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Arginase Activities and Global Arginine Bioavailability in Wild-Type and ApoE-Deficient Mice: Responses to High Fat and High Cholesterol Diets

机译:野生型和ApoE缺陷型小鼠的精氨酸酶活性和全球精氨酸的生物利用度:对高脂肪和高胆固醇饮食的反应

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Increased catabolism of arginine by arginase is increasingly viewed as an important pathophysiological factor in cardiovascular disease, including atherosclerosis induced by high cholesterol diets. Whereas previous studies have focused primarily on effects of high cholesterol diets on arginase expression and arginine metabolism in specific blood vessels, there is no information regarding the impact of lipid diets on arginase activity or arginine bioavailability at a systemic level. We, therefore, evaluated the effects of high fat (HF) and high fat-high cholesterol (HC) diets on arginase activity in plasma and tissues and on global arginine bioavailability (defined as the ratio of plasma arginine to ornithine + citrulline) in apoE−/− and wild-type C57BL/6J mice. HC and HF diets led to reduced global arginine bioavailability in both strains. The HC diet resulted in significantly elevated plasma arginase in both strains, but the HF diet increased plasma arginase only in apoE−/− mice. Elevated plasma arginase activity correlated closely with increased alanine aminotransferase levels, indicating that liver damage was primarily responsible for elevated plasma arginase. The HC diet, which promotes atherogenesis, also resulted in increased arginase activity and expression of the type II isozyme of arginase in multiple tissues of apoE−/− mice only. These results raise the possibility that systemic changes in arginase activity and global arginine bioavailability may be contributing factors in the initiation and/or progression of cardiovascular disease.
机译:精氨酸酶增加的精氨酸分解代谢被越来越多地视为心血管疾病的重要病理生理因素,包括高胆固醇饮食诱发的动脉粥样硬化。尽管先前的研究主要集中于高胆固醇饮食对特定血管中精氨酸酶表达和精氨酸代谢的影响,但尚无关于脂质饮食对全身水平精氨酸酶活性或精氨酸生物利用度影响的信息。因此,我们评估了高脂(HF)和高脂高胆固醇(HC)饮食对apoE中血浆和组织中精氨酸酶活性以及全球精氨酸生物利用度(定义为血浆精氨酸与鸟氨酸+瓜氨酸的比率)的影响。 -/-和野生型C57BL / 6J小鼠。 HC和HF饮食导致两种菌株的整体精氨酸生物利用度降低。 HC饮食在两种品系中均导致血浆精氨酸酶显着升高,而HF饮食仅在apoE-/-小鼠中增加血浆精氨酸酶。血浆精氨酸酶活性升高与丙氨酸转氨酶水平升高密切相关,表明肝脏损害是血浆精氨酸酶升高的主要原因。仅促进apoE-/-小鼠多个组织的HC饮食,促进动脉粥样硬化的形成,还导致精氨酸酶活性的提高和精氨酸酶II型同工酶的表达。这些结果增加了精氨酸酶活性的系统性变化和整体精氨酸生物利用度可能是心血管疾病的开始和/或发展的促成因素的可能性。

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