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Preventive effects of Korean red ginseng on experimentally induced colitis and colon carcinogenesis

Cited 3 time in Web of Science Cited 4 time in Scopus
Authors

Shin, Hoon-Jeong; Kim, Do-Hee; Zhong, Xiancai; Yum, Hye-Won; Kim, Su-Jung; Chun, Kyung-Soo; Na, Hye-Kyung; Surh, Young-Joon

Issue Date
2020-05
Publisher
Elsevier BV
Citation
Journal of Traditional and Complementary Medicine, Vol.10 No.3, pp.198-206
Abstract
Korean Red Ginseng (KRG) exerts chemopreventive effects on experimentally induced carcinogenesis through multiple mechanisms. In this study, we investigated effects of KRG on dextran sulfate sodium (DSS)-induced colitis and azoxymethane (AOM) plus DSS-induced colon carcinogenesis in mice. Male C57BL/6J mice were fed diet containing 1% KRG or a standard diet throughout the experiment. The mouse colitis was induced by administration of 3% DSS in drinking water for 1 week. DSS caused body weight loss, diarrhea, rectal bleeding and colon length shortening, and all these symptoms were ameliorated by KRG treatment. KRG inhibited DSS-induced expression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) by suppressing activation of nuclear factor-kappa B (NF-kappa B) and signal transducer and activation of transcription 3 (STAT3). In another experiment, colon carcinogenesis was initiated by single intraperitoneal injection of AOM (10 mg/kg) and promoted by 2% DSS in drinking water. KRG administration relieved the symptoms of colitis and reduced the incidence, the multiplicity and the size of colon tumor. The up-regulation of COX-2, iNOS, c-Myc and Cyclin D1 by AOM plus DSS was attenuated in KRG fed mice which was associated with suppression of NF-kappa B and STAT3 activation. These results suggest that KRG is a potential candidate for chemoprevention of inflammation-associated cancer in the colon. (C) 2020 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC.
ISSN
2225-4110
URI
https://hdl.handle.net/10371/172808
DOI
https://doi.org/10.1016/j.jtcme.2020.04.004
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