Gao Jun, Wu Long-Jun, Xu Lin, Xu Tian-Le
School of Life Sciences, University of Science and Technology of China, Hefei.
Brain Res. 2004 Aug 13;1017(1-2):197-207. doi: 10.1016/j.brainres.2004.05.046.
The characterization of acid-sensing ion channel (ASIC)-like currents has been reported in hippocampal neurons in primary culture. However, it is suggested that the profile of expression of ASICs changes in culture. In this study, we investigated the properties of proton-activated current and its modulation by extracellular Ca(2+) and Zn(2+) in neurons acutely dissociated from the rat hippocampal CA1 using conventional whole-cell patch-clamp recording. A rapidly decaying inward current and membrane depolarization was induced by exogenous application of acidic solution. The current was sensitive to the extracellular proton with a response threshold of pH 7.0-6.8 and the pH(50) of 6.1, the reversal potential close to the Na(+) equilibrium potential. It had a characteristic of acid-sensing ion channels (ASICs) as demonstrated by its sensitivity to amiloride (IC(50)=19.6+/-2.1 microM). Either low Ca(2+) or high Zn(2+) increased the amplitude of the current. All these characteristics are consistent with a current mediated through a mixture of homomeric ASIC1a and heteromeric ASIC1a+2a channels and closely replicate many of the characteristics that have been previously reported for hippocampal neurons cultured for a week or more, indicating that culture artifacts do not necessarily flaw the properties of ASICs. Interestingly, we found that high Zn(2+) (>10(-4) M) slowed the decay time constant of the ASIC-like current significantly in both acutely dissociated and cultured hippocampal neurons. In addition, the facilitating effects of low Ca(2+) and high Zn(2+) on the ASIC-like current were not additive. Since tissue acidosis, extracellular Zn(2+) elevation and/or Ca(2+) reduction occur concurrently under some physiological and/or pathological conditions, the present observations suggest that hippocampal ASICs may offer a novel pharmacological target for therapeutic invention.
在原代培养的海马神经元中已报道了酸敏感离子通道(ASIC)样电流的特征。然而,有人提出ASICs的表达谱在培养过程中会发生变化。在本研究中,我们使用传统的全细胞膜片钳记录技术,研究了从大鼠海马CA1区急性分离的神经元中质子激活电流的特性及其受细胞外Ca(2+)和Zn(2+)的调节。外源施加酸性溶液可诱导出快速衰减的内向电流和膜去极化。该电流对细胞外质子敏感,响应阈值为pH 7.0 - 6.8,pH(50)为6.1,反转电位接近Na(+)平衡电位。它具有酸敏感离子通道(ASICs)的特征,对氨氯吡咪敏感(IC(50)=19.6±2.1 microM)。低Ca(2+)或高Zn(2+)均可增加电流幅度。所有这些特征与通过同聚ASIC1a和异聚ASIC1a + 2a通道混合物介导的电流一致,并紧密复制了先前报道的培养一周或更长时间的海马神经元的许多特征,表明培养假象不一定会影响ASICs的特性。有趣的是,我们发现高Zn(2+)(>10(-4) M)在急性分离和培养的海马神经元中均显著减慢了ASIC样电流的衰减时间常数。此外,低Ca(2+)和高Zn(2+)对ASIC样电流的促进作用不是相加的。由于在某些生理和/或病理条件下会同时发生组织酸中毒、细胞外Zn(2+)升高和/或Ca(2+)降低,目前的观察结果表明海马ASICs可能为治疗干预提供一个新的药理学靶点。