Project/Area Number |
14570035
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General physiology
|
Research Institution | Hirosaki University |
Principal Investigator |
TAKEO Teruko Hirosaki University School of Medicine, Associate Professor, 医学部, 助教授 (20113813)
|
Co-Investigator(Kenkyū-buntansha) |
WAKUI Makoto Hirosaki University School of Medicine, Professor, 医学部, 教授 (80108505)
|
Project Period (FY) |
2002 – 2003
|
Project Status |
Completed (Fiscal Year 2003)
|
Budget Amount *help |
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 2003: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 2002: ¥1,100,000 (Direct Cost: ¥1,100,000)
|
Keywords | hydrogen-peroxide / hepatocyte / calcium dynamics / phospholipase C / intracellular ATP / nonselective cation channel / Ca^<2+>homeostasis / oxygen radical / InsP_3 / Ca^<2+>oscillation / intracellular ATP / nonselective cation channel |
Research Abstract |
Development of ischemic-reperfusion injury is a major risk factor of liver transplantation. One of the mechanisms by which ischemic-reperfusion injury occurs is oxidative stress to liver cells (hepatocytes), occurring when pro-oxidants overwhelm cellular antioxidant defense mechanisms. In this oxidation process, an increase in intracellular Ca^<2+> concentration ([Ca^<2+>]i) is known to facilitate progression of cellular damage. In the present study, we investigated the effect of hydrogen peroxide (H_2O_2) on the Ca^<2+> dynamics of freshly isolated rat hepatocytes. And the following results were obtained. 1.H_2O_2 increased the level of [Ca^<2+>]_i of hepatocytes by mediating Ca^<2+> entry from extracellular fluid. 2.The membrane conductance of the hepatocytes was not acutely changed by H_2O_2 application. However, after several minutes exposure to H_2O_2, it gradually increased. 3.A removal of intracellular ATP by using a pipette solution with null ATP increased the membrane conductance via nonselective cation channels. 4.H_2O_2 reduced the ATP content in hepatocytes. 5.H_2O_2 augmented Ca^<2+> oscillations induced by phenylephrine through α_1-adrenoceptors, and 2APB inhibited both the phenylephrine and H_2O_2 effects. 6.H_2O_2 increased the activity of phospholipase C (PLC). 7.Amiloride (nonselective cation channel inhibitor) and U73122 (PLC inhibitor) prevented the H_2O_2-induced elevation of [Ca^<2+>]i. These results suggest that in rat hepatocytes, H_2O_2 induced intracellular Ca^<2+> mobilization, which was closely related with PLC activity and nonselective cation channels. At present, we have no evidence to support or refute the possibility that H_2O_2 affects plasma membrane Ca^<2+> pump or Ca^<2+>/Na^+ exchange system.
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