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Nitrone spin-traps block calcium channels and induce pulmonary artery relaxation independent of free radicals.

作者信息

Anderson D E, Yuan X J, Tseng C M, Rubin L J, Rosen G M, Tod M L

机构信息

Department of Medicine, University of Maryland School of Medicine, Baltimore.

出版信息

Biochem Biophys Res Commun. 1993 Jun 30;193(3):878-85. doi: 10.1006/bbrc.1993.1707.

DOI:10.1006/bbrc.1993.1707
PMID:8391809
Abstract

Free radicals react with nitrones to form stable nitroxides which can be identified by ESR spectroscopy. Unfortunately, little is known regarding the pharmacological properties of these compounds. In this study, three commonly used nitrones, 5,5-dimethylpyrroline-N-oxide (DMPO), alpha-phenyl-tert-butylnitrone (PBN), and alpha-(4-pyridyl 1-oxide)-N-tert-butylnitrone (POBN), were found to induce relaxation of preconstricted isolated rat pulmonary artery rings. Additional experiments with PBN indicated that vasorelaxation could not be attributed to production of endothelial derived factors, prostaglandins, or free radicals. Patch-clamp techniques revealed reversible calcium channel blockade with PBN at a concentration below that needed to detect free radicals. Calcium channel blockade probably accounts for the vasorelaxation observed in the isolated ring preparations described here, and should be considered when using nitrone spin-traps both in in vivo and clinical studies.

摘要

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引用本文的文献

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