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乙酰辅酶 A 羧化酶 1 和 2 的抑制作用可改善 MC4R 基因敲除非酒精性脂肪性肝炎小鼠模型的脂肪变性和肝纤维化。

Acetyl-CoA carboxylase 1 and 2 inhibition ameliorates steatosis and hepatic fibrosis in a MC4R knockout murine model of nonalcoholic steatohepatitis.

机构信息

Department of Integrated Biology, Axcelead Drug Discovery Partners, Inc., Fujisawa, Kanagawa, Japan.

Gastroenterology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Cambridge, Massachusetts, United States of America.

出版信息

PLoS One. 2020 Jan 28;15(1):e0228212. doi: 10.1371/journal.pone.0228212. eCollection 2020.

Abstract

Acetyl-CoA carboxylase (ACC) catalyzes the rate-limiting step in de novo lipogenesis, which is increased in the livers of patients with nonalcoholic steatohepatitis. GS-0976 (firsocostat), an inhibitor of isoforms ACC1 and ACC2, reduced hepatic steatosis and serum fibrosis biomarkers such as tissue inhibitor of metalloproteinase 1 in patients with nonalcoholic steatohepatitis in a randomized controlled trial, although the impact of this improvement on fibrosis has not fully been evaluated in preclinical models. Here, we used Western diet-fed melanocortin 4 receptor-deficient mice that have similar phenotypes to nonalcoholic steatohepatitis patients including progressively developed hepatic steatosis as well as fibrosis. We evaluated the effects of ACC1/2 inhibition on hepatic fibrosis. After the confirmation of significant hepatic fibrosis with a 13-week pre-feeding, GS-0976 (4 and 16 mg/kg/day) treatment for 9 weeks lowered malonyl-CoA and triglyceride content in the liver and improved steatosis, histologically. Furthermore, GS-0976 reduced the histological area of hepatic fibrosis, hydroxyproline content, mRNA expression level of type I collagen in the liver, and plasma tissue metalloproteinase inhibitor 1, suggesting an improvement of hepatic fibrosis. The treatment with GS-0976 was also accompanied by reductions of plasma ALT and AST levels. These data demonstrate that improvement of hepatic lipid metabolism by ACC1/2 inhibition could be a new option to suppress fibrosis progression as well as to improve hepatic steatosis in nonalcoholic steatohepatitis.

摘要

乙酰辅酶 A 羧化酶 (ACC) 催化从头合成脂肪的限速步骤,该步骤在非酒精性脂肪性肝炎患者的肝脏中增加。GS-0976(非司他特)是同工酶 ACC1 和 ACC2 的抑制剂,在一项随机对照试验中,它可减少非酒精性脂肪性肝炎患者的肝脂肪变性和血清纤维化生物标志物,如组织金属蛋白酶抑制剂 1,但这种改善对纤维化的影响在临床前模型中尚未得到充分评估。在这里,我们使用了黑素皮质素 4 受体缺陷型小鼠,这些小鼠在饮食诱导下表现出类似于非酒精性脂肪性肝炎患者的表型,包括逐渐发展的肝脂肪变性和纤维化。我们评估了 ACC1/2 抑制对肝纤维化的影响。在确认经过 13 周预喂养后出现明显的肝纤维化后,GS-0976(4 和 16mg/kg/天)治疗 9 周可降低肝脏中的丙二酰辅酶 A 和甘油三酯含量,并改善脂肪变性,组织学上也得到改善。此外,GS-0976 降低了肝纤维化的组织学面积、羟脯氨酸含量、肝脏中 I 型胶原的 mRNA 表达水平和血浆组织金属蛋白酶抑制剂 1,表明肝纤维化得到改善。GS-0976 的治疗还伴有血浆 ALT 和 AST 水平的降低。这些数据表明,通过 ACC1/2 抑制改善肝脂质代谢可能是抑制纤维化进展和改善非酒精性脂肪性肝炎肝脂肪变性的新选择。

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