ATP and [3H]noradrenaline release and the presence of ecto-Ca(2+)-ATPases in the capsule-glomerulosa fraction of the rat adrenal gland

J Endocrinol. 1997 Apr;153(1):105-14. doi: 10.1677/joe.0.1530105.

Abstract

Both [3H]noradrenaline ([3H]NA) and ATP were released in response to supramaximal electric field stimulation in superfused rat adrenal capsule-glomerulosa preparations. The voltage-dependent potassium channel blocker 4-aminopyridine enhanced, while the ATP-sensitive potassium channel blocker glibenclamide failed to affect the stimulation-evoked release of [3H]NA. The selective alpha 2-adrenoceptor antagonist CH-38083 enhanced the evoked release of [3H]NA while the P2 receptor agonist ATP and alpha, beta-methylene-ATP failed to affect it. Neither the adenosine A1 receptor agonist N6-cyclopentyl-adenosine (CPA) nor the adenosine A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX) influenced the stimulation-evoked [3H]NA release. The data showed that ATP was released from capsule-glomerulosa preparations in response to field stimulation together with but independently from [3H]NA, and that the local noradrenergic varicose axon terminals are not equipped with purinoceptors sensitive to ATP and/or adenosine. High concentrations of ATP also stimulated steroid hormone secretion in vitro, and thus may have a physiological role in this tissue. The presence of ecto-Ca(2+)-ATPases, enzymes able to terminate the effect of ATP, was demonstrated around the nerve profiles at the border of the capsule and zona glomerulosa tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Aminopyridine / pharmacology
  • Adenosine Triphosphate / metabolism*
  • Adenosine Triphosphate / pharmacology
  • Adrenal Glands / drug effects
  • Adrenal Glands / metabolism
  • Adrenal Glands / physiology*
  • Adrenergic alpha-Antagonists / pharmacology
  • Animals
  • Berberine / analogs & derivatives
  • Berberine / pharmacology
  • Calcium-Transporting ATPases / analysis
  • Calcium-Transporting ATPases / metabolism*
  • Electric Stimulation*
  • Glyburide / pharmacology
  • Histocytochemistry
  • Male
  • Microscopy, Electron
  • Norepinephrine / metabolism*
  • Organ Culture Techniques
  • Potassium Channel Blockers
  • Rats
  • Rats, Wistar
  • Tetrodotoxin / pharmacology
  • Tritium

Substances

  • Adrenergic alpha-Antagonists
  • Potassium Channel Blockers
  • Berberine
  • Tritium
  • 7,8-(methylenedioxy)-14-hydroxyberbane
  • Tetrodotoxin
  • Adenosine Triphosphate
  • 4-Aminopyridine
  • Calcium-Transporting ATPases
  • Glyburide
  • Norepinephrine