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急性多灶性胃肠道梗死的血管超敏反应模型

A vascular hypersensitivity model of acute multifocal gastrointestinal infarction.

作者信息

Hudson M, Piasecki C, Wakefield A J, Sankey E A, Dhillon A P, Osborne M, Sim R, Pounder R E

机构信息

University Department of Medicine, Royal Free Hospital School of Medicine, London, UK.

出版信息

Dig Dis Sci. 1994 Mar;39(3):534-9. doi: 10.1007/BF02088338.

Abstract

We have investigated the hypothesis that submucosal vasculitis may account for the patchy transmural inflammation observed in Crohn's disease. Test ferrets (N = 11) were sensitized to human albumin. Five days after the last sensitization injection, human albumin microspheres (15-150 microns diameter) were injected intraarterially into the mesenteric circulation of a defined loop of mid-gut. Six control ferrets showed no histological abnormality at either 48 hr or two weeks after intraarterial injection. At 48 hr, five of six presensitized ferrets demonstrated submucosal vasculitis with fibrinoid necrosis. In two cases there was transmural inflammation and mucosal ulceration. A further five presensitized ferrets received weekly subcutaneous human albumin injections following the mesenteric intraarterial injection of albumin microspheres: after two weeks one animal demonstrated mild perivascular inflammatory changes and another demonstrated vasculitis. One of the two animals with transmural inflammation and mucosal ulceration at 48 hr, and the animal with vasculitis at two weeks, had precipitating antibodies to human serum albumin. This model demonstrates that an immune-mediated submucosal vasculitis can sometimes result in discontinuous transmural inflammation of the intestinal wall.

摘要

我们研究了以下假说

黏膜下血管炎可能是克罗恩病中观察到的斑片状透壁性炎症的原因。对11只实验雪貂用人类白蛋白进行致敏。在最后一次致敏注射后5天,将直径为15 - 150微米的人类白蛋白微球经动脉注射到中肠特定肠袢的肠系膜循环中。6只对照雪貂在动脉内注射后48小时或两周时均未显示组织学异常。在48小时时,6只预先致敏的雪貂中有5只表现出伴有纤维蛋白样坏死的黏膜下血管炎。2例出现透壁性炎症和黏膜溃疡。在肠系膜动脉内注射白蛋白微球后,另外5只预先致敏的雪貂每周接受皮下注射人类白蛋白:两周后,1只动物表现出轻度血管周围炎症变化,另1只表现出血管炎。在48小时时出现透壁性炎症和黏膜溃疡的2只动物中的1只,以及在两周时出现血管炎的动物,具有针对人类血清白蛋白的沉淀抗体。该模型表明,免疫介导的黏膜下血管炎有时可导致肠壁的间断性透壁性炎症。

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