Cytosolic Calcium Alteration and Cell Injury by Silica in Rat Hepatocytes

  • Cha, Seok-Ho (Department of Biology, Chungnam National University) ;
  • Cha, Shin-Woo (Toxicology Research Center, Korea Research Institute of Chemical Technology) ;
  • Ko, Chang-Bo (Department of Biology, Chungnam National University) ;
  • Yu, Soung-Roung (Toxicology Research Center, Korea Research Institute of Chemical Technology) ;
  • Kim, Hye-Sun (Department of Pharmacology, College of Medicine, Seoul National University) ;
  • Paik, Sang-Gi (Department of Biology, Chungnam National Univers)
  • 발행 : 1998.12.01

초록

The purpose of this study was to clarify the effect of silica on cytosolic free calcium mobilization and cell injury in primary cultured rat hepatocytes. Cytosolic free calcium concentration ([Ca$^{2+}$]) was measured employing calcium sensitive fluorescent dye, Fura-2 / AM, and cell injury was evaluated by determination of cellular ATP contents. Silica increased [Ca$^{2+}$], in a concentration-dependent manner in hepatocytes (10$^{-5}$ ~10$^{-2}$ M). Silica caused a biphasic increase in [Ca$^{2+}$], which was composed of an initial rapid rise and following sustained phase. $Ca^{2+}$ removal from the medium resulted in abolishment of initial and sustained phase of silica (10$^{-2}$ M)-induced [Ca$^{2+}$], in hepatocytes. The pretreatment with nifedipine (1 $\mu$M) attenuated silica-induced [Ca$^{2+}$], increases. Silica decreased cellular ATP contents in a dose-dependent manner. This silica-induced cell injury was attenuated by the pretreatment with EGTA (100 $\mu$M) and nifedipine (1 $\mu$M). This study suggests that the elevation of [Ca$^{2+}$], caused by silica may be due mainly to influx through a plasma membrane $Ca^{2+}$ channel and hepatotoxicity by silica relate with alteration of calcium homeostasis.ium homeostasis.

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