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环孢素A对大鼠黏膜肥大细胞及相关蛋白酶RMCPII的影响。

Effect of cyclosporin A on rat mucosal mast cells and the associated protease RMCPII.

作者信息

Cummins A G, Munro G H, Ferguson A

机构信息

Gastro-Intestinal Unit, University of Edinburgh, Scotland, UK.

出版信息

Clin Exp Immunol. 1988 Apr;72(1):136-40.

Abstract

The effects of Cyclosporin A (CyA) on rat mucosal mast cells (MMC) have been investigated by cell counts in the jejunal mucosa and assays of the MMC-specific granule protease RMCPII in tissues and serum. CyA was administered by subcutaneous injection; for the majority of experiments the rats received 50 mg/kg daily for 3 days as a loading dose, then 50 mg/kg on alternate days. Treatment with this drug has two actions on MMC, a gradual reduction in the number of MMC and in the tissue content of RMCPII in the jejunum; and a rapid fall in the serum concentration of RMCPII, detectable 3 h after i.v. administration of CyA, 50 mg/kg. These phenomena were demonstrated in normal rats and in animals with an expanded jejunal MMC population due to graft vs host reaction or recent helminth infection. The functional relevance of the MMC depletion was demonstrated in immune rats given CyA for 3 days prior to induction of systemic anaphylaxis; intestinal permeability to i.v. Evan's blue was significantly reduced by CyA treatment. We suggest that CyA depletes intestinal MMC by suppression of T-cell-mediated regulatory stimuli to proliferation of mast cell precursors and/or their migration. The effects of the drug on serum RMCPII, evident before there were changes in the number of intestinal MMC, indicate that it also suppresses the secretion of granule mediators by MMC, probably indirectly via effects on mucosal T cells.

摘要

通过对空肠黏膜进行细胞计数以及对组织和血清中黏膜肥大细胞(MMC)特异性颗粒蛋白酶RMCPII进行检测,研究了环孢素A(CyA)对大鼠MMC的影响。CyA通过皮下注射给药;在大多数实验中,大鼠作为负荷剂量每天接受50mg/kg,持续3天,然后隔天接受50mg/kg。用这种药物治疗对MMC有两种作用,一是MMC数量和空肠中RMCPII的组织含量逐渐减少;二是静脉注射50mg/kg CyA后3小时可检测到血清中RMCPII浓度迅速下降。这些现象在正常大鼠以及由于移植物抗宿主反应或近期蠕虫感染而导致空肠MMC数量增加的动物中均得到证实。在诱导全身性过敏反应前3天给予CyA的免疫大鼠中,证实了MMC耗竭的功能相关性;CyA治疗可显著降低静脉注射伊文思蓝后的肠道通透性。我们认为,CyA通过抑制T细胞介导的对肥大细胞前体增殖和/或其迁移的调节刺激来消耗肠道MMC。该药物对血清RMCPII的影响在肠道MMC数量发生变化之前就很明显,这表明它还可能通过对黏膜T细胞的作用间接抑制MMC颗粒介质的分泌。

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