半胱氨酸
谷胱甘肽
胱氨酸
半胱氨酸代谢
牛磺酸
生物化学
细胞外
新陈代谢
细胞内
氨基酸
化学
分解代谢
半胱氨酸
酶
作者
Jie Yin,Wenkai Ren,Guan Yang,Jielin Duan,Xingguo Huang,Rejun Fang,Chong-Yong Li,Yuying Li,Yulong Yin,Yongqing Hou,Sung Woo Kim,Guoyao Wu
标识
DOI:10.1002/mnfr.201500031
摘要
l ‐Cysteine is a nutritionally semiessential amino acid and is present mainly in the form of l ‐cystine in the extracellular space. With the help of a transport system, extracellular l ‐cystine crosses the plasma membrane and is reduced to l ‐cysteine within cells by thioredoxin and reduced glutathione (GSH). Intracellular l ‐cysteine plays an important role in cellular homeostasis as a precursor for protein synthesis, and for production of GSH, hydrogen sulfide (H 2 S), and taurine. l ‐Cysteine‐dependent synthesis of GSH has been investigated in many pathological conditions, while the pathway for l ‐cysteine metabolism to form H 2 S has received little attention with regard to prevention and treatment of disease in humans. The main objective of this review is to highlight the metabolic pathways of l ‐cysteine catabolism to GSH, H 2 S, and taurine, with special emphasis on therapeutic and nutritional use of l ‐cysteine to improve the health and well‐being of animals and humans.
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