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大鼠肝微粒体中叔丁基醌和叔丁基对苯二酚半醌阴离子自由基的形成。

Formation of the semiquinone anion radical from tert-butylquinone and from tert-butylhydroquinone in rat liver microsomes.

作者信息

Bergmann B, Dohrmann J K, Kahl R

机构信息

Institute of Physical and Theoretical Chemistry, Free University of Berlin, Germany.

出版信息

Toxicology. 1992 Sep;74(2-3):127-33. doi: 10.1016/0300-483x(92)90133-y.

Abstract

The tert-butylsemiquinone anion radical is formed from tert-butylhydroquinone and from tert-butylquinone in rat liver microsomes. In the presence of oxygen, the quinone and, less extensively, the hydroquinone induce excess production of superoxide in microsomes. It is concluded that autoxidation of the semiquinone formed from the quinone by microsomal enzyme activity is responsible for superoxide formation and that the hydroquinone enters the redox cycle via autoxidation. tert-Butylquinone induces injury of the hepatocyte plasma membrane. tert-Butylhydroquinone and tert-butylquinone are metabolites of the antioxidant butylated hydroxyanisole. The semiquinone-dependent superoxide formation may contribute to the toxic actions of butylated hydroxyanisole.

摘要

叔丁基半醌阴离子自由基由大鼠肝微粒体中的叔丁基对苯二酚和叔丁基醌形成。在有氧存在的情况下,醌以及程度稍低的对苯二酚会诱导微粒体中超氧化物的过量产生。得出的结论是,由微粒体酶活性使醌形成的半醌发生自氧化是超氧化物形成的原因,并且对苯二酚通过自氧化进入氧化还原循环。叔丁基醌会诱导肝细胞质膜损伤。叔丁基对苯二酚和叔丁基醌是抗氧化剂丁基化羟基茴香醚的代谢产物。半醌依赖性超氧化物的形成可能导致丁基化羟基茴香醚的毒性作用。

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