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硫嘌呤S-甲基转移酶和吲哚乙胺N-甲基转移酶介导亚碲酸盐形成甲基化碲化合物。

Thiopurine S‑methyltransferase- and indolethylamine N‑methyltransferase-mediated formation of methylated tellurium compounds from tellurite.

作者信息

Tanaka Yu-Ki, Takata Ayuka, Takahashi Karin, Yamagishi Yoshikazu, Fukumoto Yasunori, Suzuki Noriyuki, Ogra Yasumitsu

机构信息

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo, Chiba, 260-8675, Japan.

Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo, Chiba, 260-8670, Japan.

出版信息

Arch Toxicol. 2025 Jan;99(1):237-244. doi: 10.1007/s00204-024-03890-4. Epub 2024 Oct 17.

Abstract

Tellurium (Te) is a metalloid widely used in various industries. However, its toxicological impact on humans is poorly understood. In this study, we investigated the role of two methyltransferases, thiopurine S‑methyltransferase (TPMT) and indolethylamine N‑methyltransferase (INMT), in the methylation of tellurite, an inorganic Te oxyanion. The products of the reaction of Te compounds catalyzed by recombinant human TPMT and/or INMT were analyzed by liquid chromatography hyphenated to inductively coupled plasma mass spectrometry (LC-ICP-MS) and gas chromatography mass spectrometry (GC-MS). We found that TPMT catalyzes the methylation of non-methylated Te and methanetellurol to generate dimethyltelluride. On the other hand, INMT catalyzes the methylation of methanetellurol and dimethyltelluride to produce trimethyltelluronium ion, a metabolite excreted into animal urine. We conclude that TPMT and INMT are cooperatively responsible for the detoxification of Te oxyanions through methylation to form trimethyltelluronium ions.

摘要

碲(Te)是一种广泛应用于各种行业的类金属。然而,人们对其对人类的毒理学影响了解甚少。在本研究中,我们研究了两种甲基转移酶,硫嘌呤S-甲基转移酶(TPMT)和吲哚乙胺N-甲基转移酶(INMT),在亚碲酸盐(一种无机碲氧阴离子)甲基化中的作用。通过液相色谱与电感耦合等离子体质谱联用(LC-ICP-MS)和气相色谱-质谱联用(GC-MS)分析重组人TPMT和/或INMT催化的碲化合物反应产物。我们发现TPMT催化未甲基化的碲和甲碲醇甲基化生成二甲基碲。另一方面,INMT催化甲碲醇和二甲基碲甲基化生成三甲基碲鎓离子,这是一种排泄到动物尿液中的代谢物。我们得出结论,TPMT和INMT通过甲基化形成三甲基碲鎓离子协同负责碲氧阴离子的解毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ef/11742336/6d6050fa363f/204_2024_3890_Fig1_HTML.jpg

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