Kiechle F L, Bailey F, Hill N, Malinski T
Department of Clinical Pathology, William Beaumont Hospital, Royal Oak, MI 48073-6769.
Ann Clin Lab Sci. 1994 Mar-Apr;24(2):164-72.
The change in transmembrane potential of rat adipocytes was measured using the fluorescent probe 3,3'-diethylthiadicarbocyanine iodide, diS-C2-(5). The method was calibrated by altering the potassium ion concentration while keeping the sum of potassium and sodium ions at a constant concentration of 153 mM (Bailey et al: Bioelectrochem. Bioenergetics 21:333-42, 1989). Two insulin-mimetic agents, phospholipase C from Clostridium perfringens and concanavalin A, induced a dose dependent hyperpolarization of rat epididymal adipocytes, like insulin. Removal of endogenous adenosine with adenosine deaminase or adenosine receptor blockade with isobutylmethylxanthine following the initiation of insulin-induced hyperpolarization resulted in depolarization. These same agents induced hyperpolarization of -6 to -8 mV when added without insulin. The replacement of adenosine with its analogue, N6-phenylisopropyladenosine, plus insulin depolarized the cells toward the transmembrane potential established by insulin, -2.0 mV. These studies suggest that adenosine receptor occupancy is required to maintain insulin-induced hyperpolarization.
使用荧光探针3,3'-二乙基硫代二羰花青碘化物(diS-C2-(5))测量大鼠脂肪细胞跨膜电位的变化。通过改变钾离子浓度同时保持钾离子和钠离子的总和在153 mM的恒定浓度下对该方法进行校准(贝利等人:《生物电化学与生物能量学》21:333 - 42,1989)。两种胰岛素模拟剂,产气荚膜梭菌的磷脂酶C和伴刀豆球蛋白A,像胰岛素一样诱导大鼠附睾脂肪细胞产生剂量依赖性超极化。在胰岛素诱导的超极化开始后,用腺苷脱氨酶去除内源性腺苷或用异丁基甲基黄嘌呤阻断腺苷受体导致去极化。当在没有胰岛素的情况下添加这些相同的试剂时,它们会诱导 -6至 -8 mV的超极化。用其类似物N6-苯基异丙基腺苷替代腺苷并加入胰岛素会使细胞朝着胰岛素建立的跨膜电位 -2.0 mV去极化。这些研究表明,需要占据腺苷受体来维持胰岛素诱导的超极化。