ArticleScientific reports2017
Stellera chamaejasme and its constituents induce cutaneous wound healing and anti-inflammatory activities.
Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Enhanced Skin-Protective Effects of a NovelJournal of microbiology and biotechnology · 2025Article
- Burn Wound Healing Abilities of a Uronic Acid Containing Exopolysaccharide Produced by the Marine Bacterium Halomonas malpeensis YU-PRIM-29Applied biochemistry and biotechnology · 2024Article
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- Terpenoids from the Roots ofMolecules (Basel, Switzerland) · 2023Article
- Antioxidant and Anti-Inflammatory Activities ofLife (Basel, Switzerland) · 2023Article
- Characterization of Polyphenolic Compounds fromMolecules (Basel, Switzerland) · 2022Article
- Gel formulated withFrontiers in pharmacology · 2022Article
- The Modulatory Influence of Plant-Derived Compounds on Human Keratinocyte Function.International journal of molecular sciences · 2021Review
- Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2019Article
- Isolation of maltol derivatives fromRSC advances · 2019Article
- Exploring Chemical Basis of Toxicity Reduction for Processed Roots ofInternational journal of analytical chemistry · 2019Article
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Authors and funding
6 authors.
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Abstract
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
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