日本語フィールド
著者：Bogahawaththa, Sudarma; Kawamura, Tomoaki; Bandaranayake, Udari; Hirakawa, Tomoaki; Yamada, Goki; Ishino, Hana; Hirohashi, Tsuzumi; Kawaguchi, Shin Ichi; Wijesundera, Kavindra K.; Wijayagunawardane, Missaka P.B.; Ishimaru, Kanji; Kodithuwakku, Suranga P.; Tsujita, Tadayuki題名：Identification and mechanistic investigation of ellagitannins from Osbeckia octandra that attenuate liver fibrosis via the TGF-β/SMAD signaling pathway発表情報：Bioscience, biotechnology, and biochemistry 巻: 87 号: 11 ページ: 1295 - 1309キーワード：概要：Fibrosis is a major problem in chronic liver disease with limited treatment options due to its complex nature. Herbal medicines are often used as an alternative. The aim of this study was to investigate the therapeutic potential of Osbeckia octandra and to identify its active compounds and regulatory pathways. The effects of crude leaf suspension and boiled leaf extract were investigated in an animal model, and the extract was found to be the more effective treatment. Three major bioactive compounds, pedunculagin, casuarinin, and gallic acid, were isolated from the extract using the hepatic stellate cell line, LX-2-based antifibrotic effect evaluation system. The results showed that all these compounds ameliorated LX-2 in fibrotic state. This inhibitory mechanism was confirmed through the TGF-β/SMAD signaling pathway. Collectively, the presence of these compounds in O. octandra suggests its potential as a treatment for liver fibrosis.抄録：英語フィールド
Author：Bogahawaththa, Sudarma^D; Kawamura, Tomoak^Mi; Bandaranayake, Udari; Hirakawa, Tomoaki^D; Yamada, Goki^D; Ishino, Hana^M; Hirohashi, Tsuzumi^M; Kawaguchi, Shin Ichi; Wijesundera, Kavindra K.; Wijayagunawardane, Missaka P.B.; Ishimaru, Kanji; Kodithuwakku, Suranga P.; Tsujita, TadayukiTitle：Identification and mechanistic investigation of ellagitannins from Osbeckia octandra that attenuate liver fibrosis via the TGF-β/SMAD signaling pathwayAnnouncement information:Bioscience, biotechnology, and biochemistry Vol: 87 Issue: 11 Page: 1295 - 1309An abstract：Fibrosis is a major problem in chronic liver disease with limited treatment options due to its complex nature. Herbal medicines are often used as an alternative. The aim of this study was to investigate the therapeutic potential of Osbeckia octandra and to identify its active compounds and regulatory pathways. The effects of crude leaf suspension and boiled leaf extract were investigated in an animal model, and the extract was found to be the more effective treatment. Three major bioactive compounds, pedunculagin, casuarinin, and gallic acid, were isolated from the extract using the hepatic stellate cell line, LX-2-based antifibrotic effect evaluation system. The results showed that all these compounds ameliorated LX-2 in fibrotic state. This inhibitory mechanism was confirmed through the TGF-β/SMAD signaling pathway. Collectively, the presence of these compounds in O. octandra suggests its potential as a treatment for liver fibrosis.