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To analyze vasopressin-induced Ca 2+ increase in liver cells, rat hepatocytes were isolated and attached to collagen-coated cover slips. Usipg fura-2, a Ca 2+ -sensing dye, changes in intracellular Ca 2+ concentration by vasopressin were monitored. Results in this communication suggested that vasopressin-induced Ca 2+ increase were composed of both Ca 2+ release from internal Ca 2+ stores and influx from the plasma membrane. The Ca 2+ influx consisted of two distinguishable components. One was dependent on the presence of vasopressin and the other was not. SK&F96365 blocked vasopressin-induced Ca 2+ influx in a dose-dependent manner. Vasopressin-induced Ca 2+ release from internal stores diminished in a primary culture of hepatocytes according to the culture time. However, changes in vasopressin-induced Ca 2+ influx across the plasma membrane differed from changes in the Ca 2+ release from internal stores, suggesting two separate signalings from receptor activation to internal stores and to the plasma membrane.
Archives of Pharmacal Research – Springer Journals
Published: Jan 1, 2003
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