Sugiyama S, Satoh H, Nomura N, Terada H, Watanabe H, Hayashi H
Division of Cardiovascular Disease, Internal Medicine III, Hamamatsu University School of Medicine, Japan.
Mol Cell Biochem. 2001 Jan;217(1-2):153-61. doi: 10.1023/a:1007261322878.
The cardiac subtype of Na+/H+ exchanger (NHE-1) plays an important role in the regulation of intracellular pH (pHi) and also can be a major route for Na+ influx. Although intracellular ATP is required for the optimal function of NHE-1, the regulation of the exchanger by ATP is less well characterized. This study was designed to investigate which intracellular ATP generated by oxidative phosphorylation or by glycolysis is dominant for the activation of NHE-1 in intact cardiac myocytes. Isolated guinea pig ventricular myocytes were loaded with the pHi-sensitive fluorescent indicator, 2'-7'-bis(carboxyl)-5',6'-carboxy fluorescein (BCECF), and exposed to 20 mM 2-deoxyglucose (2-DG) or 2 mM sodium cyanide (CN) to inhibit glycolysis or oxidative phosphorylation, respectively. The activity of NHE-1 was estimated with pHi recovery following transient application of 15 mM NH4Cl (NH4Cl prepulse). After the NH4Cl prepulse, pHi decreased from 7.00 +/- 0.03 (mean +/- S.E.) to 6.60 +/- 0.06 and recovered to 6.94 +/- 0.13 at 10 min (n = 7). The pHi recovery was suppressed in the presence of 2-DG (6.67 +/- 0.05, p < 0.01, n = 7), but was not changed in the presence of CN (6.88 +/- 0.18, n = 6). Since there was no difference in the intrinsic H+ buffering power, the estimation of the net acid efflux demonstrated that the activity of NHE-1 was significantly depressed in 2-DG. The inhibitory effect of 2-DG was not due to more extensive depletion of global intracellular ATP or secondary to the change in either intracellular Na+ or Ca2+ concentration. We concluded that ATP generated by glycolysis rather than by oxidative phosphorylation is essential to activate NHE-1 in ventricular myocytes.
钠氢交换体(NHE-1)的心脏亚型在调节细胞内pH(pHi)方面发挥着重要作用,并且还可能是钠离子内流的主要途径。尽管细胞内ATP是NHE-1发挥最佳功能所必需的,但ATP对该交换体的调节作用尚未得到充分表征。本研究旨在探究通过氧化磷酸化或糖酵解产生的细胞内ATP中,哪一种对完整心肌细胞中NHE-1的激活起主导作用。分离的豚鼠心室肌细胞用pHi敏感的荧光指示剂2'-7'-双(羧基)-5',6'-羧基荧光素(BCECF)进行负载,并分别暴露于20 mM 2-脱氧葡萄糖(2-DG)或2 mM氰化钠(CN)以抑制糖酵解或氧化磷酸化。通过短暂施加15 mM氯化铵(NH4Cl预脉冲)后pHi的恢复来估计NHE-1的活性。在NH4Cl预脉冲后,pHi从7.00±0.03(平均值±标准误)降至6.60±0.06,并在10分钟时恢复至6.94±0.13(n = 7)。在2-DG存在的情况下,pHi的恢复受到抑制(6.67±0.05,p < 0.01,n = 7),但在CN存在的情况下未发生变化(6.88±0.18,n = 6)。由于内在的H+缓冲能力没有差异,净酸外排的估计表明NHE-1的活性在2-DG中显著降低。2-DG的抑制作用并非由于整体细胞内ATP的更广泛消耗,也不是细胞内Na+或Ca2+浓度变化的继发结果。我们得出结论,糖酵解产生的ATP而非氧化磷酸化产生的ATP对于激活心室肌细胞中的NHE-1至关重要。