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  2. Catechin-7-O-β-D-glucopyranoside isolated from the seed of Phaseolus calcaratus Roxburgh ameliorates experimental colitis in rats

Catechin-7-O-β-D-glucopyranoside isolated from the seed of Phaseolus calcaratus Roxburgh ameliorates experimental colitis in rats

  • Int Immunopharmacol. 2015 Dec;29(2):521-527. doi: 10.1016/j.intimp.2015.10.003.
Sung-Ho Kook 1 Ki Choon Choi 2 Seong-Wan Cho 3 Hyoung-Kwon Cho 4 Kyung Dong Lee 5 Jeong-Chae Lee 6
Affiliations

Affiliations

  • 1 Department of Bioactive Material Sciences, Institute of Molecular Biology and Genetics, Institute of Oral Biosciences and School of Dentistry, Chonbuk National University, Jeonju 561-756, South Korea.
  • 2 Grassland and forage division, National Institute of Animal Science, RDA, Cheonan 330-801, South Korea.
  • 3 Department of Pharmaceutical Engineering, Konyang University, Nonsan 320-711, South Korea.
  • 4 Center for Health Care Technology Development, HanPoong Pharmaceutical Co. Ltd., Jeonju 561-201, South Korea.
  • 5 Department of Oriental Medicine Materials, Dongsin University, Naju 520-714, South Korea.
  • 6 Department of Bioactive Material Sciences, Institute of Molecular Biology and Genetics, Institute of Oral Biosciences and School of Dentistry, Chonbuk National University, Jeonju 561-756, South Korea. Electronic address: leejc88@jbnu.ac.kr.
Abstract

The seeds of Phaseolus calcaratus Roxburgh (PHCR) are common legumes that comprise part of the daily diet in Chinese and Korean culture. Recent findings highlight anti-inflammatory and anti-septic potentials of catechin-7-O-β-D-glucopyranoside (CGP) isolated from PHCR seeds. We investigated the intestinal anti-inflammatory activity and associated mechanisms of CGP using a rat model of trinitrobenzenesulfonic acid (TNBS)-induced colitis. Oral treatment with CGP (10mg/kg body weight) suppressed body weight loss and intestinal inflammatory damages in TNBS-induced colitic rats. This treatment reduced myeloperoxidase activity and malondialdehyde level, but increased glutathione level in the TNBS colitic rats. CGP treatment also inhibited the TNBS-mediated increases in nitric oxide synthase, cyclooxygenase-2, interleukin-1β, tumor necrosis factor-α, intercellular adhesion molecule-1, and monocyte chemotactic protein-1 proteins or mRNA levels. This inhibition was accompanied by the increased mRNA levels of mucins MUC2 and MUC3. The CGP treatment prevented phosphorylation of p38 mitogen-activated protein kinase, IκB-α, and DNA-nuclear factor-κB binding, all of which were increased in the inflamed colons of TNBS-treated rats. Furthermore, oral administration with a crude PHCR butanol extract (100mg/kg body weight) which contains 1.5% of CGP showed intestinal anti-inflammatory potentials similar to that of CGP. Collectively, our current findings suggest that CGP or CGP-containing PHCR seeds may have favorable effects on intestinal inflammatory diseases.

Keywords

Catechin-7-O-β-d-glucopyranoside; Intestinal anti-inflammation; Phaseolus calcaratus R; Ulcerative colitis.

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