EFFECT OF INTRACELLULAR INJECTION OF INOSITOL TRISPHOSPHATE ON CYTOSOLIC CALCIUM AND MEMBRANE CURRENTS IN APLYSIA NEURONS

Pacemaker cells of Aplysia californica display a regular bursting that results from a complex interplay of Ca2+-mediated conductances and a continuous influx and extrusion of Ca2+. The effect of the second messenger 1,4,5-inositol trisphosphate (InsP3) on intracellular free Ca2+ concentration (Ca(i)) regulation and electrical properties was investigated in identified neurons of the abdominal ganglion (R15, L2-L4, L6). Double-barreled Ca-selective microelectrodes were used to pressure inject InsP3 and measure Ca(i) at the same point. Brief injection of InsP3 resulted in an average increase of Ca(i) of 9.2 +/- 10.0-mu-M (+/-SE; n = 14) that decayed in about 1 min. The InsP3-induced elevation of Ca(i) increased in a dose-dependent manner and saturated when large amounts of InsP3 were injected. The InsP3-induced Ca(i) increase was the result of mobilization from intracellular stores; Ca(i) could be repeatedly mobilized by InsP3 in cells superfused with 0 Ca artificial seawater for more than 60 min. Following multiple injections of InsP3, there was no evidence of immediate inhibition or facilitation. The spatial nature of the InsP3-induced Ca(i) increase was investigated by moving the double-barreled Ca-selective microelectrode tip in a stepwise manner relative to the membrane surface. The largest InsP3-induced Ca(i) increases were measured in an area 0-80-mu-m from the membrane surface; some cells had their largest InsP3-induced Ca(i) increase some 120-160-mu-m away from the membrane. Injection of InsP3 in a bursting neuron induced an immediate train of action potentials followed by membrane hyperpolarization and a decrease in the burst frequency. Injection of InsP3 in voltage-clamped cells induced a biphasic response: a rapid inward current followed by a more prolonged outward current; the temporal overlap of the currents was depth dependent. Injection of InsP3 or Ca2+ from a double-barreled injecting electrode induced currents that were different in waveform and time course, indicating that part of the conductance change induced by InsP3 is direct and not mediated by the mobilized Ca2+. In BAPTA [1,2-bis(2-aminophenoxy)ethane-NNN',N'tetra-acetic acid]-loaded cells, the InsP3-induced inward current was mostly unaffected while the Ca-induced outward current was largely attenuated. The results suggest that InsP3 mobilizes Ca2+ from discrete intracellular compartments and induces distinct changes in membrane currents that seem to be independent of the Ca(i) increase.