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
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.