N-methyl-D-aspartate induces a rapid, reversible, and calcium-dependent intracellular acidosis in cultured fetal rat hippocampal neurons

Abstract

The ability of NMDA to alter intracellular pH (pH(i)) was studied in fetal rat hippocampal neurons and glia using the pH-sensitive fluorescent indicator 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF). Brief exposure (60 sec) of hippocampal neurons to NMDA (2.5-250 μM) results in a rapid, and in most cells reversible, reduction in pH(i), with full recovery to baseline pH(i) values taking several minutes following removal of NMDA. In contrast, little or no change in pH(i) was observed in glial cells exposed to these same concentrations of NMDA. The NMDA-induced acidification of neurons was concentration and time dependent, with an EC50 of 39 μM and E(max) (ΔpH) of -0.53. More prolonged exposure to NMDA (≥ 10 min) resulted in a more prolonged reduction in pH(i) values over the ensuing 20 min observation period. The intracellular acidification resulting from NMDA exposure of hippocampal neurons was blocked by the NMDA receptor antagonist 3-((±)-2- carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP). Moreover, removal of extracellular Ca2+ eliminated both the selective NMDA-induced elevation in [Ca2+], and the reduction in pH(i), indicating that Ca2+ influx may be required for the decrease in pH(i) induced by NMDA receptor activation. Finally, the NMDA-induced reduction in pH(i) was not significantly attenuated when extracellular [H+] was decreased by increasing extracellular pH to 8.0. The latter suggests that an intracellular source of H+ is responsible for the NMDA-induced reduction in neuronal pH(i). The reduction in neuronal pH(i) induced by NMDA receptor activation may mediate some of the physiological and (or) pathophysiological actions of glutamate.