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基质金属蛋白酶抑制可保护失血性休克中的肝脏完整性。

Matrix metalloproteinase inhibition protects hepatic integrity in hemorrhagic shock.

作者信息

Santibanez-Gallerani A S, Barber A E, Williams S J, Davis S, Zhao Y, Shires G T

机构信息

Department of Surgery, University of Nevada School of Medicine, Las Vegas, NV 89102, USA.

出版信息

J Gastrointest Surg. 2000 Sep-Oct;4(5):536-41. doi: 10.1016/s1091-255x(00)80098-0.

Abstract

Hemorrhagic shock increases cytokines, such as tumor necrosis factor-alpha (TNF-alpha), and interleukin-6 (IL-6), and compromises hepatic function and integrity. The production of TNF-alpha involves a cascade reaction regulated by the enzyme TNF-alpha convertase. The purpose of this study was to examine the effects of matrix metalloproteinase inhibitor (MMPI) (British Biotech 1101) in vivo on hepatic integrity in a rat model of hemorrhagic shock. Sprague-Dawley rats (n = 26) were divided as follows: hemorrhagic shock (group 1) and hemorrhagic shock plus MMPI (group 2). TNF-alpha, IL-6, and hepatic membrane potentials (Em) were obtained. The administration of MMPI significantly decreased TNF-alpha levels (P <0.001) and stabilized the membrane potential at -30 mV as compared to the depolarized membrane potential at -20 mV for hemorrhagic shock without MMPI. IL-6 levels were not affected by the MMPI. This study demonstrates that MMPI decreases TNF-alpha levels and protects hepatic integrity in hemorrhagic shock, as evidenced by the stabilization of the membrane potential, independent of the mean arterial pressure. The hepatic protection is closely related to the decrease in TNF-alpha levels seen in the portal circulation.

摘要

失血性休克会增加细胞因子,如肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6),并损害肝功能和肝脏完整性。TNF-α的产生涉及由TNF-α转换酶调节的级联反应。本研究的目的是在失血性休克大鼠模型中检测基质金属蛋白酶抑制剂(MMPI)(英国生物技术公司1101)对肝脏完整性的体内影响。将26只Sprague-Dawley大鼠分为以下几组:失血性休克组(第1组)和失血性休克加MMPI组(第2组)。检测TNF-α、IL-6和肝细胞膜电位(Em)。与未使用MMPI的失血性休克时-20mV的去极化膜电位相比,给予MMPI可显著降低TNF-α水平(P<0.001)并使膜电位稳定在-30mV。IL-6水平不受MMPI影响。本研究表明,MMPI可降低TNF-α水平并保护失血性休克时的肝脏完整性,膜电位的稳定证明了这一点,且与平均动脉压无关。肝脏保护与门静脉循环中TNF-α水平的降低密切相关。

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