Ardizzone C, Lippe C
Arch Int Physiol Biochim. 1985 Jun;93(2):135-41. doi: 10.3109/13813458509079599.
Maximal doses of vasopressin increase the permeability of the skins of Bufo bufo and Rana esculenta to urea, ethylene glycol, glycerol, erythritol, beta-alanine, leaving virtually unmodified that of mannitol and antipyrine. These results demonstrate that the response to vasopressin is quite different in amphibian skins as compared to the bladders. A careful analysis of the effects of vasopressin on non-electrolyte permeability as a function of their molecular weight demonstrates that hormone elicits the formation of pores with a diameter inferior to 4 A. Under vasopressin treatment the skins exhibit a selectivity for polyhydroxylated molecules as compared to urea and beta-alanine. This selectivity is not due to active of facilitated transport and is not impaired by phloretin or DTNB which selectively blocks the permeability of urea or ethylene glycol in erythrocytes. It is proposed that the site of such selectivity is located in other plasma membranes of the epithelium.
血管加压素的最大剂量会增加蟾蜍和食用蛙皮肤对尿素、乙二醇、甘油、赤藓醇、β-丙氨酸的通透性,而对甘露醇和安替比林的通透性几乎没有影响。这些结果表明,与膀胱相比,两栖动物皮肤对血管加压素的反应有很大不同。对血管加压素对非电解质通透性的影响(作为分子量的函数)进行仔细分析表明,该激素会引发直径小于4埃的孔的形成。在血管加压素处理下,与尿素和β-丙氨酸相比,皮肤对多羟基化分子具有选择性。这种选择性不是由于主动转运或易化转运,并且不受根皮素或二硫硝基苯甲酸(DTNB)的影响,后者会选择性地阻断红细胞中尿素或乙二醇的通透性。有人提出,这种选择性的部位位于上皮细胞的其他质膜中。