Stein H J, Esplugues J, Whittle B J, Bauerfeind P, Hinder R A, Blum A L
Department of Gastroenterology, CHUV, Lausanne, Switzerland.
Surgery. 1989 Aug;106(2):318-23: discussion 323-4.
Oxygen radical release has been proposed as a pathogenetic factor in the formation of acute gastric mucosal injury. We assessed the ability of the naturally occurring oxygen radical generating system hypoxanthine/xanthine oxidase (HX/XO) to cause gross gastric mucosal injury and measured the effect on regional mucosal blood flow. Local intra-arterial infusion of HX/XO into the vascular network of the stomach caused marked gross mucosal injury in the antrum and corpus. This injury occurred even in the absence of exogenous luminal acid and was aggravated by luminal acidification with 1 ml of 0.1N HCl. The selective oxygen radical scavenger superoxide dismutase (SOD) prevented mucosal injury caused by HX/XO. The effects of HX/XO and SOD were not mediated by alterations in regional gastric mucosal blood flow, as measured by the radiolabeled microspheres and reference sample method. These findings suggest that oxygen radicals are capable of causing substantial gastric mucosal injury by a direct cytotoxic effect independent of luminal acid or mucosal blood supply and give support to the concept that oxygen radical release may be a major primary pathogenetic factor in the development of acute gastric mucosal injury.
氧自由基释放被认为是急性胃黏膜损伤形成的一个致病因素。我们评估了天然存在的氧自由基生成系统次黄嘌呤/黄嘌呤氧化酶(HX/XO)导致明显胃黏膜损伤的能力,并测定了其对局部黏膜血流的影响。将HX/XO局部动脉内注入胃的血管网络会导致胃窦和胃体出现明显的肉眼可见的黏膜损伤。即使在没有外源性腔内酸的情况下这种损伤也会发生,并且用1毫升0.1N盐酸使腔内酸化会加重这种损伤。选择性氧自由基清除剂超氧化物歧化酶(SOD)可预防HX/XO引起的黏膜损伤。通过放射性微球和参考样品法测量发现,HX/XO和SOD的作用不是由局部胃黏膜血流的改变介导的。这些发现表明,氧自由基能够通过独立于腔内酸或黏膜血液供应的直接细胞毒性作用引起严重的胃黏膜损伤,并支持氧自由基释放可能是急性胃黏膜损伤发生的主要原发性致病因素这一概念。