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ชื่อเรื่อง: | An ethyl-acetate fraction of Holothuria scabra modulates inflammation in vitro through inhibiting the production of nitric oxide and pro-inflammatory cytokines via NF-κB and JNK pathways |
ผู้แต่ง: | Pranweerapaiboon K. Apisawetakan S. Nobsathian S. Itharat A. Sobhon P. Chaithirayanon K. |
Keywords: | acetic acid ethyl ester animal extract antiinflammatory agent butanol cytokine gallic acid glycoside hexane Holothuria scabra extract I kappa B immunoglobulin enhancer binding protein inducible nitric oxide synthase interleukin 1beta Janus kinase lipopolysaccharide messenger RNA mitogen activated protein kinase p38 nitric oxide phenol derivative prostaglandin E2 STAT3 protein terpene triterpene tumor necrosis factor unclassified drug animal cell antiinflammatory activity Article cell viability assay comparative study controlled study cytokine production cytokine release cytotoxicity down regulation drug megadose enzyme linked immunosorbent assay Holothuria Holothuria scabra in vitro study mRNA expression level MTT assay nonhuman priority journal protein expression protein phosphorylation proton nuclear magnetic resonance RAW 264.7 cell line |
วันที่เผยแพร่: | 2020 |
บทคัดย่อ: | Sea cucumber, Holothuria scabra, is an echinoderm marine animal that has long been used as a traditional therapeutic in various diseases due to its chemical composition and protein enrichment. Many researchers have extensively studied the efficacy of sea cucumber extracts for many health benefits in recent years. Inflammation is a complex process involved in pro-/anti-inflammatory cytokine products. However, the role of the H. scabra extracts in anti-inflammation and its molecular regulations has not been apparently elucidated yet. In this study, we investigated the anti-inflammatory effect of H. scabra extracts by using lipopolysaccharide (LPS) from E. coli to induce an inflammatory response in RAW264.7 macrophage. It was found that ethyl acetate fraction of H. scabra extracts (EAHS) inhibited pro-inflammatory cytokines synthesis at both the transcriptional and translational levels, notably nitric oxide (NO), inducible nitric oxide synthase (iNOS), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and prostaglandin E2 (PGE2). In addition, EAHS was able to downregulate IκB/NF-κB, and JNK expressions. These effects may be influenced by high contents of phenolic compound and triterpene glycosides in EAHS. Therefore, EAHS might have the potential to be developed as a natural anti-inflammatory agent. © 2019, Springer Nature Switzerland AG. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/11873 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85076098030&doi=10.1007%2fs10787-019-00677-3&partnerID=40&md5=10de9e5886bc049b19960a6299016caa |
ISSN: | 9254692 |
Appears in Collections: | Scopus 1983-2021 |
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