Regulation of intracellular xanthine oxidase by endothelial-derived nitric oxide

被引:81
作者
Cote, CG [1 ]
Yu, FS [1 ]
Zulueta, JJ [1 ]
Vosatka, RJ [1 ]
Hassoun, PM [1 ]
机构
[1] TUFTS UNIV, DIV PULM & CRIT CARE,NEW ENGLAND MED CTR,SCH MED, DEPT MED, BOSTON, MA 02111 USA
关键词
N-G-nitro-L-arginine methyl ester; hypoxia; L-arginine; nitric oxide synthase;
D O I
10.1152/ajplung.1996.271.5.L869
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We have previously shown that nitric oxide (NO) donors, such as nitrosoglutathione, inhibit endothelial cell (EC) xanthine dehydrogenase (XD)/xanthine oxidase (XO) activity. The purpose of this study was to assess whether endothelial-derived NO plays any role in the regulation of intracellular XD/XO. We exposed rat pulmonary microvascular EC to L-arginine (precursor of NO) or inhibitors of nitric oxide synthase (NOS), i.e., N-G-nitro-L-arginine methyl esther (L-NAME) and N-G-nitro-L-arginine, in conditions of normoxia, hypoxia, and hypoxia followed by reoxygenation. Hypoxia alone caused a 1.9- and a 6.6-fold increase in XO and a 5-fold increase in XO + XD activities after 24 and 48 h of exposure, respectively. The combination of hypoxia and L-NAME (300 mu M) treatment amounted at 48 h to a 10- and 7.5-fold increase in XO and XO + XD activities, respectively, compared with normoxic untreated cells. L-NAME also prevented the decline in XD/XO activity that occurred in untreated EC after hypoxia-reoxygenation. On the other hand, treatment with L-arginine caused a dose-dependent decrease in XD/XO activity in hypoxic EC compared with cells provided with L-arginine-free medium. In separate experiments, we assessed the role of L-arginine supplementation on the in vivo regulation of lung XD/XO by exposing male adult Sprague-Dawley rats for a period of 5 days to a hypoxic hypobaric atmosphere (0.5 atm). Exposure to hypoxia produced a significant increase in lung tissue XO activity and an increase in the ratio of XO to XD. L-Arginine supplementation in the drinking water prevented the increase in lung XO and the XO-to-XD ratio in hypoxic rats and caused a significant decrease in XO and XD in rats exposed to normoxia. In conclusion, this study suggests that endogenous NO has a significant role in the regulation of XD/XO both in vitro and in vivo. By inhibiting XD/XO activity, NO may have a modulating effect in conditions of hypoxia and hypoxia-reoxygenation, where this enzyme is thought to be important.
引用
收藏
页码:L869 / L874
页数:6
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