Discover the SciOpen Platform and Achieve Your Research Goals with Ease.
Search articles, authors, keywords, DOl and etc.
This study is to explore underlying mechanism of skin wound healing by snakehead fish soup using rat and cell models. We assessed skin wound changes after administering wild and farmed snakehead fish soup intragastrically, then using CCK-8 and scratch tests to evaluate cell proliferation and migration, last assessed vessel tubule formation by HUVEC cells. The results showed that the skin wound healing rates of rats after 14 days of intragastrical administration of farmed and wild snakehead fish soup were 52.71% and 57.76%, respectively, which were substantially greater than the control group (39.84%). With the administration of the soups, the collagen tissue on the skin wound was more homogenous and thicker, and type I collagen was denser. Additionally, interleukin-6 level in rat serum during wound healing was significantly lower, while cyclin-D1 and fibroblast growth factor-2 levels were higher. Furthermore, the soups (particularly at 50 μg/mL) significantly increased the proliferation and migration rates of both the HACAT and NIH3T3 cells, and considerably promoted the tubule formation of HUVEC cells. The findings confirm that the soup can promote skin wound healing and the underlying mechanism involves multiple roles including anti-inflammation, cell proliferation, vessel tubule formation, and collagen expression.
J. Zhang, M. Li, G. N. Zhang, et al., Identification of novel antioxidant peptides from snakehead ( Channa argus) soup generated during gastrointestinal digestion and insights into the anti-oxidation mechanisms, Food. Chem. 337 (2021) 127921. https://doi.org/10.1016/j.foodchem.2020.127921.
N. A. Sahid, F. Hayati, C. V. Rao, et al., Snakehead consumption enhances wound healing? From tradition to modern clinical practice: a prospective randomized controlled trial, Evid.-Based Compl. Alt. 2018 (2018) 3032790. https://doi.org/10.1155/2018/3032790.
M. He, W. Q. Xie, G. Cheng, et al., The therapeutic effects of earthworm extract on deep second-degree burn wound healing, Ann. Palliat. Med. 10(3) (2021) 2869–2879. https://doi.org/10.21037/apm-20-2393.
M. Taniguchi, K. Saito, R. Aida, et al., Wound healing activity and mechanism of action of antimicrobial and lipopolysaccharide-neutralizing peptides from enzymatic hydrolysates of rice bran proteins, J. Biosci. Bioeng. 128(2) (2019) 142–148. https://doi.org/10.1016/j.jbiosc.2019.02.002.
M. T. Ren, T. Yin, J. You, et al., Comparative study of the nutritional composition and antioxidant ability of soups made from wild and farmed snakehead fish ( Channa argus), Foods 11(20) (2022) 3294. https://doi.org/10.3390/foods11203294.
M. C. E. V. Schiassi, V. R. de Souza, A. M. T. Lago, et al., Quality of honeys from different botanical origins, J. Food. Sci. Tech. Mys. 58(11) (2021) 4167–4177. https://doi.org/10.1007/s13197-020-04884-7.
Y. R. Shang, D. W. Li, C. N. Shen, et al., The benefit of microskin in combination with autologous keratinocyte suspension to treat full skin loss in vivo, J. Burn. Care. Res. 38(6) (2017) 348–353. https://doi.org/10.1097/Bcr.0000000000000552.
W. Jeong, C. E. Yang, T. S. Roh, et al., Scar prevention and enhanced wound healing induced by polydeoxyribonucleotide in a rat incisional wound-healing model, Int. J. Mol. Sci. 18(8) (2017) 1698. https://doi.org/10.3390/ijms18081698.
M. E. Rheaume, J. Perreault, D. Fournier, et al., Preparation and growth factor characterization of cord blood-derived plasma, serum, growth factor-rich plasma and induced serum, Cytokine 149 (2022) 155756. https://doi.org/10.1016/j.cyto.2021.155756.
Z. Ru, Y. Hu, S. H. Huang, et al., Bioflavonoid Galangin suppresses hypertrophic scar formation by the TGF-β/smad signaling pathway, Evid.-Based Compl. Alt. 2021 (2021) 2444839. https://doi.org/10.1155/2021/2444839.
M. V. Mouritzen, H. Jenssen, Optimized scratch assay for in vitro testing of cell migration with an automated optical camera, Jove. J. Vis. Exp. 138 (2018) e57691. https://doi.org/10.3791/57691.
F. Y. Li, X. Gou, D. Xu, et al., Improvement of tube formation model of cell: application for acute hypoxia in in vitro study of angiogenesis, Microvasc. Res. 140 (2022) 104297. https://doi.org/10.1016/j.mvr.2021.104297.
E. Park, S. M. Lee, I. K. Jung, et al., Effects of genistein on early-stage cutaneous wound healing, Biochem. Bioph. Res. Co. 410(3) (2011) 514–519. https://doi.org/10.1016/j.bbrc.2011.06.013.
J. L. Chen, M. Jayachandran, B. J. Xu, et al., Sea bass ( Lateolabrax maculatus) accelerates wound healing: a transition from inflammation to proliferation, J. Ethnopharmacol. 236 (2019) 263–276. https://doi.org/10.1016/j.jep.2019.03.012.
S. K. Verma, H. Yaghoobi, P. Slaine, et al., Multi-pin contact drawing enables production of anisotropic collagen fiber substrates for alignment of fibroblasts and monocytes, Colloid. Surface. B 215 (2022) 112525. https://doi.org/10.1016/j.colsurfb.2022.112525.
A. C. L. Campos, A. K. Groth, A. B. Branco, Assessment and nutritional aspects of wound healing, Curr. Opin. Clin. Nutr. 11(3) (2008) 281–288. https://doi.org/10.1097/MCO.0b013e3282fbd35a.
K. Mistry, B. van der Steen, T. Clifford, et al., Potentiating cutaneous wound healing in young and aged skin with nutraceutical collagen peptides, Clin. Exp. Dermatol. 46(1) (2021) 109–117. https://doi.org/10.1111/ced.14392.
M. Ponnusamy, P. F. Li, K. Wang, Understanding cardiomyocyte proliferation: an insight into cell cycle activity, Cell. Mol. Life. Sci. 74(6) (2017) 1019–1034. https://doi.org/10.1007/s00018-016- 2375-y.
C. J. Powers, S. W. Mcleskey, A. Wellstein, Fibroblast growth factors, their receptors and signaling, Endocrine. Related. Cancer. 7(3) (2000) 165–197. https://doi.org/10.1677/erc.0.0070165.
M. Taniguchi, A. Ochiai, T. Namae, et al., The antimicrobial and anti-endotoxic peptide AmyI-1-18 from rice α-amylase and its [N3L] analog promote angiogenesis and cell migration, Peptides. 104 (2018) 78–84. https://doi.org/10.1016/j.peptides.2018.04.017.
M. F. Fu, C. G. Wang, Z. P. Li, et al., Minireview: cyclin D1: normal and abnormal functions, Endocrinology 145(12) (2004) 5439–5447. https://doi.org/10.1210/en.2004-0959.
H. H. Wong, S. H. Seet, C. C. Bascom, et al., Red-COLA1: a human fibroblast reporter cell line for type I collagen transcription, Sci. Rep. Uk. 10(1) (2020) 19723. https://doi.org/10.1038/s41598-020-75683-5.
X. Y. Gao, X. C. Zhang, Y. W. Wang, et al., Effects of morphology and surface hydroxyl on the toxicity of BiOCl in human HaCaT cells, Chemosphere 163 (2016) 438–445. https://doi.org/10.1016/j.chemosphere.2016.08.063.
Y. H. Song, R. S. Maul, C. S. Gerbin, et al., Inhibition of anchorage-independent growth of transformed NIH3T3 cells by epithelial protein lost in neoplasm (EPLIN) requires localization of EPLIN to actin cytoskeleton, Mol. Biol. Cell. 13(4) (2002) 1408–1416. https://doi.org/10.1091/mbc.01-08-0414.
W. J. Yang, Y. N. Yang, J. Cao, et al., Paxillin regulates vascular endothelial growth factor A-induced in vitro angiogenesis of human umbilical vein endothelial cells, Mol. Med. Rep. 11(3) (2015) 1784–1792. https://doi.org/10.3892/mmr.2014.2961.
D. J. Medina-Leyte, M. Domínguez-Pérez, I. Mercado, et al., Use of human umbilical vein endothelial cells (HUVEC) as a model to study cardiovascular disease: a review, Appl. Sci. 10(3) (2020) 938. https://doi.org/10.3390/app10030938.
Z. H. Zheng, M. Q. Li, P. F. Jiang, et al., Peptides derived from sea cucumber accelerate cells proliferation and migration for wound healing by promoting energy metabolism and upregulating the ERK/AKT pathway, Eur. J. Pharmacol. 921 (2022) 174885. https://doi.org/10.1016/j.ejphar.2022.174885.
R. J. Bodnar, L. Satish, C. C. Yates, et al., Pericytes: a newly recognized player in wound healing, Wound. Repair. Regen. 24(2) (2016) 204–214. https://doi.org/10.1111/wrr.12415.
S. B. Huang, Z. C. Hu, P. Wang, et al., Rat epidermal stem cells promote the angiogenesis of full-thickness wounds, Stem. Cell. Res. Ther. 11(1) (2020) 344. https://doi.org/10.1186/s13287-020-01844-y.
D. N. Heo, M. Hospodiuk, I. T. Ozbolat, Synergistic interplay between human MSCs and HUVECs in 3D spheroids laden in collagen/fibrin hydrogels for bone tissue engineering, Acta. Biomater. 95 (2019) 348–356. https://doi.org/10.1016/j.actbio.2019.02.046.
A. Glady, A. Vandebroek, M. Yasui, Human keratinocyte-derived extracellular vesicles activate the MAPKinase pathway and promote cell migration and proliferation in vitro, Inflamm. Regen 41(1) (2021) 4. https://doi.org/10.1186/s41232-021-00154-x.
H. Z. Li, X. Han, K. Y. Zuo, et al., MiR-23b promotes cutaneous wound healing through inhibition of the inflammatory responses by targeting ASK1, Acta. Bioch. Bioph. Sin. 50(11) (2018) 1104–1113. https://doi.org/10.1093/abbs/gmy109.
Food Science of Animal Products published by Tsinghua University Press. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).