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抑肽酶可改善肾功能,并减少肾脏缺血再灌注后的肾小管细胞凋亡及促凋亡信号。

Aprotinin improves kidney function and decreases tubular cell apoptosis and proapoptotic signaling after renal ischemia-reperfusion.

作者信息

Kher Ajay, Meldrum Kirstan K, Hile Karen L, Wang Meijing, Tsai Ben M, Turrentine Mark W, Brown John W, Meldrum Daniel R

机构信息

Department of Surgery, Indiana University Medical Center, Indianapolis, Ind, USA.

出版信息

J Thorac Cardiovasc Surg. 2005 Sep;130(3):662-9. doi: 10.1016/j.jtcvs.2005.02.035.

Abstract

OBJECTIVE

The purpose of the study was to determine the effects of aprotinin on (1) renal function, (2) apoptosis and apoptotic signaling, and (3) the inflammatory response of the kidney after ischemia-reperfusion injury.

METHODS

Male rats underwent a sham procedure or left renal ischemia for 1 hour. Rats were divided into three groups and received no reperfusion, reperfusion for 1 hour, or reperfusion for 24 hours. The animals undergoing ischemia received saline solution alone or aprotinin (60,000 kIU/kg). At the end of the experiment, a sample for serum creatinine was taken and the left kidney was harvested. The kidney was analyzed for expression of tumor necrosis factor alpha, interleukin 1beta, and interleukin 6 (enzyme-linked immunosorbent assay and reverse transcriptase-polymerase chain reaction) and activation of p38 mitogen-activated protein kinase, caspase 3, and caspase 8 (Western blot). The kidney was assessed for apoptosis with enzyme-linked immunosorbent assay and by terminal deoxynucleotidyl transferase biotin-deoxyuridine triphosphate nick-end labeling staining of tissue slides.

RESULTS

Aprotinin significantly decreased the rise in serum creatinine and apoptosis caused by ischemia-reperfusion. Aprotinin significantly reduced interleukin 1 and 6 messenger RNA production and showed a trend toward reducing tumor necrosis factor messenger RNA production after ischemia. Aprotinin also significantly reduced caspase 8 activation and showed a trend toward decreasing p38 mitogen-activated protein kinase activation after 1 hour of reperfusion.

CONCLUSION

These results suggest that aprotinin provides protection from renal ischemia-reperfusion injury. They also suggest that aprotinin may do so by affecting apoptotic signaling and inflammatory cytokine production. Aprotinin is a potential therapeutic measure in clinical situations where renal ischemia-reperfusion injury can be anticipated, provided adequate heparinization is possible.

摘要

目的

本研究旨在确定抑肽酶对(1)肾功能、(2)细胞凋亡及凋亡信号传导,以及(3)肾脏缺血再灌注损伤后炎症反应的影响。

方法

雄性大鼠接受假手术或左肾缺血1小时。大鼠被分为三组,分别接受无再灌注、1小时再灌注或24小时再灌注。经历缺血的动物单独接受生理盐水或抑肽酶(60,000 kIU/kg)。实验结束时,采集血清肌酐样本并摘取左肾。对肾脏进行肿瘤坏死因子α、白细胞介素1β和白细胞介素6表达的分析(酶联免疫吸附测定和逆转录聚合酶链反应)以及p38丝裂原活化蛋白激酶、半胱天冬酶3和半胱天冬酶8激活情况的分析(蛋白质印迹法)。通过酶联免疫吸附测定和组织切片的末端脱氧核苷酸转移酶生物素 - 脱氧尿苷三磷酸缺口末端标记染色评估肾脏的细胞凋亡情况。

结果

抑肽酶显著降低了缺血再灌注引起的血清肌酐升高和细胞凋亡。抑肽酶显著降低了白细胞介素1和6信使核糖核酸的产生,并且在缺血后显示出降低肿瘤坏死因子信使核糖核酸产生的趋势。抑肽酶还显著降低了半胱天冬酶8的激活,并且在再灌注1小时后显示出降低p38丝裂原活化蛋白激酶激活的趋势。

结论

这些结果表明抑肽酶可保护肾脏免受缺血再灌注损伤。它们还表明抑肽酶可能通过影响凋亡信号传导和炎性细胞因子产生来实现这一点。在可以预期发生肾脏缺血再灌注损伤的临床情况下,只要能够进行充分的肝素化,抑肽酶是一种潜在的治疗措施。

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