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阿糖鸟苷的抗贾第虫活性。机制研究。

Antigiardial activity of guanine arabinoside. Mechanism studies.

作者信息

Miller R L, Nelson D J, LaFon S W, Miller W H, Krenitsky T A

出版信息

Biochem Pharmacol. 1987 Aug 1;36(15):2519-25. doi: 10.1016/0006-2952(87)90525-9.

Abstract

Guanine arabinoside (araG) inhibited the in vitro growth of Giardia lamblia WB with an ED50 value of 4 microM. The inhibition was prevented completely by 2'-deoxyguanosine, prevented partially by guanine and guanosine, and not prevented by adenine, adenosine or 2'-deoxyadenosine. Extracts of G. lamblia grown in the presence of [8-3H]araG contained radiolabeled araGMP, araGDP and araGTP. The formation of araGTP during the exponential phase of cell growth increased with time and was dependent upon the araG concentration. AraG was incorporated into G. lamblia DNA in a time-dependent manner at a ratio of 1 araG for each 27 2'-deoxyguanosine residues. Short-term exposure of growing cultures to araG was inhibitory to DNA synthesis but not to RNA or protein synthesis. Over an extended period, synthesis of all three macromolecules was depressed. Attempts to measure araG phosphorylation by cell-free extracts of G. lamblia under a variety of nucleoside kinase and nucleoside phosphotransferase assay conditions were unsuccessful. In an attempt to understand further the action of araG, the metabolic pathways of guanine, guanosine and 2'-deoxyguanosine were delineated in detail. The presence of araG did not appear to cause any major alterations in the metabolism of these compounds; however, it was accompanied by a 3- to 4-fold increase in the endogenous pools of ATP and GTP.

摘要

阿糖鸟苷(araG)可抑制蓝氏贾第鞭毛虫WB株的体外生长,其半数有效浓度(ED50)为4微摩尔。2'-脱氧鸟苷可完全阻止这种抑制作用,鸟嘌呤和鸟苷可部分阻止,而腺嘌呤、腺苷或2'-脱氧腺苷则不能阻止。在[8-3H]araG存在下生长的蓝氏贾第鞭毛虫提取物中含有放射性标记的araGMP、araGDP和araGTP。细胞生长指数期araGTP的形成随时间增加,且依赖于araG的浓度。阿糖鸟苷以时间依赖性方式掺入蓝氏贾第鞭毛虫DNA中,其比例为每27个2'-脱氧鸟苷残基对应1个阿糖鸟苷。将生长中的培养物短期暴露于阿糖鸟苷可抑制DNA合成,但不抑制RNA或蛋白质合成。在较长时间内,所有三种大分子的合成均受到抑制。在多种核苷激酶和核苷磷酸转移酶测定条件下,尝试用蓝氏贾第鞭毛虫的无细胞提取物测量阿糖鸟苷磷酸化均未成功。为了进一步了解阿糖鸟苷的作用,详细描绘了鸟嘌呤、鸟苷和2'-脱氧鸟苷的代谢途径。阿糖鸟苷的存在似乎并未引起这些化合物代谢的任何重大改变;然而,它伴随着ATP和GTP内源性池增加3至4倍。

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