Anti-inflammatory activity of ethanol extract derived from Phaseolus angularis beans
- Authors
- Yu, Tao; Ahn, Hyo Min; Shen, Ting; Yoon, Keejung; Jang, Hyun-Jae; Lee, Yong Jin; Yang, Hyun Mo; Kim, Jae Hun; Kim, Changhyuk; Han, Moon Hi; Cha, Sang-hun; Kim, Tae Wong; Kim, Sun Young; Lee, Jaehwi; Cho, Jae Youl
- Issue Date
- Oct-2011
- Publisher
- ELSEVIER IRELAND LTD
- Keywords
- Phaseolus angularis; Macrophages; Inflammatory Mediators; NF-B; CREB; Syk; p38
- Citation
- JOURNAL OF ETHNOPHARMACOLOGY, v.137, no.3, pp 1197 - 1206
- Pages
- 10
- Journal Title
- JOURNAL OF ETHNOPHARMACOLOGY
- Volume
- 137
- Number
- 3
- Start Page
- 1197
- End Page
- 1206
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/21175
- DOI
- 10.1016/j.jep.2011.07.048
- ISSN
- 0378-8741
- Abstract
- Ethnopharmacological significance: Phaseolus angularis Wight (adzuki bean) is an ethnopharmacologically well-known folk medicine that is prescribed for infection, edema, and inflammation of the joints, appendix, kidney and bladder in Korea, China and Japan. Aim of study: The anti-inflammatory effect of this plant and its associated molecular mechanisms will be investigated. Materials and methods: The immunomodulatory activity of Phaseolus angularis ethanol extract (Pa-EE) in toll like receptor (TLR)-activated macrophages induced by ligands such as lipopolysaccharide (LPS), Poly (I:C), and pam3CSK was investigated by assessing nitric oxide (NO) and prostaglandin (PG)E-2 levels. To identify which transcription factors such as nuclear factor (NF)-kappa B and their signaling enzymes can be targeted to Pa-EE, biochemical approaches including reporter gene assays, immunoprecipitation, kinase assays, and immunoblot analyses were also employed. Finally, whether Pa-EE was orally available, ethanol (EtOH)/hydrochloric acid (HCl)-induced gastritis model in mice was used. Results: Pa-EE dose-dependently suppressed the release of PGE(2) and NO in LPS-, Poly(I:C)-, and pam3CSK-activated macrophages. Pa-EE strongly down-regulated LPS-induced mRNA expression of inducible NO synthase (iNOS) and cyclooxygenase (COX)-2. Interestingly, Pa-EE markedly inhibited NF-kappa B, activator protein (AP)-1, and cAMP response element binding protein (CREB) activation; further, according to direct kinase assays and immunoblot analyses. Pa-EE blocked the activation of the upstream signaling molecules spleen tyrosine kinase (Syk), p38, and transforming growth factor beta-activated kinase 1 (TAK1). Finally, orally administered Pa-EE clearly ameliorated EtOH/HCl-induced gastritis in mice. Conclusion: Our results suggest that Pa-EE can be further developed as a promising anti-inflammatory remedy because it targets multiple inflammatory signaling enzymes and transcription factors. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
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