Wondergem R, Davis J
Department of Physiology, James H. Quillen College of Medicine, East Tennessee State University, Johnson City 37614-0576.
Alcohol Clin Exp Res. 1994 Oct;18(5):1230-6. doi: 10.1111/j.1530-0277.1994.tb00110.x.
Mouse hepatocytes respond to osmotic stress with adaptive changes in transmembrane potential, Vm, such that hypotonic stress hyperpolarizes cells and hypertonic stress depolarizes them. These changes in Vm provide electromotive force for redistribution of ions such as Cl-, and this comprises part of the mechanism of hepatocyte volume regulation. We conducted the present study to determine whether ethanol administered in vitro to mouse liver slices increases hepatocyte water volume, and whether this swelling triggers adaptive changes in the Vm. Cells in mouse liver slices were loaded with tetramethylammonium ion (TMA). Changes in hepatocyte water volume were computed from measurements with ion sensitive microelectrodes of changes in intracellular activity of TMA (a1TMA) that resulted from water fluxes. Ethanol (70 mM) increased hepatocyte water volume immediately, and this peaked at 17% by 7 to 8 min, by which time a plateau was reached. Liver slices also were obtained from mice treated 12 hr prior with 4-methylpyrazole (4 mM). The effect of ethanol on their hepatocyte water volume was identical to that from untreated mice, except that the onset and peak were delayed 2 min. Hepatocyte Vm showed no differences between control or ethanol-treated cells during the course of volume changes. In contrast, hyposmotic stress, created by dropping external osmolality 50 mosm, increased Vm from -30 mV to -46 mV. Ethanol did not inhibit this osmotic stress-induced hyperpolarization, except partially at high concentrations of 257 mM or greater. We infer that ethanol-induced swelling of hepatocytes differs from that resulting from hyposmotic stress.(ABSTRACT TRUNCATED AT 250 WORDS)
小鼠肝细胞通过跨膜电位(Vm)的适应性变化对渗透压应激作出反应,使得低渗应激使细胞超极化,高渗应激使细胞去极化。Vm的这些变化为诸如Cl-等离子的重新分布提供电动势,这构成了肝细胞体积调节机制的一部分。我们进行了本研究,以确定体外给予小鼠肝切片的乙醇是否会增加肝细胞水含量,以及这种肿胀是否会触发Vm的适应性变化。用四甲基铵离子(TMA)加载小鼠肝切片中的细胞。根据用离子敏感微电极测量由水通量引起的TMA细胞内活性(a1TMA)变化来计算肝细胞水含量的变化。乙醇(70 mM)立即增加肝细胞水含量,并在7至8分钟时达到17%的峰值,此时达到平台期。还从提前12小时用4-甲基吡唑(4 mM)处理的小鼠获得肝切片。乙醇对其肝细胞水含量的影响与未处理小鼠的相同,只是起始和峰值延迟了2分钟。在体积变化过程中,对照细胞或乙醇处理细胞之间的肝细胞Vm没有差异。相比之下,通过降低外部渗透压50 mosm产生的低渗应激使Vm从-30 mV增加到-46 mV。乙醇并不抑制这种渗透压应激诱导的超极化,除非在257 mM或更高的高浓度下有部分抑制。我们推断乙醇诱导的肝细胞肿胀与低渗应激引起的肿胀不同。(摘要截短于250字)