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AJP - Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. It is published 12 times a year (monthly) by the American Physiological Society, 9650 Rockville Pike, Bethesda MD 20814-3991. Copyright © 1997 by the American Physiological Society. ISSN: 0363-6143, ESSN: 1522-1563. Visit our website at http://www.the-aps.org/. of neuropeptide Y1 receptor function in SK-N-MC cells by nitric oxide . J. DOTSCH,l J. II.&ZE,l 0. BESTE,l J. BEHRENDT,2 W.-M. WEBER,â K. DITTRICH,l AND W. RASCHERl lDepartment of Pediatrics and 21nstitute of Animal Physiology, Justus-Liebig-Universittit, D-35385 Giessen, Germany Diitsch, J., J. H&me, 0. Beste, J. Behrendt, W.-M. Weber, K. Dittrich, and W. Rascher. of neuropeptide Y1 receptor function in SK-N-MC cells by nitric oxide. Am. J. Physiol. 273 (Cell Physiol. 42): C618-C621, 1997.The neuropeptide Y1 receptor () predominantly mediates the vasoconstrictor effects of NPY in smooth muscle cells. The present experiments were planned to study the direct influence of the vasodilator nitric oxide (NO) on NPY1receptor function. SK-N-MC and CHP-234 cells expressing Yi and YB receptor, respectively, were incubated with the NO donors sodium nitroprusside (SNP), 3-morpholinosydnonimine (SIN-l), and S-nitroso-N-acetyl-penicillamine (SNAP). Receptor binding, Y1-receptor mRNA expression rthern blot, and adenosine 3â,5â-cyclic monophosphate (CAMP) and
AJP - Cell Physiology – The American Physiological Society
Published: Aug 1, 1997
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