物模型,再随机分为3组:对照组(静脉注射生理盐水);脂多糖组(静脉注射脂多糖,5mg/kg);银杏叶提取物+脂多糖组(注射脂多糖前7d开始,每天银杏叶提取物灌胃1次,31mg/kg)。各组大鼠在给生理盐水或脂多糖后2h或6h取血和肺、肾组织。主要观察指标:用比色法测定血中肌酐、尿素氮含量;血、肺、肾组织中丙二醛、NO2-/NO3-含量及谷胱甘肽过氧化物酶及Na+-K+-ATP酶活性的测定。结果:衰老大鼠在注射脂多糖后2,6h时已形成急性肺损伤。注射脂多糖后2h血中肌酐及尿素氮含量无明显升高,而6h时均显著升高,分别为(94.7±10.3)μmol/L,(11.4±1.9)mmol/L。在注射脂多糖后2h,血和肺组织中丙二醛犤(22.5±2.6)nmol/L,(25.8±2.9)μmol/g犦和NO2-/NO3-含量犤(58.5±6.8)mmol/L,(34.6±3.8)μmol/g犦均显著升高,而谷胱甘肽过氧化物酶犤(355.1±45.0)μkat/g犦及Na+-K+-ATP酶犤(886.3±97.2)nkat/g犦下降。上述指标的变化持续至观察的6h。而肾组织中上述指标仅在注射脂多糖后6h才有显著性变化。银杏叶提取物可显著缓解上述指标的变化。结论:脂多糖所致衰老大鼠的肺损伤可进一步诱导肾功能受损。银杏叶提取物对脂多糖诱发的�
BACKGROUND：Lung injury be induced after injection of lipopolysaccharide（LPS） into the vein of aging rats,and with the development of lung injury,the kidney function can be influenced. Ginkgo biloba extract（GBE） has some effects such as clearing the free radicals, improving hemorrheology,protecting the vascular endothelial cells and so OBJECTIVE：To investigate whether renal function damage is induced by acute lung injury（ALl） in aging rats so as to support the hypothesis that lung is the start-up organ in multiple organ dysfunction syndrome in the elderly and the protective effect of GBE on it. DESIGN：Randomized controlled experimental trial based on the experimental animals. SETTING：Laboratory of Department of Pathophysiology,Institute of Basic Medical Science,Peking Union Medical College. MATERIALS：The study has been completed from May 2001 to January 2003 in the Laboratory of Department of Pathophysiology,Institute of Basic Medical Science,Peking Union Medical College.Thirty-six Wistar male rats were involved. INTERVENTIONS：For reproducing the mimic aging rats models,the rats were injected intraperitoneally,D-gal 50 mg/kg,once a day,for 6 weeks totally,and randomly divided into 3 groups, namely： ①control group（saline ,intravenous injection）;② LPS group（ LPS,5 mg/kg intravenous injection） ③ GBE＋LPS group （GBE was used 7 days prior to LPS,31 mg/kg ,once a day）.Samples（blood,lung and kidney tissue） were collected at 2 or 6 hours after LPS or saline administration. MAIN OUTCOME MEASURES：Contents of creatinine（Cr）,bloed urea nitrogen （BUN）,lactic acid （LA）,NO （its metabolite is NO2^-/NO3^-） andmethane dicarboxylic aldehyde（MDA）;and activities of glutathione peROxi-dase（GSH-Px） and Na^＋-K^＋-ATPase were measured. RESULTS：Compared with control group,there was obviously ALl at 2 or 6 hours after LPS administration.Cr [（94.7±10.3） μmoL/L ]and BUN[（11.4±l.9）mmol/L]contents in blood were increased significantly unti 16 hours after
出处
《中国临床康复》
CSCD
北大核心
2005年第27期239-241,共3页
Chinese Journal of Clinical Rehabilitation
基金
国家重点基础研究规划项目
(973)基金资助(G2000057004)
国家自然科学基金资助(30170400)~~
