Camellia cake extracts reduce burn injury through suppressing inflammatory responses and enhancing collagen synthesis

  • Yuxia Liu
  • Xiaomei Xiao
  • Luling Ji
  • Lu Xie
  • Suzhen Wu
  • Zhiping Liu
Keywords: Camellia cake extracts; Burn injury; Inflammatory response; Collagen

Abstract

Background: Burn injury accidents happen in our daily life, and the burn mortality is especially high in the low-to-middle-income countries. Camellia cake extracts (CCEs) are compound extracts from Camellia cake, and the major ingredients in CCEs may have antimicrobial, anti-oxidative, and anti-inflammatory effects. However, the effects of CCEs on burn inflammation and injury remain unknown.

Objective: This study is to investigate the effects of CCEs in burn injury and explore its mechanism.

Design: First, CCEs were identified to mainly contain camelliaside A and B using Ultra High Performance Liquid Chromatography-Time of Flight Mass Spectrometer (UHPLC-TOF-MS) method. Second, the CCEs’ effect on burn was tested. Burn was induced by boiling water in mice, and then CCEs (30, 50, and 100 mg/mL) were applied on the damaged skin at 3, 7, and 14 days after burn induction.

Results: The results showed that CCEs protected the skin from burn-induced inflammation and enhanced the wound healing in a dose-dependent manner. CCEs decreased the expression levels of various cytokines including IL-6, TNF-α, IL-1β, MCP-1, TGF-β, and IL-10, as well as inflammatory related factors iNOS. Moreover, CCEs increased the levels of collagens, including the mRNA of COLα-1 and COL-3, and inhibited the mRNA of MMP-1 and TIMP-1, and increased the collagen staining. CCEs also reversed the impairment of activity levels of anti-oxidative enzymes. Furthermore, CCEs suppressed the gene expression of pro-inflammatory cytokines in LPS-stimulated human skin keratinocyte, possibly through inhibiting NF-κB signaling pathway. In addition, toxicological safety experiments on CCEs showed that the oral median lethal dose (LD50) was 2,000 mg/kg, the percutaneous LD50 was greater than 2,000 mg/kg, and CCEs did not cause gene mutation.

Conclusion: CCEs exert a potent anti-inflammatory effect against burn damage in mice. And toxicological safety experiments suggest that CCEs are safe for usage.

Downloads

Download data is not yet available.

References


  1. Rowan MP, Cancio LC, Elster EA, Burmeister DM, Rose LF, Natesan S, et al. Burn wound healing and treatment: review and advancements. Crit Care 2015; 19: 243. doi: 10.1186/s13054-015-0961-2

  2. Burns W. WHO; 2016. Available from: http://www.who.int/mediacentre/factsheets/fs365/en/ [cited 5 December 2018].

  3. Smolle C, Cambiaso-Daniel J, Forbes AA, Wurzer P, Hundeshagen G, Branski LK, et al. Recent trends in burn epidemiology worldwide: a systematic review. Burns 2017; 43(2): 249–57. doi: 10.1016/j.burns.2016.08.013

  4. Mahdavian Delavary B, van der Veer WM, van Egmond M, Niessen FB, Beelen RH. Macrophages in skin injury and repair. Immunobiology 2011; 216(7): 753–62. doi: 10.1016/j.imbio.2011.01.001

  5. Chodorowska G, Rogus-Skorupska D. Cutaneous wound healing. Ann Univ Mariae Curie Sklodowska Med 2004; 59(2): 403–7.

  6. Razavi H, Darvishi MH, Janfaza S. Silver sulfadiazine encapsulated in lipid-based nanocarriers for burn treatment. J Burn Care Res 2018; 39(3): 319–25. doi: 10.1097/BCR.0000000000000602

  7. Hirsch T, Ashkar W, Schumacher O, Steinstraesser L, Ingianni G, Cedidi CC. Moist Exposed Burn Ointment (MEBO) in partial thickness burns – a randomized, comparative open mono-center study on the efficacy of dermaheal (MEBO) ointment on thermal 2nd degree burns compared to conventional therapy. Eur J Med Res 2008; 13(11): 505–10.

  8. Cheng YT, Wu SL, Ho CY, Huang SM, Cheng CL, Yen GC. Beneficial effects of Camellia Oil (Camellia oleifera Abel.) on ketoprofen-induced gastrointestinal mucosal damage through upregulation of HO-1 and VEGF. J Agric Food Chem 2014; 62(3): 642–50. doi: 10.1021/jf404614k

  9. Tu PS, Tung YT, Lee WT, Yen GC. Protective effect of Camellia Oil (Camellia oleifera Abel.) against ethanol-induced acute oxidative injury of the gastric mucosa in mice. J Agric Food Chem 2017; 65(24): 4932–41. doi: 10.1021/acs.jafc.7b01135

  10. Lee WT, Tung YT, Wu CC, Tu PS, Yen GC. Camellia Oil (Camellia oleifera Abel.) modifies the composition of gut microbiota and alleviates acetic acid-induced colitis in rats. J Agric Food Chem 2018; 66(28): 7384–92. doi: 10.1021/acs.jafc.8b02166

  11. Xiao X, He L, Chen Y, Wu L, Wang L, Liu Z. Anti-inflammatory and antioxidative effects of Camellia oleifera Abel components. Future Med Chem 2017; 9(17): 2069–79. doi: 10.4155/fmc-2017-0109

  12. Hu JL, Nie SP, Huang DF, Li C, Xie MY, Wan Y. Antimicrobial activity of saponin-rich fraction from Camellia oleifera cake and its effect on cell viability of mouse macrophage RAW 264.7. J Sci Food Agric 2012; 92(12): 2443–9. doi: 10.1002/jsfa.5650

  13. Ye Y, Xing H, Chen X. Anti-inflammatory and analgesic activities of the hydrolyzed sasanquasaponins from the defatted seeds of Camellia oleifera. Arch Pharm Res 2013; 36(8): 941–51. doi: 10.1007/s12272-013-0138-y

  14. Sekine T, Arita J, Yamaguchi A, Saito K, Okonogi S, Morisaki N, et al. Two flavonol glycosides from seeds of Camellia sinensis. Phytochemistry 1991; 30(3): 991–5.

  15. Lee HB, Kim EK, Park SJ, Bang SG, Kim TG, Chung DW. Isolation and anti-inflammatory effect of astragalin synthesized by enzymatic hydrolysis of tea seed extract. J Sci Food Agric 2011; 91(13): 2315–21. doi: 10.1002/jsfa.4457

  16. Robbins JB, Reinisch L, Ellis DL. Wound healing of 6.45-microm free electron laser skin incisions with heat-conducting templates. J Biomed Opt 2003; 8(4): 594–600. doi: 10.1117/1.1609452

  17. Altamirano J, Miquel R, Katoonizadeh A, Abraldes JG, Duarte-Rojo A, Louvet A, et al. A histologic scoring system for prognosis of patients with alcoholic hepatitis. Gastroenterology 2014; 146(5): 1231–9.e1–6. doi: 10.1053/j.gastro.2014.01.018

  18. Theunissen D, Seymour B, Forder M, Cox SG, Rode H. Measurements in wound healing with observations on the effects of topical agents on full thickness dermal incised wounds. Burns 2016; 42(3): 556–63. doi: 10.1016/j.burns.2015.09.014

  19. Landen NX, Li D, Stahle M. Transition from inflammation to proliferation: a critical step during wound healing. Cell Mol Life Sci 2016; 73(20): 3861–85. doi: 10.1007/s00018-016-2268-0

  20. Li YY, Xiao L, Qiu LY, Yan YF, Wang H, Duan GL, et al. Sasanquasaponin-induced cardioprotection involves inhibition of mPTP opening via attenuating intracellular chloride accumulation. Fitoterapia 2017; 116: 1–9. doi: 10.1016/j.fitote.2016.11.003

  21. Qiu LY, Duan GL, Yan YF, Li YY, Wang H, Xiao L, et al. Sasanquasaponin induces increase of Cl/HCO3 exchange of anion exchanger 3 and promotes intracellular Cl efflux in hypoxia/reoxygenation cardiomyocytes. Mol Med Rep 2017; 16(3): 2953–61. doi: 10.3892/mmr.2017.6882

  22. Ye Y, Xing H, Li Y. Nanoencapsulation of the sasanquasaponin from Camellia oleifera, its photo responsiveness and neuroprotective effects. Int J Nanomed 2014; 9: 4475–84. doi: 10.2147/IJN.S64313

  23. Zeng J, Chen S, Li N, Chen L, Su J, Niu G, et al. Sasanquasaponin from Camellia oleifera Abel. induces apoptosis via Bcl-2, Bax and caspase-3 activation in HepG2 cells. Mol Med Rep 2015; 12(2): 1997–2002. doi: 10.3892/mmr.2015.3666

  24. Chen L, Chen J, Xu H. Sasanquasaponin from Camellia oleifera Abel. induces cell cycle arrest and apoptosis in human breast cancer MCF-7 cells. Fitoterapia 2013; 84: 123–9. doi: 10.1016/j.fitote.2012.11.009

  25. Koh TJ, DiPietro LA. Inflammation and wound healing: the role of the macrophage. Expert Rev Mol Med 2011; 13: e23. doi: 10.1017/S1462399411001943

  26. Pastar I, Stojadinovic O, Yin NC, Ramirez H, Nusbaum AG, Sawaya A, et al. Epithelialization in wound healing: a comprehensive review. Adv Wound Care (New Rochelle) 2014; 3(7): 445–64. doi: 10.1089/wound.2013.0473

  27. Pakyari M, Farrokhi A, Maharlooei MK, Ghahary A. Critical role of transforming growth factor beta in different phases of wound healing. Adv Wound Care (New Rochelle) 2013; 2(5): 215–24. doi: 10.1089/wound.2012.0406

  28. Weber CE, Li NY, Wai PY, Kuo PC. Epithelial-mesenchymal transition, TGF-beta, and osteopontin in wound healing and tissue remodeling after injury. J Burn Care Res 2012; 33(3): 311–18. doi: 10.1097/BCR.0b013e318240541e

  29. Ganeshkumar M, Ponrasu T, Krithika R, Iyappan K, Gayathri VS, Suguna L. Topical application of Acalypha indica accelerates rat cutaneous wound healing by up-regulating the expression of Type I and III collagen. J Ethnopharmacol 2012; 142(1): 14–22. doi: 10.1016/j.jep.2012.04.005

  30. Aust MC, Knobloch K, Reimers K, Redeker J, Ipaktchi R, Altintas MA, et al. Percutaneous collagen induction therapy: an alternative treatment for burn scars. Burns 2010; 36(6): 836–43. doi: 10.1016/j.burns.2009.11.014

  31. Babaei S, Bayat M. Pentoxifylline accelerates wound healing process by modulating gene expression of MMP-1, MMP-3, and TIMP-1 in normoglycemic rats. J Invest Surg 2015; 28(4): 196–201. doi: 10.3109/08941939.2014.1002642

  32. Cai QW, Li J, Li XQ, Wang JQ, Huang Y. Expression of STAT3, MMP-1 and TIMP-1 in gastric cancer and correlation with pathological features. Mol Med Rep 2012; 5(6): 1438–42. doi: 10.3892/mmr.2012.849

Published
2020-03-06
How to Cite
Liu Y., Xiao X., Ji L., Xie L., Wu S., & Liu Z. (2020). <em>Camellia</em&gt; cake extracts reduce burn injury through suppressing inflammatory responses and enhancing collagen synthesis. Food & Nutrition Research, 64. https://doi.org/10.29219/fnr.v64.3782
Section
Original Articles