作者: Osamu Yasuda , Yoshiharu Chijiiwa , Yasuaki Motomura , Toshiaki Ochiai , Hajime Nawata
DOI: 10.1016/S0167-0115(99)00101-9
关键词: Cyclase 、 Protein kinase A 、 NPR1 、 Myocyte 、 Atrial natriuretic peptide 、 Internal medicine 、 Brain natriuretic peptide 、 NPR2 、 Endocrinology 、 Natriuretic peptide 、 Biology
摘要: Guinea pig caecal circular smooth muscle cells were used to determine whether brain natriuretic peptide (BNP) can inhibit the contractile response produced by cholecystokinin-octapeptide (CCK-8). In addition, we examined effect of an inhibitor cAMP-dependent protein kinase, particulate or soluble guanylate cyclase, atrial (ANP) antagonist (ANP 1-11), and selective receptor protection on BNP-induced relaxation these cells. The BNP cAMP formation was also examined. inhibited CCK-8 in a dose-response manner, with IC50 value 8.5 nM, stimulated production cAMP. kinase cyclase significantly BNP. contrast, did not have any significant ANP 1-11 but partially where binding sites protected completely preserved inhibitory ANP, both This study demonstrates that induces via coupled distinct adenylate cyclase.