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大鼠局部动脉内给予活性氧代谢产物后的胃损伤。

Gastric damage following local intra-arterial administration of reactive oxygen metabolites in the rat.

作者信息

Esplugues J V, Whittle B J

机构信息

Department of Pharmacology, Wellcome Research Laboratories, Beckenham, Kent.

出版信息

Br J Pharmacol. 1989 Aug;97(4):1085-92. doi: 10.1111/j.1476-5381.1989.tb12565.x.

Abstract
  1. The effects of reactive oxygen metabolites on the rat gastric mucosa following close-arterial infusion into the left gastric artery have been determined by macroscopic and histological assessment. 2. Local intra-arterial infusion of hydrogen peroxide (0.6-1.3 mumol kg-1 min-1) induced mucosal injury, characterised by areas of pronounced disruption and haemorrhage, which was prevented by concurrent intravenous administration of catalase. 3. Local infusion of the superoxide generating system xanthine-oxidase and hypoxanthine likewise induced extensive haemorrhagic damage and necrosis of the mucosa. Prolonged incubation of this mixture (10 min) before administration, significantly reduced the degree of injury, indicating the lability of the products so formed. 4. The gastric mucosal injury induced by the superoxide generating system was inhibited by concurrent local infusion of superoxide dismutase (96 u kg-1 min-1), as was the associated increase in mucosal permeability to radiolabelled albumin. 5. Administration of catalase did not inhibit the gastric mucosal damage induced by infusion of xanthine oxidase-hypoxanthine, yet augmented the protective effects of a low dose of superoxide dismutase (46 u kg-1 min-1 i.a.). 6. These findings directly confirm that reactive oxygen metabolites can induce extensive gastric mucosal injury, supporting their role in the pathogenesis of gastric damage following ischaemia and hypotensive shock.
摘要
  1. 通过宏观和组织学评估,已确定了活性氧代谢产物经左胃动脉进行动脉内灌注后对大鼠胃黏膜的影响。2. 局部动脉内灌注过氧化氢(0.6 - 1.3 μmol·kg⁻¹·min⁻¹)可诱发黏膜损伤,其特征为明显的组织破坏和出血区域,同时静脉注射过氧化氢酶可预防这种损伤。3. 局部灌注超氧化物生成系统黄嘌呤氧化酶和次黄嘌呤同样会诱发广泛的出血性损伤和黏膜坏死。在给药前将该混合物长时间孵育(10分钟),可显著降低损伤程度,表明如此形成的产物不稳定。4. 同时局部灌注超氧化物歧化酶(96 u·kg⁻¹·min⁻¹)可抑制超氧化物生成系统诱发的胃黏膜损伤,以及与之相关的黏膜对放射性标记白蛋白通透性的增加。5. 过氧化氢酶的给药并未抑制黄嘌呤氧化酶 - 次黄嘌呤灌注诱发的胃黏膜损伤,但增强了低剂量超氧化物歧化酶(46 u·kg⁻¹·min⁻¹,动脉内给药)的保护作用。6. 这些发现直接证实活性氧代谢产物可诱发广泛的胃黏膜损伤,支持它们在缺血和低血压性休克后胃损伤发病机制中的作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33f7/1854633/e2adaa0a03fa/brjpharm00270-0100-a.jpg

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