Nilsson U A, Lundgren O, Haglind E, Bylund-Fellenius A C
Department of Biochemistry and Biophysics, Chalmers University of Technology, Gothenburg, Sweden.
Am J Physiol. 1989 Sep;257(3 Pt 1):G409-14. doi: 10.1152/ajpgi.1989.257.3.G409.
Free radical formation was studied with electron spin resonance during 2 h of intestinal ischemia in the cat, at a blood flow less than 5 ml.min-1.100 g-1, followed by 30-min reperfusion. A modification of the spin trapping technique was used to stabilize highly reactive free radicals. The rate of secondary radical formation was 0.32 +/- 0.06 mumol.min-1.100 g intestine-1 before ischemia and increased to a maximum of 0.66 +/- 0.09 mumol.min-1.100 g-1 during the first minutes of reperfusion (mean +/- SE, n = 5). This could be prevented either by maintaining intestinal blood flow at 8-15 ml.min-1.100 g-1, by administering allopurinol before and during ischemia, or by perfusing the intestinal lumen with an O2-saturated buffer solution during ischemia, resulting in maximum rates of radical production during reperfusion of 0.37 +/- 0.04 (n = 6), 0.33 +/- 0.04 (n = 5), and 0.39 +/- 0.13 mumol.min-1.100 g-1 (n = 5), respectively. The results demonstrate that free radicals are produced in the intestine during reperfusion after a period of reduced blood flow below a certain critical level, and that inhibition of xanthine oxidase and prevention of hypoxia will eliminate this radical production.
在猫肠道缺血2小时期间,当血流量低于5毫升·分钟⁻¹·100克⁻¹时,采用电子自旋共振研究自由基的形成,随后进行30分钟的再灌注。采用自旋捕获技术的一种改进方法来稳定高反应性自由基。缺血前二级自由基形成速率为0.32±0.06微摩尔·分钟⁻¹·100克肠道⁻¹,在再灌注的最初几分钟内增加至最大值0.66±0.09微摩尔·分钟⁻¹·100克⁻¹(平均值±标准误,n = 5)。这可以通过将肠道血流量维持在8 - 15毫升·分钟⁻¹·100克⁻¹、在缺血前和缺血期间给予别嘌呤醇或在缺血期间用氧气饱和缓冲溶液灌注肠腔来预防,导致再灌注期间自由基产生的最大速率分别为0.37±0.04(n = 6)、0.33±0.04(n = 5)和0.39±0.13微摩尔·分钟⁻¹·100克⁻¹(n = 5)。结果表明,在一段时间的低于一定临界水平的血流减少后再灌注期间,肠道会产生自由基,并且抑制黄嘌呤氧化酶和预防缺氧将消除这种自由基产生。