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乙胺嘧啶体外诱导人淋巴细胞的改变。作用机制及效应的逆转

Pyrimethamine-induced alterations in human lymphocytes in vitro. Mechanisms and reversal of the effect.

作者信息

Bygbjerg I C

出版信息

Acta Pathol Microbiol Immunol Scand C. 1985 Aug;93(4):183-8. doi: 10.1111/j.1699-0463.1985.tb02942.x.

Abstract

It has previously been shown that the antiprotozoal drug pyrimethamine (PYR) in concentrations corresponding to those obtained in clinical practice temporarily suppressed the proliferation of phytohaemagglutinin (PHA-) stimulated human lymphocytes in vitro; 10-fold higher concentrations permanently suppressed PHA-stimulated cells, as indicated by decreased numbers of cells and DNA synthesis. In the present study, it was found that the 3H-deoxyuridine incorporation in PHA-stimulated lymphocytes was suppressed by PYR, and that PYR caused defective deoxyuridine suppression of 14C-thymidine incorporation. The effects of PYR were completely corrected by low concentrations of folinic acid and high concentrations of folic acid, indicating that the basic mechanism of action of PYR is competitive blocking of dihydrofolate reductase. However, the effect of PYR was poorly corrected by exogenous thymidine; therefore, reduced thymidylate synthesis cannot be the sole consequence of PYR exposure. It is suggested that an additional folate-dependent factor plays an important role in the antimitotic activity of PYR on lymphocytes.

摘要

先前已经表明,抗寄生虫药物乙胺嘧啶(PYR)在临床实践中所达到的浓度下,可在体外暂时抑制植物血凝素(PHA)刺激的人淋巴细胞的增殖;浓度高出10倍时则会永久性抑制PHA刺激的细胞,表现为细胞数量减少和DNA合成降低。在本研究中,发现PYR可抑制PHA刺激的淋巴细胞中3H-脱氧尿苷的掺入,并且PYR会导致14C-胸苷掺入的脱氧尿苷抑制出现缺陷。低浓度的亚叶酸和高浓度的叶酸可完全纠正PYR的作用,表明PYR的基本作用机制是对二氢叶酸还原酶的竞争性阻断。然而,外源性胸苷对PYR的作用纠正效果不佳;因此,胸苷酸合成减少并非PYR作用的唯一结果。提示另一个叶酸依赖性因子在PYR对淋巴细胞的抗有丝分裂活性中起重要作用。

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