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前列腺素I2对缺血诱导的肝细胞损伤的细胞保护作用。

Cytoprotective effect of prostaglandin I2 on ischemia-induced hepatic cell injury.

作者信息

Sikujara O, Monden M, Toyoshima K, Okamura J, Kosaki G

出版信息

Transplantation. 1983 Sep;36(3):238-43. doi: 10.1097/00007890-198309000-00002.

Abstract

The protective effect of prostaglandin I2 (PGI2) on ischemia-induced liver cell injury was investigated during 60-min, 75-min, and 90-min liver ischemia. Vehicle-treated rats tolerated the 75-min hepatic ischemia poorly. Only 25% of the rats in this group survived more than 7 days. However, the survival rate of PGI2-treated rats (350 ng/kg/min) significantly improved to 67%. Liver cell organelles were well-preserved by the PGI2 treatment. Adenosine triphosphate levels in the liver of the PGI2-treated rats were significantly higher than those of vehicle-treated rats at 60 min of reoxygenation following 75-min ischemia. Cyclic 3'-5' adenosine monophosphate levels markedly increased during 60-min PGI2 infusion. Cyclic 3'-5' guanosine monophosphate levels also significantly increased during the PGI2 infusion and were still higher than those of vehicle-treated rats at the end of the 75-min ischemia. Although the exact cytoprotective mechanism of PGI2 at the cellular level is still unclear, our results demonstrate that elevated ATP and cyclic nucleotides levels play an important role in liver cell preservation during ischemia.

摘要

在60分钟、75分钟和90分钟肝脏缺血期间,研究了前列腺素I2(PGI2)对缺血诱导的肝细胞损伤的保护作用。用赋形剂处理的大鼠对75分钟的肝脏缺血耐受性较差。该组中只有25%的大鼠存活超过7天。然而,PGI2处理的大鼠(350 ng/kg/分钟)的存活率显著提高到67%。PGI2处理可使肝细胞细胞器保存良好。在75分钟缺血后复氧60分钟时,PGI2处理大鼠肝脏中的三磷酸腺苷水平显著高于用赋形剂处理的大鼠。在60分钟PGI2输注期间,环磷腺苷水平显著升高。在PGI2输注期间,环磷鸟苷水平也显著升高,并且在75分钟缺血结束时仍高于用赋形剂处理的大鼠。虽然PGI2在细胞水平的确切细胞保护机制仍不清楚,但我们的结果表明,升高的三磷酸腺苷和环核苷酸水平在缺血期间的肝细胞保存中起重要作用。

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