Nipradilol induces vasodilation of canine isolated posterior ciliary artery via stimulation of the guanylyl cyclase-cGMP pathway

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• 作者：Kitaoka ; Yasushi ; Kumai ; Toshio ; Isenoumi ; Kazuyuki ; Kobayashi ; Shinichi ; Ueno ; Satoki
• 关键词：Ciliary artery ; Nitric oxide ; Cyclic GMP ; Nipradilol
• 刊名：Life Sciences
• 出版年：2002
• 期刊代码：62_00243205
• 类别：imm
• 出版时间：July 26, 2002
• 卷：71
• 期：10
• 页码：1115-1124
• 文件大小：230 K

摘要

We examined the effect of nipradilol on contraction of the posterior ciliary artery induced by high potassium or norepinephrine and on cyclic GMP (cGMP) levels in the posterior ciliary artery of dogs. Nipradilol caused dose-dependent relaxation of KCl-and norepinephrine-induced contractions of posterior ciliary artery. The relaxant effect of nipradilol on norepinephrine-contracted ciliary artery was significantly greater than that on KCl-contracted ciliary artery. In KCl-contracted ciliary artery, N^G-nitro-L-arginine methyl ester hydrochloride (L-NAME, 10⁻⁴ M) did not alter the relaxant effect of nipradilol, whereas 1H-1,2,4-oxadiazolo-4,3-a-quinoxalin-1-one (ODQ, 10⁻⁶ M) significantly inhibited this effect. Ethacrynic acid at 10⁻⁵ M, sulfasalazine at 10⁻⁴ M and S-decylglutathione at 10⁻⁴ M (glutathione S-transferase inhibitors) did not inhibit the relaxant effect of nipradilol. In addition, nipradilol produced dose-dependent increases in cGMP levels in the canine posterior ciliary artery. These findings indicate that nipradilol-induced vasorelaxation in the canine posterior ciliary artery occurs via stimulation of the guanylyl cyclase-cGMP pathway.