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体外酯化抗炎皮质类固醇在淋巴细胞中的掺入增加。

Increase in incorporation into lymphocytes in vitro of esterified anti-inflammatory corticosteroids.

作者信息

Mizushima Y, Igarashi R, Hoshi K, Muramatsu M, Fujita A

出版信息

Agents Actions. 1986 Oct;19(1-2):123-6. doi: 10.1007/BF01977267.

Abstract

Corticosteroids esterified at C-17 and C-21 such as hydrocortisone 17-butyrate 21-propionate (HBP) and prednisolone 17-valerate 21-acetate (PVA) inhibited PHA-induced blastogenesis of human blood lymphocytes more intensively than hydrocortisone (HC) and prednisolone (PSL), the parent corticosteroids. When lymphocytes were incubated with HBP or HC, the total amount of HBP incorporated into lymphocytes was much larger than that of HC. The amount of HBP bound specifically to the receptors was also increased, which may be due to the increased concentration of corticosteroid in lymphocytes. These results suggest that the increased incorporation of the esterified corticosteroids into cells would be most important to produce an intensive biological activity.

摘要

在C-17和C-21位酯化的皮质类固醇,如氢化可的松17-丁酸酯21-丙酸酯(HBP)和泼尼松龙17-戊酸酯21-乙酸酯(PVA),比母体皮质类固醇氢化可的松(HC)和泼尼松龙(PSL)更强烈地抑制PHA诱导的人血淋巴细胞增殖。当淋巴细胞与HBP或HC孵育时,掺入淋巴细胞的HBP总量远大于HC。与受体特异性结合的HBP量也增加,这可能是由于淋巴细胞中皮质类固醇浓度增加所致。这些结果表明,酯化皮质类固醇进入细胞的增加对于产生强烈的生物活性最为重要。

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