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Sesamin ameliorates nonalcoholic steatohepatitis through inhibiting hepatocyte pyroptosis in vivo and in vitro

Affiliation
Department of Gastroenterology ,The First Affiliated Hospital of Wannan Medical College ,Yijishan Hospital ,Wuhu ,China
Zhang, Teng;
Affiliation
Department of Cardiology ,Suzhou Hospital of Anhui Medical University ,Suzhou ,China
Zhou, Yong;
Affiliation
Department of Gastroenterology ,The First Affiliated Hospital of Wannan Medical College ,Yijishan Hospital ,Wuhu ,China
Zhang, Yan;
Affiliation
Department of Gerontology ,Geriatric Endocrinology Unit ,The First Affiliated Hospital of Wannan Medical College ,Yijishan Hospital ,Wuhu ,China
Wang, De-Guo;
Affiliation
School of Pharmacy ,Anhui Innovative Center for Drug Basic Research of Metabolic Diseases ,Wannan Medical College ,Wuhu ,China
Lv, Qiu-Yue;
Affiliation
Department of Gastroenterology ,The First Affiliated Hospital of Wannan Medical College ,Yijishan Hospital ,Wuhu ,China
Wang, Wen;
Affiliation
Anhui Provincial Key Laboratory of Molecular Enzymology and Mechanism of Major Diseases ,College of Life Sciences ,Anhui Normal University ,Wuhu ,China
Bai, Ya-Ping;
Affiliation
Department of Gerontology ,Geriatric Endocrinology Unit ,The First Affiliated Hospital of Wannan Medical College ,Yijishan Hospital ,Wuhu ,China
Hua, Qiang;
Affiliation
School of Pharmacy ,Anhui Innovative Center for Drug Basic Research of Metabolic Diseases ,Wannan Medical College ,Wuhu ,China
Guo, Li-Qun

Sesamin (Ses) is a natural lignan abundantly present in sesame and sesame oil. Pyroptosis, a newly identified type of pro-inflammatory programmed necrosis, contributes to the development of non-alcoholic steatohepatitis (NASH) when hepatocyte pyroptosis is excessive. In this study, Ses treatment demonstrated an improvement in hepatic damage in mice with high-fat, high-cholesterol diet-induced NASH and palmitate (PA)-treated mouse primary hepatocytes. Notably, we discovered, for the first time, that Ses could alleviate hepatocyte pyroptosis both in vivo and in vitro . Furthermore, treatment with phorbol myristate acetate, a protein kinase Cδ (PKCδ) agonist, increased PKCδ phosphorylation and attenuated the protective effects of Ses against pyroptosis in PA-treated mouse primary hepatocytes. Mechanistically, Ses treatment alleviated hepatocyte pyroptosis in NASH, which was associated with the regulation of the PKCδ/nod-like receptor family CARD domain-containing protein 4/caspase-1 axis. This study introduces a novel concept and target, suggesting the potential use of functional factors in food to alleviate liver damage caused by NASH.

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License Holder: Copyright © 2024 Zhang, Zhou, Zhang, Wang, Lv, Wang, Bai, Hua and Guo.

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