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Anti-inflammatory glucocorticoids inhibit the induction by endotoxin of nitric oxide synthase in the lung, liver and aorta of the rat.

作者信息

Knowles R G, Salter M, Brooks S L, Moncada S

机构信息

Wellcome Research Laboratories, Beckenham, Kent, U.K.

出版信息

Biochem Biophys Res Commun. 1990 Nov 15;172(3):1042-8. doi: 10.1016/0006-291x(90)91551-3.

DOI:10.1016/0006-291x(90)91551-3
PMID:1700903
Abstract

The induction by endotoxin of Ca2(+)-independent nitric oxide (NO) synthase in the lung and liver of the rat was prevented by the glucocorticoids dexamethasone and cortisol but not by progesterone. The activity of the constitutive Ca2(+)-dependent NO synthase in the brain and the aorta was not affected by treatment with either endotoxin or glucocorticoids. In the aorta a Ca2(+)-independent NO synthase was also found following endotoxin treatment of rats, and this induction was likewise prevented by dexamethasone. The Ca2(+)-dependent NO synthase in the aorta was located in the vascular endothelium, whereas the Ca2(+)-independent enzyme was predominantly located in the vascular smooth muscle layer. Inhibition of induction of the Ca2(+)-independent NO synthase in vivo may underlie some of the physiological and pharmacological effects of the anti-inflammatory glucocorticoids.

摘要

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1
Anti-inflammatory glucocorticoids inhibit the induction by endotoxin of nitric oxide synthase in the lung, liver and aorta of the rat.
Biochem Biophys Res Commun. 1990 Nov 15;172(3):1042-8. doi: 10.1016/0006-291x(90)91551-3.
2
Differential induction of brain, lung and liver nitric oxide synthase by endotoxin in the rat.内毒素对大鼠脑、肺和肝一氧化氮合酶的差异诱导作用
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7
Cytokines, endotoxin, and glucocorticoids regulate the expression of inducible nitric oxide synthase in hepatocytes.细胞因子、内毒素和糖皮质激素调节肝细胞中诱导型一氧化氮合酶的表达。
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Br J Pharmacol. 1993 Mar;108(3):786-92. doi: 10.1111/j.1476-5381.1993.tb12879.x.

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