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小龙虾分隔轴突中缝隙连接电阻随酸化作用的增加与细胞内钙的变化密切相关,而与氢离子浓度的变化无关。

Increase in gap junction resistance with acidification in crayfish septate axons is closely related to changes in intracellular calcium but not hydrogen ion concentration.

作者信息

Peracchia C

机构信息

Department of Physiology, University of Rochester, New York.

出版信息

J Membr Biol. 1990 Jan;113(1):75-92. doi: 10.1007/BF01869608.

DOI:10.1007/BF01869608
PMID:2304073
Abstract

Neutral-carrier pH- and Ca-sensitive microelectrodes were used to investigate the relationship between junctional electrical resistance and either pHi or [Ca2+]i in crayfish septate axons uncoupled by acidification. For measuring [Ca2+]i a new neutral carrier sensor sensitive to picomolar [Ca2+] and virtually insensitive to other ions was used. Uncoupling was induced by superfusing the axons with Na-acetate solutions (pH 6.3). With acetate, the time course of changes in junctional resistance differed markedly from that of pHi or [H+]i, and [H+]i peaked 40-90 sec before junctional resistance. The difference in shape and peak time between pHi and junctional resistance curves caused significant hysteresis in the pHi versus junctional resistance relationship. In addition, junctional resistance maxima reached with slow acidification rates were 3-4 times greater than those with fast acidification of similar magnitude. With acetate, [Ca2+]i increased by approximately one order of magnitude from basal values of 0.1-0.3 microM. The curves describing the time course of changes in [Ca2+]i and junctional resistance matched well with each other in shape, peak time and magnitude. Both junctional resistance and [Ca2+]i recovered following a single exponential decay with a time constant of approximately 2 min. Different rates of acidification caused increases in [Ca2+]i and junctional resistance comparable in magnitude. The data indicate that the increase in junctional resistance induced by acidification is more closely related to [Ca2+]i than to [H+]i.

摘要

使用中性载体pH和钙敏感微电极,研究了在经酸化解偶联的小龙虾分隔轴突中,连接电阻与细胞内pH值(pHi)或细胞内钙离子浓度([Ca2+]i)之间的关系。为了测量[Ca2+]i,使用了一种对皮摩尔级[Ca2+]敏感且对其他离子几乎不敏感的新型中性载体传感器。通过用醋酸钠溶液(pH 6.3)灌注轴突来诱导解偶联。使用醋酸时,连接电阻变化的时间进程与pHi或细胞内氢离子浓度([H+]i)的变化时间进程明显不同,并且[H+]i在连接电阻之前40 - 90秒达到峰值。pHi与连接电阻曲线在形状和峰值时间上的差异导致了pHi与连接电阻关系中的显著滞后现象。此外,以缓慢酸化速率达到的连接电阻最大值比类似幅度的快速酸化时大3 - 4倍。使用醋酸时,[Ca2+]i从0.1 - 0.3微摩尔的基础值增加了大约一个数量级。描述[Ca2+]i和连接电阻变化时间进程的曲线在形状、峰值时间和幅度上相互匹配良好。连接电阻和[Ca2+]i在单次指数衰减后恢复,时间常数约为2分钟。不同的酸化速率导致[Ca2+]i和连接电阻的增加幅度相当。数据表明,酸化诱导的连接电阻增加与[Ca2+]i的关系比与[H+]i的关系更密切。

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