期刊
PHYSIOLOGICAL REVIEWS
卷 98, 期 2, 页码 641-665出版社
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physrev.00037.2016
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资金
- National Heart, Lung, and Blood Institute Grant [RO1HL070215]
- National Eye Institute [RO1EY011766]
- National Cancer Institute [RO1CA18485]
- American Heart Association [13SDG174100007, 11SDG7440088]
- United States Department of Veterans Affairs [I01BX003221]
- Department of Veterans Affairs
- NATIONAL CANCER INSTITUTE [R01CA184185] Funding Source: NIH RePORTER
- NATIONAL EYE INSTITUTE [R01EY011766] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R24DK094765] Funding Source: NIH RePORTER
- Veterans Affairs [I01BX001233, I01BX003221] Funding Source: NIH RePORTER
The arginase enzyme developed in early life forms and was maintained during evolution. As the last step in the urea cycle, arginase cleaves L-arginine to form urea and L-ornithine. The urea cycle provides protection against excess ammonia, while L-ornithine is needed for cell proliferation, collagen formation, and other physiological functions. In mammals, increases in arginase activity have been linked to dysfunction and pathologies of the cardiovascular system, kidney, and central nervous system and also to dysfunction of the immune system and cancer. Two important aspects of the excessive activity of arginase may be involved in diseases. First, overly active arginase can reduce the supply of L-arginine needed for the production of nitric oxide (NO) by NO synthase. Second, too much L-ornithine can lead to structural problems in the vasculature, neuronal toxicity, and abnormal growth of tumor cells. Seminal studies have demonstrated that increased formation of reactive oxygen species and key inflammatory mediators promote this pathological elevation of arginase activity. Here, we review the involvement of arginase in diseases affecting the cardiovascular, renal, and central nervous system and cancer and discuss the value of therapies targeting the elevated activity of arginase.
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