Analysis of inhibitory mechanism by ethanol on liver regeneration.
Project/Area Number |
62570323
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Research Category |
Grant-in-Aid for General Scientific Research (C)
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Allocation Type | Single-year Grants |
Research Field |
Gastroenterology
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Research Institution | Osaka University |
Principal Investigator |
FUSAMOTO Hideyuki Osaka University Medical School, Assistant, 医学部, 助手 (90124776)
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Co-Investigator(Kenkyū-buntansha) |
古澤 俊一 大阪大学, 医学部附属病院, 医員
SASAKI Yutaka Osaka University Hospital, Resident, 医学部附属病院, 医員 (70235282)
KASAHARA Akinori Osaka University Hospital, Resident, 医学部附属病院, 医員 (70214286)
FURUSAWA Shunichi Osaka University Hospital, Resident
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Project Period (FY) |
1987 – 1988
|
Project Status |
Completed (Fiscal Year 1988)
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Budget Amount *help |
¥2,500,000 (Direct Cost: ¥2,500,000)
Fiscal Year 1988: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1987: ¥1,300,000 (Direct Cost: ¥1,300,000)
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Keywords | liver regeneration / proto-oncogene / 肝再生 |
Research Abstract |
Expression of the proto-oncogenes such as c-fos and c-myc might play a role in the control of liver regeneration. In order to clarify the inhibitory mechanism of ethanol on hepatocytes proliferation, the expression of c-fos and c-myc and DNA synthesis were investigated. Rats were divided into 4 groups in this study. In the group A and B, rats were given water. In the group C and D, animals received 20% of ethanol ad libitum for 8 weeks. In group B and D, animals were given 33% of ethanol as a single dose of 4g ethanol /kg body weight to study a acute effect of ethanol. DNA synthesis as estimated by ^3H-thymidine incorporation was significantly inhibited only in chronically ethanol-fed rats with additional ethanol administration soon after partial hepatectomy, group D, whereas it was not changed in the other 3 groups. A significant reduction of c-myc transcripts was also found in chronically ethanol-fed rats with acute ethanol administration, group D, while c-fos expression was almost the same in the all groups. It is concluded that the inhibition of liver regeneration by ethanol was observed in chronically ethanol-fed rats with acute ethanol administration, followed by a significant decrease in c-myc expression. This suggested that the reduction of c-myc expression was related to the inhibition of dna synthesis by ethanol.
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Report
(3 results)
Research Products
(11 results)
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[Publications] 古澤俊一,林紀夫,八嶌俊,笠原彰紀,佐々木裕,河野通一,片山和宏,山添光芳,房本英之,佐藤信紘,鎌田武信: 肝臓. 29. 377-381 (1988)
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