ToxStrategies, Inc., Katy, TX 77494, USA.
Toxicol Lett. 2010 Mar 1;193(1):1-3. doi: 10.1016/j.toxlet.2009.11.023. Epub 2009 Dec 4.
Formaldehyde dehydrogenase, formally Class III alcohol dehydrogenase (ADH3), has recently been discovered to partially regulate nitrosothiol homeostasis by catalyzing the reduction of the endogenous nitrosylating agent S-nitrosoglutathione (GSNO). Several studies have implicated this enzyme, and in particular GSNO reduction, as playing an important role in conditions such as asthma, cardiovascular disease, and immune function. While ADH3 has received considerable attention in the biomedical literature where it is often referred to as GSNO reductase (GSNOR), ADH3-mediated GSNO reduction has received comparatively less attention in the environmental toxicology community. Herein, evidences for a role of ADH3 in cell signaling through thiol homeostasis is highlighted, underscoring that the enzyme functions more broadly than to metabolize formaldehyde.
甲醛脱氢酶,正式分类为 III 类醇脱氢酶(ADH3),最近被发现通过催化内源性硝化试剂 S-亚硝基谷胱甘肽(GSNO)的还原,部分调节亚硝基硫醇的动态平衡。有几项研究表明,这种酶,特别是 GSNO 的还原,在哮喘、心血管疾病和免疫功能等疾病中起着重要作用。虽然 ADH3 在生物医学文献中受到了相当多的关注,在那里它通常被称为 GSNO 还原酶(GSNOR),但 ADH3 介导的 GSNO 还原在环境毒理学领域受到的关注相对较少。本文强调了 ADH3 通过硫醇动态平衡在细胞信号传导中作用的证据,强调了该酶的功能不仅限于代谢甲醛。