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10.1152/ajpgi.2000.279.5.G943

http://scihub22266oqcxt.onion/10.1152/ajpgi.2000.279.5.G943
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11052991!ä!11052991

suck abstract from ncbi


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pmid11052991      Am+J+Physiol+Gastrointest+Liver+Physiol 2000 ; 279 (5): G943-50
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  • Activation of Na(+)- and Ca(2+)-dependent Mg(2+) extrusion by alpha(1)- and beta-adrenergic agonists in rat liver cells #MMPMID11052991
  • Fagan TE; Romani A
  • Am J Physiol Gastrointest Liver Physiol 2000[Nov]; 279 (5): G943-50 PMID11052991show ga
  • The administration of selective alpha(1) (phenylephrine)-, beta (isoproterenol)-, or mixed (epinephrine) adrenergic agonists induces a marked Mg(2+) extrusion from perfused rat livers. In the absence of extracellular Ca(2+), phenylephrine does not induce a detectable Mg(2+) extrusion, isoproterenol-induced Mg(2+) mobilization is unaffected, and epinephrine induces a net Mg(2+) extrusion that is lower than in the presence of extracellular Ca(2+) and quantitatively similar to that elicited by isoproterenol. In the absence of extracellular Na(+), no Mg(2+) is extruded from the liver irrespective of the agonist used. Similar results are observed in perfused livers stimulated by glucagon or 8-chloroadenosine 3', 5'-cyclic monophosphate. In the absence of extracellular Na(+) or Ca(2+), adrenergic-induced glucose extrusion from the liver is also markedly decreased. Together, these results indicate that liver cells extrude Mg(2+) primarily via a Na(+)-dependent mechanism. This extrusion pathway can be activated by the increase in cellular cAMP that follows the stimulation by glucagon or a specific beta-adrenergic receptor agonist or, alternatively, by the changes in cellular Ca(2+) induced by the stimulation of the alpha(1)-adrenoceptor. In addition, the stimulation of the alpha(1)-adrenoceptor appears to activate an auxiliary Ca(2+)-dependent Mg(2+) extrusion pathway. Finally, our data suggest that experimental conditions that affect Mg(2+) mobilization also interfere with glucose extrusion from liver cells.
  • |8-Bromo Cyclic Adenosine Monophosphate/*analogs & derivatives/pharmacology[MESH]
  • |Adrenergic Agonists/pharmacology[MESH]
  • |Adrenergic Uptake Inhibitors/pharmacology[MESH]
  • |Adrenergic alpha-Agonists/pharmacology[MESH]
  • |Adrenergic beta-Agonists/pharmacology[MESH]
  • |Amiloride/pharmacology[MESH]
  • |Animals[MESH]
  • |Calcium/*pharmacology[MESH]
  • |Diuretics/pharmacology[MESH]
  • |Epinephrine/pharmacology[MESH]
  • |Glucagon/pharmacology[MESH]
  • |Glucose/metabolism[MESH]
  • |Hepatocytes/chemistry/drug effects/*metabolism[MESH]
  • |Imipramine/pharmacology[MESH]
  • |Isoproterenol/pharmacology[MESH]
  • |Liver/cytology/metabolism[MESH]
  • |Magnesium/*metabolism[MESH]
  • |Male[MESH]
  • |Phenylephrine/pharmacology[MESH]
  • |Phloretin/pharmacology[MESH]
  • |Rats[MESH]
  • |Rats, Sprague-Dawley[MESH]
  • |Receptors, Adrenergic, alpha-1/*metabolism[MESH]
  • |Receptors, Adrenergic, beta/*metabolism[MESH]
  • |Sodium/*pharmacology[MESH]


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