Stellera chamaejasme and its constituents induce cutaneous wound healing and anti-inflammatory activities

被引:38
|
作者
Kim, Myungsuk [1 ,2 ]
Lee, Hee Ju [3 ]
Randy, Ahmad [1 ,4 ]
Yun, Ji Ho [1 ,2 ]
Oh, Sang-Rok [2 ]
Nho, Chu Won [1 ,2 ]
机构
[1] Korea Inst Sci & Technol, Nat Prod Res Ctr, Kangnung, South Korea
[2] Korea Inst Sci & Technol, Convergence Res Ctr Smart Farm Solut, Kangnung, South Korea
[3] Korea Inst Sci & Technol, Syst Biotechnol Res Ctr, Kangnung, South Korea
[4] Univ Sci & Technol, Dept Biol Chem, Daejeon, South Korea
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
NITRIC-OXIDE SYNTHASE; GROWTH-FACTOR-BETA; DEPENDENT TRANSCRIPTIONAL ACTIVATION; CATENIN STABILIZATION; CENTELLA-ASIATICA; COLLAGEN; SKIN; CYCLOOXYGENASE-2; DIFFERENTIATION; IDENTIFICATION;
D O I
10.1038/srep42490
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Stellera chamaejasme L. (Thymelaeaceae) is a perennial herb that is widely used in traditional Chinese medicine to treat tumours, tuberculosis and psoriasis. S. chamaejasme extract (SCE) possesses anti-inflammatory, analgesic and wound healing activities; however, the effect of S. chamaejasme and its active compounds on cutaneous wound healing has not been investigated. We assessed full-thickness wounds of Sprague-Dawley (SD) rats and topically applied SCE for 2 weeks. In vitro studies were performed using HaCaT keratinocytes, Hs68 dermal fibroblasts and RAW 264.7 macrophages to determine cell viability (MTT assay), cell migration, collagen expression, nitric oxide (NO) production, prostaglandin E-2 (PGE(2)) production, inflammatory cytokine expression and beta-catenin activation. In vivo, wound size was reduced and epithelisation was improved in SCE-treated SD rats. In vitro, SCE and its active compounds induced keratinocyte migration by regulating the beta-catenin, extracellular signal-regulated kinase and Akt signalling pathways. Furthermore, SCE and its active compounds increased mRNA expression of type I and III collagen in Hs68 fibroblasts. SCE and chamechromone inhibited NO and PGE2 release and mRNA expression of inflammatory mediators in RAW 264.7 macrophages. SCE enhances the motility of HaCaT keratinocytes and improves cutaneous wound healing in SD rats.
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页数:11
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