首页    期刊浏览 2024年11月30日 星期六
登录注册

文章基本信息

  • 标题:GABAA receptor target of tetramethylenedisulfotetramine
  • 本地全文:下载
  • 作者:Chunqing Zhao ; Sung Hee Hwang ; Bruce A. Buchholz
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2014
  • 卷号:111
  • 期号:23
  • 页码:8607-8612
  • DOI:10.1073/pnas.1407379111
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Use of the highly toxic and easily prepared rodenticide tetramethylenedisulfotetramine (TETS) was banned after thousands of accidental or intentional human poisonings, but it is of continued concern as a chemical threat agent. TETS is a noncompetitive blocker of the GABA type A receptor (GABAAR), but its molecular interaction has not been directly established for lack of a suitable radioligand to localize the binding site. We synthesized [14C]TETS (14 mCi/mmol, radiochemical purity >99%) by reacting sulfamide with H14CHO and s-trioxane then completion of the sequential cyclization with excess HCHO. The outstanding radiocarbon sensitivity of accelerator mass spectrometry (AMS) allowed the use of [14C]TETS in neuroreceptor binding studies with rat brain membranes in comparison with the standard GABAAR radioligand 4'-ethynyl-4-n-[3H]propylbicycloorthobenzoate ([3H]EBOB) (46 Ci/mmol), illustrating the use of AMS for characterizing the binding sites of high-affinity 14C radioligands. Fourteen noncompetitive antagonists of widely diverse chemotypes assayed at 1 or 10 {micro}M inhibited [14C]TETS and [3H]EBOB binding to a similar extent (r2 = 0.71). Molecular dynamics simulations of these 14 toxicants in the pore region of the 1{beta}2{gamma}2 GABAAR predict unique and significant polar interactions for TETS with 1T1' and {gamma}2S2', which are not observed for EBOB or the GABAergic insecticides. Several GABAAR modulators similarly inhibited [14C]TETS and [3H]EBOB binding, including midazolam, flurazepam, avermectin Ba1, baclofen, isoguvacine, and propofol, at 1 or 10 M, providing an in vitro system for recognizing candidate antidotes.
  • 关键词:neurotoxicity ; convulsant ; molecular modeling
国家哲学社会科学文献中心版权所有