Loh Shih-Hurng, Lee Chung-Yi, Chen Gunng-Shinng, Wu Ching-Hsia, Tsao Chan-Jun, Shih Shou-Jou, Chou Chi-Chung, Tsai Chien-Sung, Tsai Yi-Ting
Department of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Department of Surgery, Division of Cardiovascular Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Alcohol Clin Exp Res. 2015 Dec;39(12):2302-12. doi: 10.1111/acer.12892. Epub 2015 Nov 18.
The presence of intracellular pH (pHi ) regulators, including Na(+) -H(+) exchanger (NHE), Na(+) -HCO3- co-transporter (NBC), Cl(-) /OH(-) exchanger (CHE), and Cl(-) /HCO3- exchanger (AE), have been confirmed in many mammalian cells. Alcohol consumption is associated with increased risk of cardiovascular disorder. The aims of the study were to identify the possible transmembrane pHi regulators and to explore the effects of ethanol (EtOH) (10 to 300 mM) on the resting pHi and pHi regulators in human aorta smooth muscle cells (HASMCs).
HASMCs were obtained from patients undergoing heart transplant. The pHi was measured by microspectrofluorimetry with the pH-sensitive dye, BCECF-AM.
The following results are obtained. (i) In cultured HASMCs, the resting pHi was 7.19 ± 0.04 and 7.13 ± 0.02 for HEPES- and CO2 /HCO3--buffered solution, respectively. (ii) Two different Na(+) -dependent acid-equivalent extruders, including NHE and Na(+) -coupled HCO3- transporter, functionally coexisted. (iii) Two different Cl(-) -dependent acid loaders (CHE and AE) were functionally identified. (iv) EtOH induced a biphasic, concentration-dependent change in resting pHi (+0.25 pH unit at 100 mM but only +0.05 pH unit at 300 mM) in bicarbonate-buffered solution, while caused a concentration-dependent decrease in resting pHi (-0.06 pH unit at 300 mM) in HEPES-buffered solution. (v) The effect of EtOH on NHE activity was also biphasic: increase of 40% at lower concentration of 10 mM, followed by decrease of 30% at higher concentration of 300 mM. (vi) The increase in Na(+) -coupled HCO3- transporter activity by EtOH was concentration dependent. (vii) The effect of EtOH on CHE and AE activities was both biphasic: increase of ~25% at 30 mM, followed by decrease of 10 to 25% at 100 mM, and finally increase of 15 to 20% at 300 mM.
This study demonstrated that 2 acid extruders and 2 acid loaders coexisted functionally in HASMCs and that EtOH induced a biphasic, concentration-dependent change in resting pHi by altering the activity of the 2 acid extruders, NHE and Na(+) -coupled HCO3- transporter, and the 2 acid loaders, CHE and AE.
细胞内pH(pHi)调节因子的存在,包括钠氢交换体(NHE)、钠-碳酸氢根协同转运体(NBC)、氯/氢氧根交换体(CHE)和氯/碳酸氢根交换体(AE),已在许多哺乳动物细胞中得到证实。饮酒与心血管心血管心血管疾病风险增加有关。本研究的目的是确定可能的跨膜pHi调节因子,并探讨乙醇(EtOH)(10至300 mM)对人主动脉平滑肌细胞(HASMCs)静息pHi和pHi调节因子的影响。
HASMCs取自接受心脏移植的患者。使用pH敏感染料BCECF-AM通过显微荧光分光光度法测量pHi。
获得了以下结果。(i)在培养的HASMCs中,对于HEPES缓冲溶液和CO2/HCO3-缓冲溶液,静息pHi分别为7.19±0.04和7.13±0.02。(ii)两种不同的钠依赖性酸当量排出器,包括NHE和钠偶联的HCO3-转运体,在功能上共存。(iii)在功能上鉴定出两种不同的氯依赖性酸加载器(CHE和AE)。(iv)在碳酸氢盐缓冲溶液中,EtOH诱导静息pHi出现双相、浓度依赖性变化(100 mM时为+0.25 pH单位,但300 mM时仅为+0.05 pH单位),而在HEPES缓冲溶液中导致静息pHi浓度依赖性降低(300 mM时为-0.06 pH单位)。(v)EtOH对NHE活性的影响也是双相的:在较低浓度10 mM时增加40%,随后在较高浓度300 mM时降低30%。(vi)EtOH对钠偶联的HCO3-转运体活性的增加是浓度依赖性的。(vii)EtOH对CHE和AE活性的影响都是双相的:在30 mM时增加约25%,随后在100 mM时降低10%至25%,最后在300 mM时增加15%至20%。
本研究表明,两种酸排出器和两种酸加载器在HASMCs中功能上共存,并且EtOH通过改变两种酸排出器NHE和钠偶联的HCO3-转运体以及两种酸加载器CHE和AE的活性,诱导静息pHi出现双相、浓度依赖性变化。