Description:
<jats:p><jats:bold>Abstract: </jats:bold> Catecholamine (CA) secretion was evoked when the isolated rat adrenal gland was perfused with HEPES‐buffered Krebs solution acidified by the addition of HCI or by gassing with 95% O<jats:sub>2</jats:sub>/5% CO<jats:sub>2</jats:sub>. The secretion was detectable at pH 7.0 and increased with decreasing pH until at ∼6.4. The low pH‐induced CA secretion consisted of two phases, an initial transient response followed by a sustained phase. An intracellular Ca<jats:sup>2+</jats:sup> antagonist, 3,4,5‐trimethoxybenzoic acid 8‐(<jats:italic>N,N</jats:italic>‐diethylamino)octyl ester, selectively inhibited the initial phase of secretion. Both of the responses were resistant to nifedipine, a blocker of voltage‐gated Ca<jats:sup>2+</jats:sup> channel, but were completely inhibited in Ca<jats:sup>2+</jats:sup>‐free (1 m<jats:italic>M</jats:italic> EGTA containing) solution. Adrenaline was an exclusive component in CAs released by low pH. The time course and extent of intracellular acidification caused either by low pH in the external medium or by the offset of a transitory NH<jats:sub>4</jats:sub>CI application had no correlation with those of the secretory responses in the corresponding period. These results suggest that extracellular acidification preferentially activates adrenaline secretive cells to evoke CA secretion and that this low pH‐induced CA secretion may be mediated by dihydropyridine‐insensitive Ca<jats:sup>2+</jats:sup> influx. Furthermore, the initial transient phase of the low pH‐induced CA secretion might be caused by a Ca<jats:sup>2+</jats:sup> release from intracellular stores, which is also induced by the Ca<jats:sup>2+</jats:sup> influx.</jats:p>