Nitric oxide-induced ciliary muscle relaxation during contraction with endothelin-1 is mediated through elevation of cyclic GMP

References

• Haefliger, I. O., Zschauer, A. and Anderson, D. R. (1994) Relaxation of retinal pericyte contractile tone through the nitric oxide-cyclic guanosine monophosphate pathway. Invest. Ophthalmol. Vis. Sci. 35, 991–997.
   PubMed Web of Science ®Google Scholar
• Tamm, E. R., Flugel-Koch, C., Mayer, B. and Lutjen-Drecoll, E. (1995) Nerve cells in the human ciliary mus-cle: ultrastructural and immunocytochemical characteriza-tion. Invest. Ophthalmol. Vis. Sci 36, 414–426.
   Google Scholar
• Yamamoto, R., Bredt, D. S., Snyder, S. H. and Stone, R. A. (1993) The localization of nitric oxide synthase in the rat eye and related cranial ganglia. Neuroscience, 54, 189–200.
   PubMed Web of Science ®Google Scholar
• Geyer, O., Podos, S. M. and Mittag, T. W. (1993) Nitric oxide synthase: distribution and biochemical properties of the enzyme in the bovine eye. Invest. Ophthalmol. Vis. Sci 34, 826–832.
   Google Scholar
• Nathanson, J. A. and McKee, M. (1995) Identification of an extensive system of nitric oxide-producing cells in the ciliary muscle and outflow pathway of the human eye. Invest. Ophthalmol. Vis. Sci. 36, 1765–1773.
   PubMed Web of Science ®Google Scholar
• Nathanson, J. A. and McKee, M. (1995) Alteration of ocu-lar nitric oxide synthase in human glaucoma. Invest. Oph-thalmol. Vis. Sci. 36, 1774–1784.
   PubMed Web of Science ®Google Scholar
• Yanagisawa, M., Kurihara, H., Tomobe, Y., Kobayashi, M., Mitsui, Y., Yazaki, Y, Goto, K. and Masaki, T. (1988) Endothelin: a novel potent vasoconstrictor peptide by vas-cular endothelial cells. Nature, 322, 411–415.
   Web of Science ®Google Scholar
• Haefliger, I. O., Flammer, J. and Liischer, T. F. (1992) Nitric oxide and endothelin-1 are important regulators of human ophthalmic artery. Invest. Ophthalmol. Vis. Sci 33, 2340–2343.
   PubMed Web of Science ®Google Scholar
• Erickson-Lamy, K. A., Korbmacher, C., Schuman, J. S. and Nathanson, J. A. (1991) Invest. Ophthalmol. Vis. Sci 32, 492–495.
   Google Scholar
• Millar, C., Poyer, J. F., Gabelt, B. T. and Kaufman, P. L. (1995) Endothelin subtypes: effect on isolated rhesus monkey ciliary muscle. I PharmacoL Exp. Ther. 275, 1143–1147.
   PubMed Web of Science ®Google Scholar
• Azuma, H., Hamasaki, H., Sato, J., Isotani, E., Obayashi, S. and Matsubara, O. (1995) Different localization of ETA and ETB receptors in the hyperplastic vascular wall. Cardiovasc. PharmacoL 25, 802–809.
   PubMed Web of Science ®Google Scholar
• Abdel-Latif, A. A. and Zhang, Y. (1991) Species differ-ences in the effects of endothelin-1 on myo-inositol tri-phosphate accumulation, cGMP formation and contraction of isolated iris sphincter of rabbit and other species. Invest. Ophthalmol. Vis. Sci. 32, 2432–2438.
   Google Scholar
• Kamikawatoko, S., Tokoro, T., Azuma, H., Hamasaki, H. and Ishida, A. (1995) Effect of endothelin-1 on isolated bovine ciliary muscle. Exp. Eye Res. 61, 559–564.
   PubMed Web of Science ®Google Scholar
• Matsumoto, S., Yorio, T., Magnino, P. E., DeSantis, L. and Pang, I. (1996) Endothelin-induced changes of second messengers in cultured human ciliary muscle cells. Invest. Ophthalmol. Vis. Sci 37, 1058–1066.
   PubMed Web of Science ®Google Scholar
• Abdel-Latif, A. A., Yousufzai, S. Y K., El-Mowafy, A. M. and Ye, Z. (1996) Prostaglandins mediates the stimulatory effects of endothelin-1 on cyclic adenosine monophos-phate accumulation in ciliary smooth muscle isolated from bovine, cat and other mammalian species. Invest. Ophthal-mol. Vis. Sci. 37, 328–338.
   Google Scholar
• Boulanger, C. and Liischer, T. F. (1990) Release of endo-thelin from the porcine aorta, inhibition by endothelium-derived nitric oxide. J. Clin. Invest. 85, 587–590.
   PubMed Web of Science ®Google Scholar
• Owada, A., Tomita, K., Terada, Y., Sakamoto, H., Nonogu-chi, H. and Marumo, F. (1994) Endothelin (ET)-3 stimu-lates cyclic guanosine 3',5 '-monophosphate production via ETB receptor by producing nitric oxide in isolated rat glomerulus, and in cultured rat mesangial cells. J. Clin. Invest. 93, 556–563.
   PubMed Web of Science ®Google Scholar
• Ignarro, L. J., Harbinson, R. G., Wood, K. S. and Kado-witz, P. J. (1986) Dissimilarities between methylene blue and cyanide on relaxation and cyclic GMP formation in endothelium-intact intrapulmonary artery caused by nitro- gen oxide-containing vasodilators and acetylcholine. .1 PharmacoL Exp. Ther 236, 30–36.
   Google Scholar
• Ignarro, L. J. and Kadowitz, P. J. (1985) The pharmacolog-ical and physiological role of cyclic GMP in vascular smooth muscle relaxation. Ann. Rev. PharmacoL ToxicoL 25, 171–191.
   PubMed Web of Science ®Google Scholar
• Lowry, O. H., Rosebrough, N. J., Farr, A. L. and Randall, R. J. (1951) Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193, 265–275.
   PubMed Web of Science ®Google Scholar
• Kobayashi, Y. and Hattori, K. (1990) Nitroarginine inhibits endothelium-derived relaxation. Jpn. I PharmacoL 52, 167–169.
   PubMedGoogle Scholar
• Azuma, H., Masuda, H., Sato, J., Niwa, K. and Tokoro, T. (1997) A possible role of endogenous inhibitors for nitric oxide synthesis in the bovine ciliary muscle. Exp. Eye Res. In Press.
   Google Scholar
• Akaike, T., Yoshida, M., Miyamoto, Y., Sato, K., Kohno, M., Sakamoto, K., Miyazaki, K., Ueda, S. and Maeda, H. (1993) Antagonistic action of imidazolineoxyl N-oxide against endothelium-derived relaxing factor/NO through a radical reaction. Biochemistry, 32, 827–832.
   PubMed Web of Science ®Google Scholar
• Gryglewski, R. J., Palmer, R. M. J. and Moncada, S. (1986) Superoxide anion is involved in the breakdown of endothe-lium-derived vascular relaxing factor. Nature, 320,454–456.
   Google Scholar
• Kowulak, E. A., Seth, P. and Fung, H. (1992) Metabolic activation of sodium nitroprusside to nitric oxide in vascu-lar smooth muscle. ./. PharmacoL Exp. Ther. 262, 916–922.
   Google Scholar
• Wiederholt, W., Sturm, A. and Lepple-Wienhues, A. (1994) Relaxation of trabecular meshwork and ciliary muscle by release of nitric oxide. Invest. Ophthalmol. Vis. Sci. 35, 2512–2520.
   Google Scholar
• Gryglewski, R. J., Zemwicz, A., Salvemini, D., Teylor, G. W. and Vane, J. R. (1992) Modulation of the pharmaco-logical actions of nitrosodilators by methylene blue and pyocianin. Br J. PharmacoL 106, 838–845.
   Google Scholar
• Koesling, D., Bohme, E. and Schultz, G. (1991) Guanylate cyclase, a growing family of single-transducing enzymes. FASEB J. 5,2785–2791.
   PubMedGoogle Scholar
• Marczin, N., Ryan, U. S. and Catravas, J. D. (1992) Meth-ylene blue inhibits nitrosodilator and endothelium-derived relaxing factor-induced cGMP accumulation in cultured pulmonary arterial smooth muscle cells via generation of superoxide anion. J. PharmacoL Exp. Ther 263, 170–179.
   PubMed Web of Science ®Google Scholar
• Snyder, G. L., Girault, J. A., Chen, J. Y. C., Czernik, A. J., Kebabian, J. W., Nathanson, J. A. and Greengard, P. (1992) Phosphorylation of DARP-32 and protein phosphatase inhibitor-1 in rat choroid plexus: regulation by factors other than dopamine. Neurosci. 12, 3071–3083.
   Google Scholar
• McKee, M., Scavone, C. and Nathanson, J. A. (1994) Nitric oxide, cGMP and hormone regulation of active sodium transport. Proc. Natl. Acad. Sci USA, 91, 12056–12060.
   PubMed Web of Science ®Google Scholar
• Nathanson, J. A. (1988) Direct application of a guanylate cyclase activator lowers intraocular pressure. Eur. J. Phar-macoL 147, 155–156.
   PubMed Web of Science ®Google Scholar
• Nathanson, J. A. (1992) Nitrosovasodilators as a new class of ocular hypotensive agents. J. Pharmacol. Exp. Ther 260, 956–965.
   PubMed Web of Science ®Google Scholar
• Nathanson, J. A. (1988) Guanylyl cyclase activator: effects on ciliary process cyclic GMP metabolism and intraocular pressure. Invest. Ophthalmol. Vis. Sci 29, 323–325.
   Google Scholar
• Pussard, G., Gascard, J. P., Gorenne, I., Labat, C., Norel, X., Dulmet, E. and Brink, C. (1995) Endothelin-1 modu-lates cyclic GMP production and relaxation in human pul-monary vessels. J. Pharmacol. Exp. Ther. 274, 969–975.
   Google Scholar
• Becker, B. (1990) Topical 8-bromo cyclic GMP lowers intraocular pressure in rabbits. Invest. Ophthalmol. Js. Sci. 31, 1647–1649.
   PubMed Web of Science ®Google Scholar