期刊
BIOCHEMICAL JOURNAL
卷 456, 期 -, 页码 47-54出版社
PORTLAND PRESS LTD
DOI: 10.1042/BJ20130639
关键词
gamma-glutamyl carboxylase; NAD(P)H quinone oxidoreductase 1 (NQO1); NRH:quinone oxidoreductase 2 (NQO2); vitamin K; vitamin K epoxide reductase (VKOR); warfarin
资金
- National Institutes of Health [HL077740]
- Janet and Jim Glass JGP Postdoctoral Research Fellowship Award
- Hemophilia of Georgia
NQ01 [NAD(P)H quinone oxidoreductase 1; also known as DT-diaphorase] is a cytosolic enzyme that catalyses the two-electron reduction of various quinones including vitamin K. The enzyme may play a role in vitamin K metabolism by reducing vitamin K to vitamin K hydroquinone for utilization in the post-translational gamma-glutamyl carboxylation reactions required by several proteins involved in blood coagulation. The aim of the present study was to assess the contribution of NQ01 to vitamin K reduction and haemostasis in an in vivo model. We examined the contribution of NQ01 to haemostasis by examining survival rates in mice poisoned with the anticoagulant warfarin. Supraphysiological amounts of vitamin K sufficiently reversed the effects of warfarin in both wild-type and NQ01-deficient mice. Additionally, vitamin K reductase activities distinct from VKOR (vitamin K epoxide reductase) and NQ01 were measured in vitro from both wild-type and NQ01-defecient mice. The results of the present study suggest that NQ01 does not play a major role in the production of vitamin K hydroquinone and supports the existence of multiple vitamin K reduction pathways. The properties of a NAD(P)H-dependent vitamin K reductase different from NQ01 are described.
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