The differential role of Na+/Ca2+ exchange in the regulation of intracellular ionized calcium ([Ca2+](i)) in immunological and pharmacologically identified type 1 astrocytes and Purkinje cells was studied in rat cerebellar culture, using Ca2+ (Fluo-3, Fura-2) and Na+ (SBFI) fluorescence measurements. The mean resting [Ca2+](i) was significantly higher (191 +/- 8 nm, n = 25) in type 1 astrocytes than in Purkinje cells (92 +/- 2.5 nm, n = 35). In contrast to Purkinje cells, in unstimulated cerebellar type 1 astrocytes, forward and reverse Na+/Ca2+ modes operate under resting physiological conditions, being responsible for most of the total Ca2+ transplasma membrane fluxes. Four observations support this hypothesis: (1) under resting conditions of temperature and ionic composition, Na-o(+) removal causes a remarkable increase in [Ca2+](i), being inhibited by 2', 4' dichlorobenzamil (DCB), and 2-[2-[4-(nitrobonzilloxiphenyl ethyl] isothiourea metanesulfonate (KB-R7943); (2) Ca-o(2+) removal in the presence of Na-o(+) causes an important drop in [Ca2+](i), which is absent in Li-o(+) or NMG(o)(+) (N-methyl-D-glucamine) containing medium; (3) the reverse mode exchange inhibitor KB-R7943 mimics the removal of Ca, only in the presence of Na-o(+); and (4) under loaded [Na+](i) conditions (ouabain or the activation of taurine-Na+-cotransport), reverse mode exchange increases in both astrocytes and Purkinje cells. In type 1 astrocytes stimulated with endothelin-3 (ET-3), the recovery of the Ca-i(2+) signal occurs largely through the Na+/Ca2+ exchanger. Genistein, a tyrosine kinase inhibitor, completely and reversibly blocks all exchange activity, but not its inactive analogue daidzein, thus suggesting that the Na+/Ca2+ exchanger of cerebellar type 1 astrocytes may be modulated by phosphorylation. Our main conclusion is that in rat cerebellar type 1 astrocytes under resting physiological conditions, most of the total transplasma membrane Ca2+ fluxes take place through the Na+/Ca2+ exchanger, thus accounting for the resting [Ca2+](i).