Electrogenic Na-Ca exchange has been known to act in the cardiac sarcolemma as a major mechanism for extruding Ca ions. Ionic flux measurements in cardiac vesicles have recently suggested that the exchange ratio is probably 3 Na:1 Ca, although a membrane current generated by such a process has not been isolated. Using the intracellular perfusion technique combined with the whole-cell voltage clamp, we were able to load Na+ inside and Ca2+ outside the single ventricular cells of the guinea pig and have succeeded in recording an outward Na-Ca exchange current while blocking most other membrane currents. The current is voltage-dependent, blocked by La3+ and does not develop in the absence of intracellular free Ca2+. This report presents the first direct measurement of the cardiac Na-Ca exchange current, and should facilitate the study of Ca2+ fluxes during cardiac activity, together with various electrical changes attributable to the Na-Ca exchange and the testing of proposed models.
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http://dx.doi.org/10.1038/319596a0 | DOI Listing |
RSC Adv
January 2025
Electronic Material Research Center, Northwest Institute for Nonferrous Metal Research Xi'an 710016 China.
Potassium is a harmful impurity in the rhenium sinter, which adversely affects its mechanical properties by significantly reducing the density of sintered rhenium. Cationic resin is a promising material for potassium removal. In this study, the strong acid cationic exchange resin C160H was pretreated with an HNO solution to enhance its performance in potassium removal.
View Article and Find Full Text PDFBiomed Pharmacother
January 2025
Department of Biology, University of Naples Federico II, Naples, Italy; Biogem, Istituto di Biologia e Genetica Molecolare, Ariano Irpino, AV, Italy.
Intracellular Ca homeostasis dysregulation, through the modulation of calcium permeable ion channels and transporters, is gaining attention in cancer research as an apoptosis evasion mechanism. Recently, we highlighted a prognostic role for several calcium permeable channels. Among them, here, we focused on the plasma membrane bidirectional Na/Ca exchanger SLC8A1.
View Article and Find Full Text PDFHuan Jing Ke Xue
January 2025
College of Hydraulic and Civil Engineering, Xinjiang Agricultural University, Urumqi 830052, China.
To explore the changes in groundwater hydrochemistry and its source influence in the low water level period of the southern oasis area of Gaochang District, Turpan City before and after the management of groundwater overexploitation, based on 12 groups of water samples in 2016 (three groups of unconfined water, nine groups of confined water) and 18 groups of water samples in 2023 (five groups of unconfined water, thirteen groups of confined water), mathematical statistics, hydrochemical diagraph, hydrogen and oxygen isotope means, and an absolute principle component-multiple linear regression (APCS-MLR) model were used to analyze the changes and sources of groundwater hydrochemistry. The results showed that due to the dynamic conditions of groundwater, the dominant cation changed from Na to Ca, and the anion changed from HCO to SO. The dominant cation of confined water changed from Ca to Na, and the dominant anion remained unchanged as SO.
View Article and Find Full Text PDFFront Physiol
December 2024
Physiological Laboratory, University of Cambridge, Cambridge, United Kingdom.
Introduction: Intracellular Ca signalling regulates membrane permeabilities, enzyme activity, and gene transcription amongst other functions. Large transmembrane Ca electrochemical gradients and low diffusibility between cell compartments potentially generate short-lived, localised, high-[Ca] microdomains. The highest concentration domains likely form between closely apposed membranes, as at amphibian skeletal muscle transverse tubule-sarcoplasmic reticular (T-SR, triad) junctions.
View Article and Find Full Text PDFCell Calcium
January 2025
Cardiac Signaling Center of USC, MUSC and Clemson University, 68 President St BEB 306, Charleston, SC 29425, USA. Electronic address:
Rationale & Methods: While signaling of cardiac SR by surface membrane proteins (I & I) is well studied, the regulation of mitochondrial Ca by plasmalemmal proteins remains less explored. Here we have examined the signaling of mitochondria and SR by surface-membrane calcium-transporting proteins, using genetically engineered targeted fluorescent probes, mito-GCamP6 and R-CEPIA1er.
Results: In voltage-clamped and TIRF-imaged cardiomyocytes, low Na induced SR Ca release was suppressed by short pre-exposures to ∼100 nM FCCP, suggesting mitochondrial Ca contribution to low Na triggered SR Carelease.
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