Silveira J E, Cirne B R
Comp Biochem Physiol A Comp Physiol. 1983;75(4):631-4. doi: 10.1016/0300-9629(83)90432-2.
Open-circuit voltage (PD) and short-circuit current (SCC) across toad skin were studied in in vivo conditions. An improved technique for fastening a lucite chamber on the abdominal region of the animal was developed. Saline bridges (230 mM NaCl in 4% agar solution) were placed subcutaneously to make the connections between the extracellular fluid and the half-cells. A clear relationship was observed between the electrical parameters and sodium transport by the skin, since PD and SCC were related to the sodium concentration of the bathing solution, and abolished by the presence of amiloride--a specific sodium transport inhibitor in epithelia. The initial control values of SCC in vivo were higher than those in vitro, which was attributed to hormonal stimulation. However, these high initial control values of SCC in vivo fell with time, reaching steady levels after a 2 hr period. Vasopressin failed to increase SCC in vivo when the external sodium concentration was 115 mM, being effective only when the sodium concentration was low (5 mM). On the other hand, in isolated preparations vasopressin significantly promoted an increase in both PD and SCC.
在体内条件下研究了蟾蜍皮肤的开路电压(PD)和短路电流(SCC)。开发了一种将有机玻璃腔固定在动物腹部区域的改进技术。皮下放置盐桥(4%琼脂溶液中的230 mM NaCl)以建立细胞外液与半电池之间的连接。观察到电参数与皮肤钠转运之间存在明确关系,因为PD和SCC与浴液中的钠浓度有关,并且上皮中特异性钠转运抑制剂氨氯吡脒的存在会消除这种关系。体内SCC的初始对照值高于体外,这归因于激素刺激。然而,体内SCC的这些高初始对照值随时间下降,在2小时后达到稳定水平。当外部钠浓度为115 mM时,血管加压素在体内未能增加SCC,仅在钠浓度低(5 mM)时有效。另一方面,在分离的制剂中,血管加压素显著促进了PD和SCC的增加。