THE EFFECT OF BARIUM ON [H-3] NORADRENALINE RELEASE FROM THE HUMAN NEUROBLASTOMA SH-SY5Y

Citation
Pft. Vaughan et al., THE EFFECT OF BARIUM ON [H-3] NORADRENALINE RELEASE FROM THE HUMAN NEUROBLASTOMA SH-SY5Y, European journal of neuroscience, 7(5), 1995, pp. 875-880
Citations number
40
Categorie Soggetti
Neurosciences
ISSN journal
0953816X
Volume
7
Issue
5
Year of publication
1995
Pages
875 - 880
Database
ISI
SICI code
0953-816X(1995)7:5<875:TEOBO[>2.0.ZU;2-F
Abstract
Replacement of Ca2+ with Ba2+ in HEPES-buffered saline stimulated [H-3 ]noradrenalin release in the human neuroblastoma clone SH-SY5Y by up t o 20% of the cell content in the absence of other secretory stimuli. T he Ba2+-evoked release was inhibited by 85% by 3 mu M tetrodotoxin and 95% by 5 mu M nifedipine. Ba2+ also increased the potency of K+-evoke d release of [H-3]noradrenalin, as maximal release was observed with 6 0 mM K+ compared with the 100 mM K+ necessary to achieve maximal relea se in the presence of Ca2+. In contrast, replacing Ca2+ with Ba2+ had little effect on carbachol- and bradykinin-evoked release of [H-3]nora drenalin. No evidence was obtained from studies on changes in [Ca2+](i ) ( in response to 100 mu M carbachol) using fura-2 that Ba2+ could en ter intracellular stores in SH-SY5Y cells. Whole-cell patch-clamp stud ies showed that Ba2+ depolarizes SH-SY5Y cells as well as enhancing in ward Ca2+ channel currents and shifting their voltage dependence to mo re negative values. These results are discussed in terms of the hypoth esis that Ba2+ blocks K+ channels, leading to depolarization followed by opening of voltage-sensitive Na+ channels. This in turn opens volta ge-sensitive L-type Ca2+ channels, which are coupled to the release of [H-3]noradrenalin in SH-SY5Y cells.