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作 者:查渝[1] 王锦权[1] 刘宝[1] 陶晓根[1] 赵劲松[1] 杜庆[1]
机构地区:[1]安徽医科大学附属省立医院安徽省立医院ICU,合肥230001
出 处:《中国临床保健杂志》2009年第3期280-282,共3页Chinese Journal of Clinical Healthcare
基 金:安徽省自然科学基金资助项目(KJ2007B214)
摘 要:目的探讨川芎嗪(TMP)对腹腔间隔室综合征(ACS)致急性肾损伤的保护作用机制。方法将60只新西兰白兔随机分成5组,每组12只;对照组(C组)、ACS持续2 h组(A2组)和4 h组(A4组),TMP干预2 h组(T2组)和4 h组(T4组)。腹腔灌注氮气制备ACS兔实验动物模型;TMP干预组在实验前1h给予TMP 60 mg/kg静脉注射。实验结束后采血并处死动物,检测相关观察指标。结果ACS兔实验动物模型随着血内毒素浓度升高,血清肌酐(Cr)、尿素氮(BUN)、半胱氨酸蛋白酶抑制剂C(Cys C)和尿Cys C也升高,呈正相关(均P<0.01),尿量则减少,呈负相关(P<0.01)。与A2组比较,T2组实验动物血清Cr、BUN、Cys C、内毒素较低(均P<0.01),尿量、尿Cys C升高(均P<0.01)。与A4组比较,T4组实验动物血清内毒素升高(P<0.01)。结论TMP早期干预可降低ACS实验动物血清内毒素浓度,改善肾小球滤过率和肾小管重吸收功能,对ACS造成的急性肾损伤具有保护作用。Objective To study the protective effect and mechanism of tetramethylpyrazine (TMP) on acute kidney injury caused by abdominal compartment syndrome (ACS). Methods 60 New Zealand rabbits were randomly divided into 5 groups, i. e. normal control ( C), ACS 2 hours ( A2 ), ACS 4 hours ( A4), TMP therapy ACS 2 hours (T2) and TMP therapy ACS 4 hours (T4) ,with 12 rabbits in each group. ACS model rabbits were made by injecting nitrogen gas into abdominal cavity. 60mg/kg TMP was administered intravenously into the rabbits of Group T2 and T4 on 1 hour before ACS. Serum creatinine (Cr) ,urea nitrogen (BUN) ,Cystatin C (Cys C) ,urinary Cys C and serum endotoxin were detected respectively, and then the rabbits were killed after the experiment. Results In the ACS model rabbits, serum Cr, BUN, Cys C and urinary Cys C levels were all positively correlated with serum endotoxin level (P 〈 0.01 ). Between urine volume each hour and serum endotoxin level was negatively correlated ( P 〈 0.01 ). Compared with A2 group, serum Cr, BUN, Cys C and endotoxin levels were higher ( P 〈 0.01 ), and urine volume each hour and urinary Cys C were lower (P 〈 0.01 )in T2 group. Serum endotoxin level was higher in T4 group than in A4 group (P 〈 0.01 ). Conclusion Early intervention of TMP can protect kidney in the rabbit with ACS early by decreasing serum endotoxin level and improving the function of glomerular filtration and renal tubular reabsorption.
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