Chymase inhibitor prevents the development and progression of non-alcoholic steatohepatitis in rats fed a high-fat and high-cholesterol diet

被引:19
作者
Miyaoka, Yuta [1 ]
Jin, Denan [2 ]
Tashiro, Keitaro [1 ]
Komeda, Koji [1 ]
Masubuchi, Shinsuke [1 ]
Hirokawa, Fumitoshi [1 ]
Hayashi, Michihiro [1 ]
Takai, Shinji [2 ]
Uchiyama, Kazuhisa [1 ]
机构
[1] Osaka Med Coll, Dept Gen & Gastroenterol Surg, Takatsuki, Osaka 5698686, Japan
[2] Osaka Med Coll, Grad Sch Med, Dept Innovat Med, 2-7 Daigaku Machi, Takatsuki, Osaka 5698686, Japan
基金
日本学术振兴会;
关键词
Chymase; Inhibitor; Liver failure; Non-alcoholic steatohepatitis; Rat; DEPENDENT MATRIX-METALLOPROTEINASE-9 ACTIVATION; CHRONIC LIVER-DISEASES; HAMSTERS; FIBROSIS; INFLAMMATION; THERAPY; FAILURE; COLITIS; INJURY; MODEL;
D O I
10.1016/j.jphs.2017.04.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of the chymase inhibitor TY-51469 on the development and progression of non-alcoholic steatohepatitis (NASH) was evaluated in rats fed a high-fat and high-cholesterol (HFC) diet. To evaluate the preventive effect of TY-51469 on the development of NASH, stroke-prone spontaneously hypertensive rat 5 (SHRSP5)/Dmcr rats were fed either a normal or HFC diet for 8 weeks, and concurrently administered either placebo or TY-51469 (1 mg/kg per day). To evaluate the effect of TY-51469 on the survival rate, TY-51469 was administered either concurrently with HFC diet (pretreated group) or 8 weeks after HFC diet at which point NASH had developed (posttreated group). Eight weeks after HFC diet, significant increases of steatosis, fibrosis and chymase-positive cells were observed in liver from the placebo-treated rats. Significant increases of myeloperoxidase, transforming growth factor-beta, matrix metalloproteinase-9, and collagen I mRNA levels were also observed. However, all parameters were significantly attenuated in the TY-51469-treated group. A survival rate of the placebo-treated group fed the HFC diet was 0% at 14 weeks. In comparison, the rates of TY-51469-pretreated and TY-51469-posttreated groups were 100% and 50% at 14 weeks, respectively. Chymase inhibitor may be applicable to preventing the development and progression of NASH. (C) 2017 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society.
引用
收藏
页码:139 / 146
页数:8
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