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内源性一氧化氮在维持大鼠微血管完整性以抵抗腹部剖腹术后广泛的血浆渗漏中的作用。

Endogenous nitric oxide in the maintenance of rat microvascular integrity against widespread plasma leakage following abdominal laparotomy.

作者信息

László F, Whittle B J

机构信息

Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest.

出版信息

Br J Pharmacol. 1999 Jan;126(2):515-21. doi: 10.1038/sj.bjp.0702322.

Abstract
  1. The role of nitric oxide (NO) in the maintenance of microvascular integrity during minor surgical manipulation has been evaluated in the rat. 2. The NO synthase inhibitors, NG-nitro-L-arginine methyl ester (L-NAME, 5 mg kg(-1), s.c.) and N(G)-monomethyl-L-arginine (L-NMMA, 50 mg kg(-1), s.c.) had no effect on microvascular leakage of radiolabelled albumin over 1 h in the stomach, duodenum, jejunum, colon, lung and kidney in the un-operated conscious or pentobarbitone-anaesthetized rat. 3. In contrast, in anaesthetized rats with a midline abdominal laparotomy (5 cm), L-NAME (1-5 mg kg(-1), s.c.) or L-NMMA (12.5-50 mg kg(-1), s.c.) dose-dependently increased gastrointestinal, renal and pulmonary vascular leakage, effects reversed by L-arginine pretreatment (300 mg kg(-1), s.c., 15 min). These actions were not observed in anaesthetized rats that had only received a midline abdominal skin incision (5 cm). 4. Pretreatment with a rabbit anti-rat neutrophil serum (0.4 ml kg(-1), i.p.), 4 h before laparotomy, abolished the plasma leakage induced by L-NAME in all the organs investigated. 5. These results indicate that the following abdominal laparotomy, inhibition of constitutive NO synthase provokes vascular leakage in the general microcirculation, by a process that may involve neutrophils. Such effects could thus confound studies on the microvascular actions of NO synthase inhibitors using acute surgically prepared in vivo models. The findings thus suggest that constitutively-formed NO has a crucial role in the maintenance of acute microvascular integrity following abdominal surgical intervention.
摘要
  1. 一氧化氮(NO)在大鼠小手术操作过程中对维持微血管完整性的作用已得到评估。2. NO合酶抑制剂Nω-硝基-L-精氨酸甲酯(L-NAME,5 mg·kg⁻¹,皮下注射)和N(G)-单甲基-L-精氨酸(L-NMMA,50 mg·kg⁻¹,皮下注射)对未手术的清醒或戊巴比妥麻醉大鼠的胃(距幽门1 cm)、十二指肠、空肠、结肠、肺和肾中放射性标记白蛋白在1小时内的微血管渗漏没有影响。3. 相比之下,在进行了腹部正中剖腹术(5 cm)的麻醉大鼠中,L-NAME(1 - 5 mg·kg⁻¹,皮下注射)或L-NMMA(12.5 - 50 mg·kg⁻¹,皮下注射)剂量依赖性地增加了胃肠道、肾脏和肺部的血管渗漏,L-精氨酸预处理(300 mg·kg⁻¹,皮下注射,15分钟)可逆转这些作用。在仅接受腹部正中皮肤切口(5 cm)的麻醉大鼠中未观察到这些作用。4. 在剖腹术前4小时用兔抗大鼠中性粒细胞血清(0.4 ml·kg⁻¹,腹腔注射)预处理,可消除L-NAME在所有研究器官中诱导的血浆渗漏。5. 这些结果表明,在腹部剖腹术后,抑制组成型NO合酶会通过一个可能涉及中性粒细胞的过程引发全身微循环中的血管渗漏。因此,这些效应可能会混淆使用急性手术制备的体内模型对NO合酶抑制剂微血管作用的研究。这些发现表明,组成型生成的NO在腹部手术干预后维持急性微血管完整性方面具有关键作用。

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