Yoshitomi K, Naruse M, Hanaoka K, Yamamura Y, Imai M, Kurokawa K
First Department of Internal Medicine, University of Tokyo, Japan.
Kidney Int Suppl. 1996 Jun;55:S177-82.
Recently we clarified the mechanism in which arginine-vasopressin (AVP) applied from the luminal side inhibits the basolateral Cl- conductance, which is stimulated by basolateral AVP. However, to prove that these vasopressin phenomena are expressed via receptor mediated actions, we examined the effect of specific V1 and V2 receptor antagonists, OPC-21268 and OPC-31260, respectively, on the electrical response to vasopressin in the rabbit CCD perfused in vitro. In the presence of the V2-antagonist, basolateral AVP caused only the activation of luminal Na+ conductance, indicating a V1 action. In the presence of the V1 antagonist, basolateral AVP caused the same biphasic responses in electrical parameters as cyclic AMP, representing a pure V2 action. On the other hand, a rise in cell Ca2+ in response to AVP was completely abolished in the presence of the V1-antagonist, but not by the V2-antagonist in the bath. These data confirm our earlier findings that rabbit CCD possesses both V1 and V2 receptors in the basolateral membrane. We conclude that electrical responses to AVP in the rabbit CCD are a complex of V1 and V2 receptor-mediated actions.
最近,我们阐明了从管腔侧施加的精氨酸加压素(AVP)抑制由基底外侧AVP刺激的基底外侧Cl-电导的机制。然而,为了证明这些加压素现象是通过受体介导的作用来表达的,我们分别研究了特异性V1和V2受体拮抗剂OPC-21268和OPC-31260对体外灌注的兔皮质集合管(CCD)中加压素电反应的影响。在存在V2拮抗剂的情况下,基底外侧AVP仅引起管腔Na+电导的激活,表明是V1作用。在存在V1拮抗剂的情况下,基底外侧AVP在电参数上引起与环磷酸腺苷相同的双相反应,代表纯V2作用。另一方面,在浴液中存在V1拮抗剂时,对AVP反应的细胞Ca2+升高完全被消除,但V2拮抗剂则没有这种作用。这些数据证实了我们早期的发现,即兔CCD在基底外侧膜中同时拥有V1和V2受体。我们得出结论,兔CCD中对AVP的电反应是V1和V2受体介导作用的复合体。