谷氨酰胺
精氨酸
医学
瓜氨酸
一氧化氮
餐后
亮氨酸
氨基酸
限制
内科学
免疫系统
短肠综合征
内分泌学
生物化学
肠外营养
免疫学
化学
工程类
胰岛素
机械工程
作者
Luc Cynober,Christophe Moinard,Jean‐Pascal De Bandt
标识
DOI:10.1016/j.clnu.2010.07.006
摘要
Citrulline (CIT) is synthesized from arginine (ARG) and glutamine in enterocytes and metabolized by the kidneys into arginine, which is available for peripheral tissues. Thus CIT, rather than ARG, could be a limiting amino acid (AA) in situations of intestinal failure. This was verified in a rat model of short bowel syndrome. The effects of CIT were further tested in renutrition of malnourished rats and in healthy volunteers fed a hypoproteic diet. CIT supplementation improved protein synthesis (PS) and ARG availability more than ARG itself, which is explained by the fact that CIT, unlike ARG, is very efficiently transported into enterocytes and escapes hepatic uptake. Action of CIT on PS is mediated through the mTOR pathway. A key issue is why CIT should stimulate PS. CIT could be a counterpart of leucine, with leucine stimulating PS in the postprandial state, while CIT acts when protein intake is low or nil to maintain PS at a minimal level compatible with life. CIT could also be a safe way to deliver ARG to endothelial and immune cells, and can certainly prevent excessive uncontrolled nitric oxide production.
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