Bamboo Stems ( Phyllostachys nigra variety henosis) Containing Polyphenol Mixtures Activate Nrf2 and Attenuate Phenylhydrazine-Induced Oxidative Stress and Liver Injury

• Published in: Nutrients 2019-01, Vol.11 (1), p.114
• Main Authors: Yang, Ji Hye, Choi, Moon-Hee, Na, Chang-Su, Cho, Sam Seok, Kim, Jae Hoon, Ku, Sae Kwang, Cho, Il Je, Shin, Hyun-Jae, Ki, Sung Hwan
• Format: Article
• Language: English
• Subjects: Acids; Anemia; Antioxidants; Apoptosis; bamboo stems; Drug development; Flavonoids; Food; Functional foods & nutraceuticals; Hemolytic anemia; Homeostasis; In vivo methods and tests; Iron; iron overload; Kinases; Liver; Liver diseases; liver injury; Nrf2; Occupational health; Oxidative stress; PN3; Polyphenols; Proteins; Stems; Transcription factors
• ISSN: 2072-6643; 2072-6643
• DOI: 10.3390/nu11010114

This study was designed to investigate the hepatoprotective effect of bamboo stems using in vitro and in vivo experimental liver damage models. Ethyl acetate fraction of 80% ethanol extract of stem (PN3) containing polyphenols had a higher reporter gene activity as monitored by the activity of the NF-E2-related factor (Nrf2) antioxidant pathway in cells in comparison to extracts from other species and under other conditions. The Nrf2 was translocated from the cytosol to the nucleus in response to PN3, followed by induction of the Nrf2 target gene expression, including , , and in HepG2 cells. Phosphorylation of Nrf2 in HepG2 cells was enhanced in PN3, which was mediated by PKCδ, ERK, and p38 MAPK. Consequently, PN3 inhibited arachidonic acid (AA) + iron-induced reactive oxygen species generation and glutathione depletion, and, thus, highlighted their role in cytotoxicity. Treatment with major polyphenols of PN3, including catechin, chlorogenic acid, caffeic acid, and -coumaric acid, also improved AA + iron-mediated oxidative stress and, thus, improved cell viability. Treatment with phenylhydrazine in mice, i.e., the iron overload liver injury model, increased plasma alanine aminotransferase and aspartate aminotransferase levels and changed histological features in mice-a response that was almost completely blocked by PN3 administration. Moreover, PN3 extract mitigated phenylhydrazine-induced oxidative stress and inflammatory responses. Conclusively, PN3 can exert a hepatoprotective effect against iron overload-induced acute liver damage due to its antioxidant properties.