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10.1074/jbc.M008101200

http://scihub22266oqcxt.onion/10.1074/jbc.M008101200
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11278387!ä!11278387

suck abstract from ncbi


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pmid11278387      J+Biol+Chem 2001 ; 276 (17): 13657-63
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  • Angiotensin II type I receptor modulates intracellular free Mg2+ in renally derived cells via Na+-dependent Ca2+-independent mechanisms #MMPMID11278387
  • Touyz RM; Mercure C; Reudelhuber TL
  • J Biol Chem 2001[Apr]; 276 (17): 13657-63 PMID11278387show ga
  • Treatment of Madin-Darby canine kidney (MDCK) cells with the peptide hormone angiotensin II (Ang II) results in an increase in the concentrations of cytosolic free calcium ([Ca(2+)](i)) and sodium ([Na(+)](i)) with a concomitant decrease in cytosolic free Mg(2+) concentration ([Mg(2+)](i)). In the present study we demonstrate that this hormone-induced decrease in [Mg(2+)](i) is independent of [Ca(2+)](i) but dependent on extracellular Na(+). [Mg(2+)](i), [Ca(2+)](i), and [Na(+)](i) were measured in Ang II-stimulated MDCK cells by fluorescence digital imaging using the selective fluoroprobes mag-fura-2AM, fura-2AM, and sodium-binding benzofuran isophthalate (acetoxymethyl ester), respectively. Ang II decreased [Mg(2+)](i) and increased [Na(+)](i) in a dose-dependent manner. These effects were inhibited by irbesartan (selective AT(1) receptor blocker) but not by PD123319 (selective AT(2) receptor blocker). Imipramine and quinidine (putative inhibitors of the Na(+)/Mg(2+) exchanger) and removal of extracellular Na(+) abrogated Ang II-mediated [Mg(2+)](i) effects. In cells pretreated with thapsigargin (reticular Ca(2+)-ATPase inhibitor), Ang II-stimulated [Ca(2+)](i) transients were attenuated (p < 0.01), whereas agonist-induced [Mg(2+)](i) responses were unchanged. Clamping the [Ca(2+)](i) near 50 nmol/liter with 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) inhibited Ang II-induced [Ca(2+)](i) increases but failed to alter Ang II-induced [Mg(2+)](i) responses. Benzamil, a selective blocker of the Na(+)/Ca(2+) exchanger, inhibited [Na(+)](i) but not [Mg(2+)](i) responses. Our data demonstrate that in MDCK cells, AT(1) receptors modulate [Mg(2+)](i) via a Na(+)-dependent Mg(2+) transporter that is not directly related to [Ca(2+)](i). These data support the notion that rapid modulation of [Mg(2+)](i) is not simply a result of Mg(2+) redistribution from intracellular buffering sites by Ca(2+) and provide evidence for the existence of a Na(+)-dependent, hormonally regulated transporter for Mg(2+) in renally derived cells.
  • |3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester/pharmacology[MESH]
  • |Adrenergic Uptake Inhibitors/pharmacology[MESH]
  • |Adrenergic alpha-Antagonists/pharmacology[MESH]
  • |Amiloride/analogs & derivatives/pharmacology[MESH]
  • |Angiotensin II/pharmacology[MESH]
  • |Animals[MESH]
  • |Antihypertensive Agents/pharmacology[MESH]
  • |Benzofurans/pharmacology[MESH]
  • |Biphenyl Compounds/pharmacology[MESH]
  • |Calcium Channel Agonists/pharmacology[MESH]
  • |Calcium/*metabolism[MESH]
  • |Cell Line[MESH]
  • |Cells, Cultured[MESH]
  • |Chelating Agents/pharmacology[MESH]
  • |Cytosol/metabolism[MESH]
  • |Dogs[MESH]
  • |Dose-Response Relationship, Drug[MESH]
  • |Egtazic Acid/analogs & derivatives/pharmacology[MESH]
  • |Ethers, Cyclic/pharmacology[MESH]
  • |Fluorescent Dyes/pharmacology[MESH]
  • |Fura-2/*analogs & derivatives/pharmacology[MESH]
  • |Imidazoles/pharmacology[MESH]
  • |Imipramine/pharmacology[MESH]
  • |Irbesartan[MESH]
  • |Kidney/*metabolism[MESH]
  • |Kinetics[MESH]
  • |Magnesium/*metabolism[MESH]
  • |Microscopy, Fluorescence[MESH]
  • |Peptides/pharmacology[MESH]
  • |Pyridines/pharmacology[MESH]
  • |Quinidine/pharmacology[MESH]
  • |Receptor, Angiotensin, Type 1[MESH]
  • |Receptor, Angiotensin, Type 2[MESH]
  • |Receptors, Angiotensin/*physiology[MESH]
  • |Sodium/*metabolism/pharmacology[MESH]
  • |Tetrazoles/pharmacology[MESH]


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