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Perilla frutescens Extracts Protects against Dextran Sulfate Sodium-Induced Murine Colitis: NF-κB, STAT3, and Nrf2 as Putative Targets.
Park, Deung Dae; Yum, Hye-Won; Zhong, Xiancai; Kim, Seung Hyeon; Kim, Seong Hoon; Kim, Do-Hee; Kim, Su-Jung; Na, Hye-Kyung; Sato, Atsuya; Miura, Takehito; Surh, Young-Joon.
Afiliación
  • Park DD; Tumor Microenvironment Global Core Research Center, Seoul National UniversitySeoul, South Korea.
  • Yum HW; Department of Molecular Medicine and Biopharmaceutical Sciences, College of Pharmacy, Seoul National UniversitySeoul, South Korea.
  • Zhong X; Tumor Microenvironment Global Core Research Center, Seoul National UniversitySeoul, South Korea.
  • Kim SH; Tumor Microenvironment Global Core Research Center, Seoul National UniversitySeoul, South Korea.
  • Kim SH; Tumor Microenvironment Global Core Research Center, Seoul National UniversitySeoul, South Korea.
  • Kim DH; Cancer Research Institute, Seoul National UniversitySeoul, South Korea.
  • Kim SJ; Tumor Microenvironment Global Core Research Center, Seoul National UniversitySeoul, South Korea.
  • Na HK; Tumor Microenvironment Global Core Research Center, Seoul National UniversitySeoul, South Korea.
  • Sato A; Tumor Microenvironment Global Core Research Center, Seoul National UniversitySeoul, South Korea.
  • Miura T; Department of Molecular Medicine and Biopharmaceutical Sciences, College of Pharmacy, Seoul National UniversitySeoul, South Korea.
  • Surh YJ; Department of Food Science and Biotechnology, College of Knowledge-Based Services Engineering, Sungshin Women's UniversitySeoul, South Korea.
Front Pharmacol ; 8: 482, 2017.
Article en En | MEDLINE | ID: mdl-28848431
ABSTRACT
Perilla frutescens is a culinary and medicinal herb which has a strong anti-inflammatory and antioxidative effects. In the present study, we investigated the effects of Perilla frutescens extract (PE) against dextran sulfate sodium (DSS)-induced mouse colitis, an animal model that mimics human inflammatory bowel disease (IBD). Five-week-old male ICR mice were treated with a daily dose of PE (20 or 100 mg/kg, p.o.) for 1 week, followed by administration of 3% DSS in double distilled drinking water and PE by gavage for another week. DSS-induced colitis was characterized by body weight loss, colon length shortening, diarrhea and bloody stool, and these symptoms were significantly ameliorated by PE treatment. PE administration suppressed DSS-induced expression of proinflammatory enzymes, including cyclooxygenase-2 and inducible nitric oxide synthase as well as cyclin D1, in a dose-dependent fashion. Nuclear factor-kappa B (NF-κB) and signal transducer and activator of transcription 3 (STAT3) are major transcriptional regulators of inflammatory signaling. PE administration significantly inhibited the activation of both NF-κB and STAT3 induced by DSS, while it elevated the accumulation of Nrf2 and heme oxygenase-1 in the colon. In another experiment, treatment of CCD841CoN human normal colon epithelial cells with PE (10 mg/ml) resulted in the attenuation of the tumor necrosis factor-α-induced expression/activation of mediators of proinflammatory signaling. The above results indicate that PE has a preventive potential for use in the management of IBD.
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pharmacol Año: 2017 Tipo del documento: Article País de afiliación: Corea del Sur

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pharmacol Año: 2017 Tipo del documento: Article País de afiliación: Corea del Sur