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Gastroprotective effects of the nonsaponin fraction of Korean Red Ginseng through cyclooxygenase-1 upregulation.
Lee, Jeong-Oog; Kim, Ji Hye; Kim, Sunggyu; Kim, Mi-Yeon; Hong, Yo Han; Kim, Han Gyung; Cho, Jae Youl.
Afiliación
  • Lee JO; Department of Aerospace Information Engineering, Bio-Inspired Aerospace Information Laboratory, Konkuk University, Seoul, Republic of Korea.
  • Kim JH; Department of Integrative Biotechnology, Sungkyunkwan University, Suwon, Republic of Korea.
  • Kim S; Research and Business Foundation, Sungkyunkwan University, Suwon, Republic of Korea.
  • Kim MY; Department of Biocosmetics, Sungkyunkwan University, Suwon, Republic of Korea.
  • Hong YH; School of Systems Biomedical Science, Soongsil University, Seoul, Republic of Korea.
  • Kim HG; Department of Integrative Biotechnology, Sungkyunkwan University, Suwon, Republic of Korea.
  • Cho JY; Department of Integrative Biotechnology, Sungkyunkwan University, Suwon, Republic of Korea.
J Ginseng Res ; 44(4): 655-663, 2020 Jul.
Article en En | MEDLINE | ID: mdl-32617046
BACKGROUND: Korean Red Ginseng is known to exhibit immune-enhancing and anti-inflammatory properties. The immune-enhancing effects of the nonsaponin fraction (NSF) of Korean Red Ginseng have been studied in many reports. However, the gastroprotective effect of this fraction is not fully understood. In this study, we demonstrate the activities of NSF for gastrointestinal protection and its related critical factor. METHODS: The in vitro and in vivo regulatory functions of NSF on cyclooxygenase-1 (COX-1) messenger RNA and protein levels were examined by reverse transcription polymerase chain reaction and immunoblotting analyses. Gastroprotective effects of NSF were investigated by histological score, gastric juice pH, and myeloperoxidase activity on indomethacin-induced, cold stress-induced, and acetylsalicylic acid-induced gastritis and dextran sulfate sodium-induced colitis in in vivo mouse models. RESULTS: NSF did not show cytotoxicity, and it increased COX-1 messenger RNA expression and protein levels in RAW264.7 cells. This upregulation was also observed in colitis and gastritis in vivo models. In addition, NSF treatment in mice ameliorated the symptoms of gastrointestinal inflammation, including histological score, colon length, gastric juice pH, gastric wall thickness, and myeloperoxidase activity. CONCLUSION: These results suggest that NSF has gastroprotective effects on gastritis and colitis in in vivo mouse models through COX-1 upregulation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Ginseng Res Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Ginseng Res Año: 2020 Tipo del documento: Article
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