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10.1152/ajpendo.1990.258.4.E555

http://scihub22266oqcxt.onion/10.1152/ajpendo.1990.258.4.E555
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2333957!ä!2333957

suck abstract from ncbi


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pmid2333957      Am+J+Physiol 1990 ; 258 (4 Pt 1): E555-61
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  • Sustained stimulation of aldosterone production by angiotensin II is potentiated by nickel #MMPMID2333957
  • Spat A; Balla I; Balla T; Enyedi P; Hajnoczky G; Rohacs T
  • Am J Physiol 1990[Apr]; 258 (4 Pt 1): E555-61 PMID2333957show ga
  • Angiotensin-induced aldosterone production by superfused adrenal glomerulosa cells was potentiated by Ni2+ (0.1 mM), added either at the onset of stimulation with angiotensin II or 1 h later. Nickel did not influence the effect of adrenocorticotropic hormone or potassium on aldosterone production. Nickel failed to modify angiotensin-induced changes in phospholipid metabolism or the formation of inositol phosphates and slightly reduced the enhancement of 45Ca influx. Uptake of Ni2+ into glomerulosa cells was increased by depolarization in a dihydropyridine-insensitive manner. Because nickel selectively potentiates the sustained phase of the response to a calcium-mobilizing hormone, it may serve as a suitable tool in elucidating the signal transduction process during the sustained phase of stimulation.
  • |Aldosterone/*biosynthesis[MESH]
  • |Angiotensin II/*pharmacology[MESH]
  • |Animals[MESH]
  • |Biological Transport, Active/drug effects[MESH]
  • |Calcium/metabolism[MESH]
  • |Cobalt/pharmacology[MESH]
  • |Female[MESH]
  • |In Vitro Techniques[MESH]
  • |Inositol Phosphates/metabolism[MESH]
  • |Kinetics[MESH]
  • |Male[MESH]
  • |Nickel/metabolism/*pharmacology[MESH]
  • |Rats[MESH]
  • |Rats, Inbred Strains[MESH]


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