精氨酸酶
心肌保护
药理学
医学
缺血
封锁
再灌注损伤
一氧化氮
精氨酸
一氧化氮合酶
内科学
化学
生物化学
受体
氨基酸
作者
Christian Jung,Adrian Gonon,P.‐O. Sjöquist,Jon O. Lundberg,John Pernow
摘要
Inhibition of arginase protects from myocardial infarction by a mechanism that is dependent on NOS activity and bioavailability of NO by shifting arginine utilization from arginase towards NOS. These findings suggest that targeting of arginase is a promising future therapeutic strategy for protection against myocardial IR injury.
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