Fujimoto M, Hagiwara N, Kubota T, Kotera K
Department of Physiology, Osaka Medical College, Japan.
Jpn J Physiol. 1988;38(5):619-41. doi: 10.2170/jjphysiol.38.619.
Using a direct cellular micropuncture technique with double-barreled ion-selective microelectrodes, we investigated the effect of dibutyryl-cyclic AMP (db-cAMP) on the membrane potential and the transport of Na+, K+, and H+ in doubly-perfused bullfrog proximal tubules. The peritubular membrane potential difference (EM) and the intracellular K+, Na+ activities ((K)i, (Na)i) or intracellular and luminal pH were monitored continuously after peritubular administration of db-cAMP (10(-3)-10(-4)M).
我们使用双管离子选择性微电极的直接细胞微穿刺技术,研究了二丁酰环磷腺苷(db-cAMP)对双灌注牛蛙近端小管膜电位以及钠、钾、氢离子转运的影响。在向肾小管周围给予db-cAMP(10⁻³ - 10⁻⁴M)后,持续监测肾小管周围膜电位差(EM)以及细胞内钾、钠活性((K)i、(Na)i)或细胞内和管腔pH值。
1)db-cAMP使EM超极化8.0 mV,同时(K)i增加4.8 mEq/l;2)向肾小管周围给予高钾(13.5和50 mM)溶液分别使EM去极化11.5和41.5 mV。含db-cAMP的高钾灌注液产生的去极化程度与不含db-cAMP的单纯高钾灌注相同;3)db-cAMP短暂阻断管腔酸化,同时细胞碱化约0.1 pH;4)db-cAMP使(Na)i降低5.0 mEq/l。
1)cAMP导致肾小管周围膜钾通透性增加;2)cAMP通过增强氢离子向亚细胞囊泡的掺入诱导细胞溶质碱中毒,从而有利于钠钾泵的激活;3)cAMP实际上抑制管腔膜中的钠氢交换机制并短暂阻断近端尿液酸化。