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Jolkinolide B Ameliorates Liver Inflammation and Lipogenesis by Regulating JAK/STAT3 Pathway

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机构: [1]Chungbuk Natl Univ, Coll Pharm & Med Res Ctr, Cheongju 28160, South Korea [2]Duksung Womens Univ, Coll Pharm, Seoul 01369, South Korea [3]Shanghai Jiao Tong Univ, Sch Med, Shanghai Tongren Hosp, Hongqiao Int Inst Med,Shanghai Inst Immunol,Dept I, Shanghai 200025, Peoples R China
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关键词: MASLD Jolkinolide B Lipid accumulation Inflammation

摘要:
Hepatic dysregulation of lipid metabolism exacerbates inflammation and enhances the progression of metabolic dysfunction-associated steatotic liver disease (MASLD). STAT3 has been linked to lipid metabolism and inflammation. Jolkinolide B (JB), derived from Euphorbia fischeriana, is known for its pharmacological anti-inflammatory and anti-tumor properties. Therefore, this study investigated whether JB affects MASLD prevention by regulating STAT3 signaling. JB attenuated steatosis and inflammatory responses in palmitic acid (PA)-treated hepatocytes. Additionally, JB treatment reduced the mRNA expression of de-novo lipogenic genes, such as acetyl-CoA carboxylase and stearoyl-CoA desaturase 1. Interestingly, JB-mediated reduction in inflammation and lipogenesis was dependent on STAT3 signaling. JB consistently modulated mitochondrial dysfunction and the mRNA expression of inflammatory cytokines by inhibiting PA-induced JAK/STAT3 activation. This study suggests that JB is a potential therapeutic agent to prevent major stages of MASLD through inhibition of JAK/STAT3 signaling in hepatocytes.

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出版当年[2023]版:
大类 | 3 区 医学
小类 | 3 区 药学
最新[2023]版:
大类 | 3 区 医学
小类 | 3 区 药学
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出版当年[2022]版:
Q2 PHARMACOLOGY & PHARMACY
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Q2 PHARMACOLOGY & PHARMACY

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第一作者机构: [1]Chungbuk Natl Univ, Coll Pharm & Med Res Ctr, Cheongju 28160, South Korea
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