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10.1016/0005-2736(93)90023-s

http://scihub22266oqcxt.onion/10.1016/0005-2736(93)90023-s
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8391320!ä!8391320

suck abstract from ncbi


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pmid8391320      Biochim+Biophys+Acta 1993 ; 1149 (1): 49-54
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  • Na(+)- and anion-dependent Mg2+ influx in isolated hepatocytes #MMPMID8391320
  • Gunther T; Hollriegl V
  • Biochim Biophys Acta 1993[Jun]; 1149 (1): 49-54 PMID8391320show ga
  • Hepatocytes, which were Mg(2+)-depleted during isolation, took up Mg2+ during reincubation. Mg2+ uptake was dependent on the concentration of extracellular Mg2+, Na+, Cl-, bicarbonate and phosphate. Li+ and choline+ did not substitute for extracellular Na+ in Mg2+ influx. Mg2+ influx was maximal when all three anion species were present, and did not occur when these anions were replaced by gluconate. Bicarbonate, phosphate and Cl- could substitute for each other. Mg2+ uptake in hepatocytes was inhibited by p-chloromercuribenzene sulfonate, ouabain, gramicidin D, amiloride and verapamil. The results were explained by the assumption that net Mg2+ influx in hepatocytes is operating via electroneutral Na+, Mg2+/anion cotransport driven by the Na+ gradient. However, electrogenic Mg2+ uptake gated by extracellular Na+ and anions could not be excluded.
  • |4-Chloromercuribenzenesulfonate/pharmacology[MESH]
  • |Adenosine Triphosphate/metabolism[MESH]
  • |Animals[MESH]
  • |Bicarbonates/pharmacology[MESH]
  • |Biological Transport/drug effects[MESH]
  • |Chlorides/pharmacology[MESH]
  • |In Vitro Techniques[MESH]
  • |Liver/drug effects/*metabolism[MESH]
  • |Magnesium/*metabolism/pharmacology[MESH]
  • |Perfusion[MESH]
  • |Phosphates/pharmacology[MESH]
  • |Rats[MESH]


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