New development of animal model of non-obese nonalcoholic steatohepatitis and its corrective establishment
Project/Area Number |
16K00852
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Eating habits
|
Research Institution | Kagawa University |
Principal Investigator |
|
Project Period (FY) |
2016-04-01 – 2019-03-31
|
Project Status |
Completed (Fiscal Year 2018)
|
Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2018: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2017: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2016: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
|
Keywords | 非アルコール性脂肪性肝炎(NASH) / 脂肪肝 / 肥満症 / ミフェプリストン / グルココルチコイド / 肝星状細胞 / 肝非実質細胞 / 肥満 / 受容体遮断薬 / PPARγ受容体 / 糖尿病 / 生理学 / 薬理学 / 栄養学 |
Outline of Final Research Achievements |
Mifepristone, a putative steroid receptor antagonist, clinically serves as an anti-cancer agent. However, the metabolic effects of long-term treatment with mifepristone remain largely unclear. This study aimed to determine whether mifepristone influences glucose metabolism and hepatic steatosis in healthy mice fed with regular diet (RD). The 12-week administration of mifepristone as a mixture with RD markedly increased a percentage of liver wet weight, the level of fasting blood glucose, the amount of food consumption and a percentage of body fat, in a dose-dependent manner ranging from 0.1 to 30 mg/kg/day. Bodipy 493/503 staining of liver specimens revealed the development of hepatic steatosis. Moreover, it increased in the expression of both gene and protein which have a regulation on glucose metabolism in a liver of the mifepristone fed mouse. These results suggest that long term administration of mifepristone leads to the development of non-obese non-alcoholic fatty liver disease.
|
Academic Significance and Societal Importance of the Research Achievements |
肥満が危険因子の一つである非アルコール性脂肪性肝炎(NASH: Nonalcoholic steatohepatitis)の患者数は、肥満の程度が比較的軽い日本において増加している。この発症メカニズムを解明するための最適な非肥満非アルコール性脂肪肝モデル動物の開発を行った。 従来、非肥満NASHモデル動物には、高コレステロール食事誘発性モデルの報告はあるが、通常食を使用したモデル動物の報告はない。本研究において、通常食と小分子化合物を用いた新しい非肥満非アルコール性脂肪肝モデル動物を確立することができ、非肥満者におけるNASHの病態解明、新規治療標的の探索および薬効評価に有用であると考えられる。
|
Report
(4 results)
Research Products
(10 results)