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抗抑郁药引起的大鼠腹膜肥大细胞组胺和5-羟色胺分泌的变化

Changes in histamine and serotonin secretion from rat peritoneal mast cells caused by antidepressants.

作者信息

Ferjan I, Erjavec F

机构信息

Department of Pharmacology, Medical Faculty, University of Ljubljana, Slovenia.

出版信息

Inflamm Res. 1996 Mar;45(3):141-4. doi: 10.1007/BF02265168.

Abstract

Psychotropic agents modify the release of histamine and serotonin from rat peritoneal mast cells induced by compound 48/80. Some antidepressants, such as clomipramine and fluoxetine (10(-8) - 10(-5) mol/l), increase the percentage of released serotonin in the incubation medium but have no effect on histamine release. In contrast, amitriptyline (10(-4) mol/l) inhibits the secretion of histamine and permits that of serotonin. The varying effects of antidepressants on the secretion of histamine and serotonin could be explained either by a differential mechanism of secretion of both amines from mast cells or by a selective effect of drugs on the reuptake of serotonin into mast cells after stimulation by compound 48/80. These hypotheses were further investigated in our present study on rat peritoneal mast cells. Our findings suggest that antidepressants influence the secretion and the reuptake process of amines used. Their effects depend on the concentration of the drug. At lower concentrations, antidepressants (amitriptyline, doxepine and clomipramine) produce no effect on the secretion of the amines whereas at higher concentrations ( > 10(-5) mol/l), they inhibit the release. Additionally, mast cells are capable of removing released serotonin from the incubation medium. Serotonin uptake is an active process which increases with the time of incubation with exogenous serotonin and depends on the presence of extracellular Ca2+ and on the temperature of the medium. Preincubation of mast cells with antidepressants inhibits the reuptake of serotonin into mast cells and thus increases the concentration of serotonin in the incubation medium. Since the reuptake of serotonin is a relatively slow process, the elevation of serotonin in the medium is evident only after longer times of incubation.

摘要

精神药物可改变由化合物48/80诱导的大鼠腹膜肥大细胞中组胺和5-羟色胺的释放。一些抗抑郁药,如氯米帕明和氟西汀(10⁻⁸ - 10⁻⁵mol/L),可增加孵育培养基中5-羟色胺的释放百分比,但对组胺释放无影响。相反,阿米替林(10⁻⁴mol/L)抑制组胺分泌而允许5-羟色胺分泌。抗抑郁药对组胺和5-羟色胺分泌的不同作用,既可以用肥大细胞中这两种胺类分泌的不同机制来解释,也可以用药物对化合物48/80刺激后5-羟色胺重新摄取到肥大细胞中的选择性作用来解释。在我们目前对大鼠腹膜肥大细胞的研究中,对这些假设进行了进一步研究。我们的研究结果表明,抗抑郁药会影响所用胺类的分泌和重新摄取过程。它们的作用取决于药物浓度。在较低浓度下,抗抑郁药(阿米替林、多塞平和氯米帕明)对胺类分泌无影响,而在较高浓度(>10⁻⁵mol/L)时,它们会抑制释放。此外,肥大细胞能够从孵育培养基中清除释放的5-羟色胺。5-羟色胺摄取是一个活跃过程,随着与外源性5-羟色胺孵育时间的延长而增加,并取决于细胞外Ca²⁺的存在和培养基的温度。用抗抑郁药预孵育肥大细胞会抑制5-羟色胺重新摄取到肥大细胞中,从而增加孵育培养基中5-羟色胺的浓度。由于5-羟色胺的重新摄取是一个相对缓慢的过程,培养基中5-羟色胺的升高仅在孵育较长时间后才明显。

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