Abstract
The central chemoreceptor neurons of the mammals were thought to be distributed over the ventral medullary surface (VMS) that is bathed in cerebrospinal fluid, and are stimulated by excess H+ to induce a hyperventilation. Using a voltage-sensitive dye, DiBAC4(3), we found the low dose of PCB (1 microM, Aroclor 1254) effects on the excitability of H+-sensitive neurons derived from the newborn rat VMS. In this study, we investigated that the effects of hydroxy PCB (4-OH-2',3,3',4',5'-pentachlorobiphenyl) on intracellular calcium concentrations ([Ca2+]i) in cultured neurons derived from the newborn rat VMS. To monitor [Ca2+]i in cultured neurons, we performed microfluorometric measurements using the fluorescent probe Fluo 3-AM. Expose of cultured neurons to hydroxy PCB dose-dependently increased [Ca2+]i . Cultured neurons exposed to 10, 50 and 100 nM hydroxy PCB showed increases in [Ca2+]i which were at exposure times of 10 min. Higher dose of hydroxy PCB (1 microM) reduced [Ca2+]i in the cultured neurons compared to elevations seen following exposure to 100 nM hydroxy PCB. The increase of [Ca2+]i in the hydroxy PCB solution was blocked with L-type Ca2+ channel blocker (10 microM nimodipine). These results suggest that the low dose of hydroxy PCB increases [Ca2+]i in cultured VMS neurons via a mechanism through L-type Ca2+ channels. [Jpn J Physiol 54 Suppl:S241 (2004)]