Ando Y, Asano Y
Division of Nephrology, Jichi Medical School, Tochigi, Japan.
Am J Physiol. 1995 Jun;268(6 Pt 2):F1093-101. doi: 10.1152/ajprenal.1995.268.6.F1093.
We have previously found that arginine vasopressin (AVP) acts not only from the basolateral side but also from the luminal side of the rabbit cortical collecting duct (CCD). In the present study, we examined whether prostaglandin E2 (PGE2), another classic and potent modulator of the collecting duct functions, exerts luminal actions in the rabbit CCD perfused in vitro. Although luminal prostaglandin I2 was inert, luminal PGE2 (> 1 nM) induced transient hyperpolarization of transepithelial voltage followed by sustained depolarization in a dose-dependent manner. This action was preserved in the presence of basolateral PGE2, luminal AVP, or luminal BaCl2, but abolished by basolateral ouabain or luminal amiloride. Furthermore, unlike luminal AVP, luminal PGE2 suppressed Na transport and increased osmotic water permeability. The present study suggests that PGE2, similar to AVP but in a different fashion, modulates transepithelial transports from both luminal and basolateral sites in the CCD in vivo.
我们之前发现,精氨酸加压素(AVP)不仅可从兔皮质集合管(CCD)的基底外侧发挥作用,还可从管腔侧发挥作用。在本研究中,我们检测了另一种对集合管功能具有经典且强效调节作用的物质——前列腺素E2(PGE2),是否在体外灌注的兔CCD中发挥管腔作用。尽管管腔前列腺素I2无活性,但管腔PGE2(>1 nM)可诱导跨上皮电压短暂超极化,随后以剂量依赖方式持续去极化。在存在基底外侧PGE2、管腔AVP或管腔BaCl2的情况下,该作用得以保留,但被基底外侧哇巴因或管腔阿米洛利消除。此外,与管腔AVP不同,管腔PGE2可抑制钠转运并增加渗透水通透性。本研究表明,PGE2与AVP类似,但方式不同,在体内可从管腔和基底外侧两个部位调节CCD中的跨上皮转运。