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[邻氨基偶氮甲苯及其非致癌类似物对小鼠免疫抑制作用的机制]

[Mechanisms of the immunodepression caused by ortho-aminoazotoluene and its noncarcinogenic analog in mice].

作者信息

Kaledin V I, Glazko T T, Krass P M, Chesnokova V M

出版信息

Vopr Onkol. 1978;24(9):46-52.

PMID:706294
Abstract

Single injections of ortho-aminoazotoluene (OAT) or aminoazobenzene (AB) decrease the immune response of DD mice to the strain-nonspecific Krebs-2 tumor. The immunosuppressive action of AB is due to its toxicity for lymphoid cells, whereas the OAT effect is mediated by adrenal glands. After OAT injection,II-oxycorticosteroids level is elevated although their production by adrenal glands is not increased. The accumulation of glucocorticoids in blood after OAT injection is assumed to be the result of a decreased hormone utilization because of the blockade of receptor proteins or metabolizing enzymes in liver cells by a carcinogen.

摘要

单次注射邻氨基偶氮甲苯(OAT)或氨基偶氮苯(AB)可降低DD小鼠对非菌株特异性克雷布斯-2肿瘤的免疫反应。AB的免疫抑制作用归因于其对淋巴细胞的毒性,而OAT的作用是由肾上腺介导的。注射OAT后,II-氧皮质类固醇水平升高,尽管肾上腺对其产生并未增加。OAT注射后血液中糖皮质激素的积累被认为是由于致癌物阻断肝细胞中的受体蛋白或代谢酶导致激素利用减少的结果。

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