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华法林会导致大鼠动脉和心脏瓣膜的弹性层迅速钙化。

Warfarin causes rapid calcification of the elastic lamellae in rat arteries and heart valves.

作者信息

Price P A, Faus S A, Williamson M K

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093-0368, USA.

出版信息

Arterioscler Thromb Vasc Biol. 1998 Sep;18(9):1400-7. doi: 10.1161/01.atv.18.9.1400.

Abstract

High doses of warfarin cause focal calcification of the elastic lamellae in the media of major arteries and in aortic heart valves in the rat. Aortic calcification was first seen after 2 weeks of warfarin treatment and progressively increased in density at 3, 4, and 5 weeks of treatment. By 5 weeks, the highly focal calcification of major arteries could be seen on radiographs and by visual inspection of the artery. The calcification of arteries induced by warfarin is similar to that seen in the matrix Gla protein (MGP)-deficient mouse, which suggests that warfarin induces artery calcification by inhibiting gamma-carboxylation of MGP and thereby inactivating the putative calcification-inhibitory activity of the protein. Warfarin treatment markedly increased the levels of MGP mRNA and protein in calcifying arteries and decreased the level of MGP in serum. Warfarin treatment did not affect bone growth, overall weight gain, or serum calcium and phosphorus levels, and, because of the concurrent administration of vitamin K, prothrombin times and hematocrits were normal. The results indicate that the improved warfarin plus vitamin K treatment protocol developed in this study should provide a useful model to investigate the role of MGP in preventing calcification of arteries and heart valves.

摘要

高剂量华法林会导致大鼠主要动脉中膜的弹性膜以及主动脉心脏瓣膜出现局灶性钙化。华法林治疗2周后首次出现主动脉钙化,且在治疗3、4和5周时钙化密度逐渐增加。到5周时,通过X光片以及对动脉的肉眼观察,可看到主要动脉出现高度局灶性钙化。华法林诱导的动脉钙化与基质γ-羧基谷氨酸蛋白(MGP)缺陷小鼠中所见的钙化相似,这表明华法林通过抑制MGP的γ-羧化作用,从而使该蛋白假定的钙化抑制活性失活,进而诱导动脉钙化。华法林治疗显著增加了钙化动脉中MGP的mRNA和蛋白水平,并降低了血清中MGP的水平。华法林治疗不影响骨骼生长、总体体重增加或血清钙和磷水平,并且由于同时给予了维生素K,凝血酶原时间和血细胞比容均正常。结果表明,本研究中开发的改进型华法林加维生素K治疗方案应能为研究MGP在预防动脉和心脏瓣膜钙化中的作用提供一个有用的模型。

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