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Inverse relation in the de novo arginase synthesis and nitric oxide production in murine and rat peritoneal macrophages in long-term cultures in vitro.

作者信息

Hrabák A, Temesi A, Csuka I, Antoni F

机构信息

First Department of Biochemistry, Semmelweis University Medical School, Budapest, Hungary.

出版信息

Comp Biochem Physiol B. 1992 Dec;103(4):839-45. doi: 10.1016/0305-0491(92)90202-3.

DOI:10.1016/0305-0491(92)90202-3
PMID:1478064
Abstract
  1. The de novo synthesis of arginase was much higher in murine than in rat peritoneal macrophages. This process was inhibited irreversibly by protein synthesis inhibitors and reversibly by glycolysis blockers. 2. Rat macrophages produce more nitric oxide (NO) than murine cells. NO production was inhibited by the inhibitors of protein synthesis or glycolysis. 3. The loading of macrophages by exogenous arginine for 24 hr in vitro resulted in the increase of arginase and nitrite in macrophages to different extents. 4. No great differences in lysozyme production was observed. 5. The proportion of arginine taken up and incorporated is contrasted in murine and rat macrophages.
摘要

相似文献

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Inverse relation in the de novo arginase synthesis and nitric oxide production in murine and rat peritoneal macrophages in long-term cultures in vitro.
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2
Arginine supply for nitric oxide synthesis and arginase is mainly exogenous in elicited murine and rat macrophages.在诱导的小鼠和大鼠巨噬细胞中,用于一氧化氮合成和精氨酸酶的精氨酸供应主要是外源性的。
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Comparison of substrate and inhibitor specificity of arginase and nitric oxide (NO) synthase for arginine analogues and related compounds in murine and rat macrophages.小鼠和大鼠巨噬细胞中精氨酸酶和一氧化氮(NO)合酶对精氨酸类似物及相关化合物的底物和抑制剂特异性比较。
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J Immunol. 2003 Nov 1;171(9):4561-8. doi: 10.4049/jimmunol.171.9.4561.

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2
Arginine metabolism: nitric oxide and beyond.精氨酸代谢:一氧化氮及其他
Biochem J. 1998 Nov 15;336 ( Pt 1)(Pt 1):1-17. doi: 10.1042/bj3360001.