Kachadorian W A, Levine S D, Wade J B, Di Scala V A, Hays R M
J Clin Invest. 1977 Mar;59(3):576-81. doi: 10.1172/JCI108673.
It has been previously demonstrated with freeze-fracture electron microscopy that vasopressin induces specific structural alterations of the luminal membrane of granular cells from toad urinary bladder in a dose-dependent fashion. These alterations consist of aggregated intramembranous particles and are observed both in the presence and absence of an osmotic gradient. We examined the effect of methohexital, a selective inhibitor of vasopressin-stimulated water flow, and the effect of phloretin, a selective inhibitor of urea permeability, on the structure of the granular cell luminal membrane. Methohexital treatment of the vasopressin-stimulated toad bladder reduced both the osmotic water flow and vasopressin-induced alterations of membrane structure to the same extent. Phloretin reduced urea permeability but not water flow or particle aggregation. Since neither agent affects vasopressin-stimulated sodium movement, these findings indicate that the phenomenon of particle aggregation is specifically related to vasopressin-induced water permeability and not to changes in urea or sodium permeability.
先前通过冷冻断裂电子显微镜已证明,血管加压素以剂量依赖方式诱导蟾蜍膀胱颗粒细胞管腔膜的特定结构改变。这些改变包括聚集的膜内颗粒,且在存在和不存在渗透梯度的情况下均能观察到。我们研究了美索比妥(一种血管加压素刺激的水流的选择性抑制剂)以及根皮素(一种尿素通透性的选择性抑制剂)对颗粒细胞管腔膜结构的影响。用美索比妥处理血管加压素刺激的蟾蜍膀胱,可同等程度地降低渗透水流和血管加压素诱导的膜结构改变。根皮素降低了尿素通透性,但未影响水流或颗粒聚集。由于这两种药物均不影响血管加压素刺激的钠转运,这些发现表明颗粒聚集现象与血管加压素诱导的水通透性特异性相关,而与尿素或钠通透性的变化无关。