Insulin Induces Cation Fluxes and Increases Intracellular Calcium in the HTC Rat Hepatoma Cell Line. (1st May 2000)

• Record Type: Journal Article
• Authors: Mathé, Laurence; Vallerand, Diane; Haddad, Pierre S
• Is Part Of: Canadian Journal of Gastroenterology. Volume 14:Number 5(2000)
• Page Start: 389
• Page End: 396
• Publication Date: 2000-05-01
• Subjects: Fura-2 -- Hepatocytes -- Nonselective cation channels -- Patch clamping
• DOI: 10.1155/2000/574820
• Languages: English
• ISSNs: 0835-7900

Abstract

Abstract : BACKGROUND/AIMS: Rat hepatoma HTC cells were used to study conductive pathways implicated in insulin-induced cation and calcium influx into liver cells. METHODS: Membrane potentials and currents were measured by whole-cell patch clamp. Cytosolic calcium was measured using FURA-2 fluorescence. RESULTS: Insulin induced a gradual and reversible depolarization of 5.7±0.8 mV. Insulin-induced currents showed a linear slope conductance of 663 pS and a reversal potential of -17.9 mV. Ion substitution experiments showed that these currents were composed mainly of a nonselective cation component. In FURA-2 experiments, insulin caused a slow monophasic rise in HTC cell calcium, which depended on the presence of extracellular calcium. Insulin also induced significant increases of 1.58- and 1.54-fold in basal calcium influx when studied by external calcium withdrawal and readmission, or by the manganese quench method, respectively. Using the latter approach, we found that 100 µM gadolinium and 10 µM SKF96365 blocked the rise of the basal manganese quench rate induced by insulin whereas 100 µM verapamil was without effect. CONCLUSIONS: Insulin induces inward cation currents that depolarize HTC cell membrane potentials and participate in increased calcium influx.