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Lee, Y.-J., Y.-N. Jang, et al, “Caffeoylquinic Acid-Rich Extract of Aster glehni F. Schmidt Ameliorates Nonalcoholic Fatty Liver through the Regulation of PPARδ and Adiponectin in ApoE KO Mice,” PPAR research, Oct.2017.

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Nrf2/HO-1-inductive Preventive Effect of 3,5-dicaffeoylquinic Acid, Antioxidant Compound from Green Coffee Beans, on Dimethylnitrosamine-induced Liver Fibrosis in Rats

1Department of Biomedical Science and Program in Biomedical Science & Engineering, Inha University College of Medicine, Incheon 22212, Republic of Korea

2Division of Gastroenterology & Hepatology, Inha University Hospital, Incheon 22332, Republic of Korea

3Inha Institute of Aerospace Medicine, Inha University College of Medicine, Incheon 22212, Republic of Korea


Journal of Food and Nutrition Research. 2020, Vol. 8 No. 9, 528-535
DOI: 10.12691/jfnr-8-9-9
Copyright © 2020 Science and Education Publishing

Cite this paper:
Min A Kim, Chul-Jun Lee, Seon-ah Park, Do Hun Kim, Don-Haeng Lee, Su-Geun Yang. Nrf2/HO-1-inductive Preventive Effect of 3,5-dicaffeoylquinic Acid, Antioxidant Compound from Green Coffee Beans, on Dimethylnitrosamine-induced Liver Fibrosis in Rats. Journal of Food and Nutrition Research. 2020; 8(9):528-535. doi: 10.12691/jfnr-8-9-9.

Correspondence to: Su-Geun  Yang, Department of Biomedical Science and Program in Biomedical Science & Engineering, Inha University College of Medicine, Incheon 22212, Republic of Korea. Email: sugeun.yang@inha.ac.kr

Abstract

In this study, we investigated the hepatoprotective properties of 3,5-dicaffeoylquinic acid (DQA), a polyphenolic compound from green coffee beans, against dimethylnitrosamine (DMN)-induced hepatic fibrosis rat models. DQA, up to 10 μM concentration, did not exhibit any cytotoxic effect on Chang liver cells and Huh7 cells. DMN-treated rats showed typical biological symptoms of hepatic fibrosis, i.e., loss of body weight and pathological elevation of serum biomarkers for hepatic function. However, oral administration of DQA recovered body weight, and maintained serum biochemical markers such as albumin, bilirubin, ALP, ALT and AST in the normal range. Notably, histological and western assay proved DQA significantly alleviated collagen accumulation (α-smooth muscle actin, alpha 1 collagen type I) in liver tissue. The upregulated tissue expression of erythroid 2–related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) suggested DQA upregulated the representative antioxidant enzymes and ameliorated the progression of hepatic fibrosis in DMN-treated rats.

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