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[氢化可的松对人白细胞趋化性迁移的抑制作用]

[The inhibitory effect of hydrocortisone on the chemotactic migration of human leukocytes].

作者信息

Liu Z M, Xu R B

机构信息

Department of Pathophysiology, Second Military Medical College, Shanghai.

出版信息

Sheng Li Xue Bao. 1990 Apr;42(2):163-8.

PMID:2374935
Abstract

Random migration (RM) and chemotactic migration (ChtM) of human leukocytes to yeast activated serum were studied with the modified Boyden chamber method. Both RM and ChtM showed circadian rhythm. Leukocytes migrated most rapidly at night. The difference between the peak (0:00) and trough values (8:00) of RM and ChtM was significant statistically (P less than 0.01). ChtM was inhibited by hydrocortisone (F) of physiological concentration (10(-9)-10(-7) mol/L) which was dose-dependent and completely antagonized by the competitive antagonist, RU38486. The inhibitory effect was much more evident with higher dose (more than 10(-5) mol/L) and it was also reversed by RU38486, but only partially. It is suggested that glucocorticoids (GC) may be a physiological regulator of the activity of leukocytes and its inhibitory action on ChtM may be involved in antiinflammatory mechanisms of GC of pharmacological doses. The action of physiological and pharmacological concentration of GC may be mediated by low affinity specific binding sites of glucocorticoid receptors.

摘要

采用改良的博伊登小室法研究了人白细胞向酵母激活血清的随机迁移(RM)和趋化迁移(ChtM)。RM和ChtM均呈现昼夜节律。白细胞在夜间迁移最为迅速。RM和ChtM的峰值(0:00)与谷值(8:00)之间的差异具有统计学意义(P小于0.01)。生理浓度(10⁻⁹ - 10⁻⁷ mol/L)的氢化可的松(F)对ChtM有抑制作用,且呈剂量依赖性,并被竞争性拮抗剂RU38486完全拮抗。高剂量(超过10⁻⁵ mol/L)时抑制作用更为明显,且同样可被RU38486逆转,但只是部分逆转。提示糖皮质激素(GC)可能是白细胞活性的生理调节因子,其对ChtM的抑制作用可能参与了药理剂量GC的抗炎机制。生理和药理浓度的GC作用可能由糖皮质激素受体的低亲和力特异性结合位点介导。

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