Koch T, Gloddek B, Gutzke S
Department of Otorhinolaryngology, Medizinische Hochschule, University of Hannover, FRG.
Hear Res. 1992 Nov;63(1-2):197-202. doi: 10.1016/0378-5955(92)90085-2.
The distribution of binding sites for atrial natriuretic peptide (ANP) has been examined in frozen sections of the guinea pig inner ear by means of autoradiography. The highest density was found in the stria vascularis of all cochlear turns. In membrane preparations of stria vascularis in vitro, the production of the second messenger cGMP was strongly stimulated by synthetic ANP in a dose dependent manner. Adenylate cyclase was neither stimulated nor inhibited by ANP, thus suggesting, that the binding sites coincide with an ANP receptor, which is coupled to guanylate cyclase but not negatively coupled to an adenylate cyclase molecule. The production of cyclic GMP could not be reduced by GDP-beta S, a strong inhibitor of the Gs protein. We conclude the existence of an ANP receptor-guanylate cyclase signal transfer system, similar to the beta 2 receptor-adenylate cyclase system in the inner ear, without coupling to a G protein. ANP might play a role in sodium and water regulation of the endolymph and might antagonize the action of vasopressin.
利用放射自显影技术,对豚鼠内耳冰冻切片中心房钠尿肽(ANP)结合位点的分布进行了研究。在所有耳蜗螺旋的血管纹中发现了最高密度的结合位点。在体外血管纹的膜制剂中,合成的ANP以剂量依赖的方式强烈刺激第二信使环磷酸鸟苷(cGMP)的产生。ANP既不刺激也不抑制腺苷酸环化酶,因此表明,这些结合位点与一种ANP受体一致,该受体与鸟苷酸环化酶偶联,但不与腺苷酸环化酶分子负偶联。GDP-β-S(一种Gs蛋白的强抑制剂)不能降低环磷酸鸟苷的产生。我们得出结论,存在一种ANP受体-鸟苷酸环化酶信号转导系统,类似于内耳中的β2受体-腺苷酸环化酶系统,且不与G蛋白偶联。ANP可能在内淋巴的钠和水调节中发挥作用,并可能拮抗血管加压素的作用。