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环孢素治疗的急性血清病兔出现严重的全身血管坏死。

Severe systemic vascular necrosis in cyclosporin-treated rabbits with acute serum sickness.

作者信息

Neild G H, Ivory K, Williams D G

出版信息

Br J Exp Pathol. 1984 Dec;65(6):731-43.

Abstract

Rabbits given acute serum sickness (ASS) and treated with cyclosporin A (CyA) developed a severe, systemic vascular injury, which was not similar to that normally seen in ASS. Thirty-three NZW rabbits received a single intravenous injection of 250 mg/kg bovine serum albumen (BSA) with or without endotoxin (5 micrograms/kg), on day 0. Groups of rabbits were given intramuscular CyA as follows: 15 mg/kg/day from day -2 to +8, or 25 mg/kg/day from day -2 to +3 or day 0 to 5. Muscular arteries of the heart and splanchnic organs developed an arterial injury in which there was extensive fibrinoid necrosis of the vessel wall but little or none of the mononuclear cell reaction that is normally associated with the arteritis of ASS. A microvascular injury also occurred which led to interstitial haemorrhage in the gastric mucosa and multi-focal necrosis in the heart and liver. These lesions were seen with equal frequency in all groups of rabbits with serum sickness who received CyA, irrespective of whether they also received endotoxin. We suggest that CyA altered the host inflammatory response to the injury initiated by the BSA-anti-BSA immune complexes and this led to enhanced vascular injury. The inhibition by CyA of the perivascular cellular reaction suggests that this reaction may be mediated by T lymphocytes. This model should provide further insight into the pathogenesis of arteritis, as well as the mechanisms of cyclosporin toxicity.

摘要

给予急性血清病(ASS)并接受环孢素A(CyA)治疗的兔子出现了严重的全身性血管损伤,这种损伤与ASS中通常所见的不同。33只新西兰白兔在第0天接受单次静脉注射250mg/kg牛血清白蛋白(BSA),部分同时注射内毒素(5μg/kg)。兔子分组后接受肌肉注射CyA,方案如下:从第-2天至+8天为15mg/kg/天,或从第-2天至+3天或第0天至5天为25mg/kg/天。心脏和内脏器官的肌性动脉出现动脉损伤,表现为血管壁广泛的纤维蛋白样坏死,但单核细胞反应很少或没有,而单核细胞反应通常与ASS的动脉炎相关。还发生了微血管损伤,导致胃黏膜间质出血以及心脏和肝脏的多灶性坏死。在所有接受CyA的血清病兔子组中,无论是否同时接受内毒素,这些病变出现的频率相同。我们认为,CyA改变了宿主对BSA-抗BSA免疫复合物引发的损伤的炎症反应,从而导致血管损伤加重。CyA对血管周围细胞反应的抑制表明,这种反应可能由T淋巴细胞介导。该模型应能进一步深入了解动脉炎的发病机制以及环孢素毒性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a0d/2040997/1e8134bf5772/brjexppathol00096-0092-a.jpg

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