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首页> 外文期刊>The Journal of general physiology >Intracellular pH and Na fluxes in barnacle muscle with evidence for reversal of the ionic mechanism of intracellular pH regulation.
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Intracellular pH and Na fluxes in barnacle muscle with evidence for reversal of the ionic mechanism of intracellular pH regulation.

机译:藤壶肌细胞内pH和Na通量具有逆转细胞内pH调节离子机制的证据。

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The ion transport mechanism that regulates intracellular pH (pHi) in giant barnacle muscle fibers was studied by measuring pHi and unidirectional Na+ fluxes in internally dialyzed fibers. The overall process normally results in a net acid extrusion from the cell, presumably by a membrane transport mechanism that exchanges external Na+ and HCO-3 for internal Cl- and possibly H+. However, we found that net transport can be reversed either by lowering [HCO-3]o and pHo or by reducing [Na+]o. This reversal (acid uptake) required external Cl-, was stimulated by raising [Na+]i, and was blocked by SITS. When the transporter was operating in the net forward direction (acid extrusion), we found a unidirectional Na+ influx of approximately 60 pmol . cm-2 . s-1, which required external HCO-3 and internal Cl- and was stimulated by cyclic AMP and blocked by SITS or DIDS. These properties of the Na+ influx are all shared with the net acid extrusion process. We also found that under conditions of net forward transport, the pHi-regulating system mediated a unidirectional Na+ efflux, which was significantly smaller than the simultaneous Na+ influx. These data are consistent with a reversible transport mechanism which, even when operating in the net forward direction, mediates a small amount of reversed transport. We also found that the ouabain-sensitive Na+ efflux was sharply inhibited by acidic pHi, being totally absent at pHi values below approximately 6.8.
机译:通过测量内部透析纤维中的pHi和单向Na +通量,研究了调节巨型藤壶肌纤维中细胞内pH(pHi)的离子转运机制。整个过程通常会导致细胞产生净酸,大概是通过膜转运机制将外部Na +和HCO-3交换为内部Cl-以及可能的H +。但是,我们发现可以通过降低[HCO-3] o和pHo或降低[Na +] o来逆转净运输。这种逆转(酸吸收)需要外部Cl-,通过提高[Na +] i来刺激,并被SITS阻止。当转运蛋白在净正向运行(酸挤出)时,我们发现单向Na +流入量约为60 pmol。厘米2。 s-1,其需要外部HCO-3和内部Cl-,并受到环状AMP的刺激,并被SITS或DIDS阻断。 Na +流入的这些特性在净酸挤出过程中都具有。我们还发现,在净向前运输的条件下,pHi调节系统介导了单向Na +流出,其显着小于同时发生的Na +流入。这些数据与可逆传输机制一致,该机制即使在净正向运行时也可介导少量反向传输。我们还发现,酸性pHi强烈抑制了哇巴因对Na +的流出,在pHi值低于约6.8时完全不存在。

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