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首页> 外文期刊>Pfluegers Archiv: European Journal of Physiology >Electrophysiological evidence for an ATP-gated ion channel in the principal cells of the frog skin epithelium.
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Electrophysiological evidence for an ATP-gated ion channel in the principal cells of the frog skin epithelium.

机译:青蛙皮肤上皮细胞中ATP门控离子通道的电生理证据。

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In the present study we investigated the effects of adenosine 5'-triphosphate (ATP) on Na+ transport in frog skin epithelium. An experimental set-up was constructed to allow simultaneous measurement of Na+ transport, measured as the amiloride-sensitive short circuit current (Isc), and free cytosolic Ca2+ concentration ([Ca2+]i) measured with the Ca(2+)-sensitive dye fura-2. The cell potential (Vsc) was measured with microelectrodes. Addition of ATP (100 micrM) to the basolateral solution resulted in a fast transient decrease in Isc followed by a slower increase and a transient increase in [Ca2+]i. Microelectrode measurements showed that the primary response, i.e. the decline in Isc was accompanied by transient depolarisation, followed by a return to the control value. The decrease in current was Ca2+ independent; i.e. treatment with thapsigargin in Ca(2+)-free solutions abolished the Ca2+ transient but did not influence the current transient. The secondary response, i.e. the slow increase in current, was accompanied by slow depolarisation of the cell. Measurements of apical Na+ permeability showed that this was due to an opening or activation of apical Na+ channels. These data show that ATP causes a fast initial drop and a secondary, long-lasting increase in Na+ absorption. The ability of ATP to cause the initial decline in current is independent of Ca2+, i.e. it is not caused by secondary effects of the P2Y-type receptors present in the tissue. Measurements of intracellular potential indicate that the initial depolarisation is caused by opening of non-selective cation channels, suggesting that this decrease is due to a transient activation of P2X-type ATP receptors.
机译:在本研究中,我们研究了5'-三磷酸腺苷(ATP)对蛙皮上皮中Na +转运的影响。构建了一个实验装置,以允许同时测量Na +转运(以阿米洛利敏感的短路电流(Isc)进行测量)和以Ca(2+)敏感的染料测量的游离胞质Ca2 +浓度([Ca2 +] i)呋喃2。用微电极测量电池电位(Vsc)。在基底外侧溶液中添加ATP(100 micrM)会导致Isc的快速瞬时下降,然后[Ca2 +] i的上升缓慢且瞬时增加。微电极测量表明,主要反应,即Isc的下降伴随着瞬时去极化,随后返回到控制值。电流的减少与Ca2 +无关;即在无Ca(2+)的溶液中用毒胡萝卜素治疗可消除Ca2 +瞬变,但不影响电流瞬变。次要反应,即电流的缓慢增加,伴随着细胞的缓慢去极化。根尖Na +通透性的测量结果表明,这是由于根尖Na +通道的开放或激活所致。这些数据表明,ATP会引起Na +吸收的快速开始下降和持续的第二次持久增长。 ATP引起电流初始下降的能力与Ca2 +无关,也就是说,它不是由组织中存在的P2Y型受体的继发作用引起的。细胞内电位的测量表明,最初的去极化是由非选择性阳离子通道的开放引起的,表明这种下降是由于P2X型ATP受体的瞬时活化引起的。

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