Dose-dependent effect of local treatment of Phyllanthus emblica L. cream on diabetic wound

Authors

  • Ting-ting Liao Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
  • Supakanda Sukpat Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
  • Chaisak Chansriniyom Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand
  • Suthiluk Patumraj Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand

Keywords:

Diabetic wound, Phyllanthus emblica Linn., wound closure, capillary vascularity

Abstract

Background: Non-healing diabetic ulcers are the most common cause of amputation. Several studies have reported for new, more effective treatments for chronic wounds in diabetic patients.

Objective: This study aimed to evaluate the effect of local treatment of Phyllanthus emblica Linn. (PE) on a full-thickness wound model in streptozotocin-induced diabetic mice.

Methods: Balb/c mice were divided into five groups: control group (CON), diabetic wounded group (DM, streptozotocin 45 mg/kg i.p. daily for 5 days), diabetic wounded group with daily treatment of different concentrations of PE cream (10%; 100%; and 200%, w/v). Seven days after the diabetic induction, all mice were created bilateral full-thickness excisional skin wounds on the back and received vehicle or PE cream into wound bed. At day 14 post-wounding, the percentage of wound closure (%WC) and the percentage of capillary vascularity (%CV) were determined by using confocal fluorescence microscopy and digital image analysis.

Results: The dose-dependent of PE on diabetic wounds were determined by both findings of %WC and %CV. The results showed positive correlation between various doses of topical PE and 14-day %CV post-wound creation (r = 0.7197) (P = 0.0017). The linear regression equation, Y = 0.01788X + 37.35, with R2 = 0.5180, described the relationship between PE doses and CV%.

Conclusion: These findings show that local administration of PE cream improved the healing process of diabetic wounds in associated with PE’s angiogenic effect in a dose-dependent manner.

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References

Ogurtsova K, da Rocha Fernandes JD, Huang Y, Linnenkamp U, Guariguata L, Cho NH, et al. IDF diabetes atlas: global estimates for the prevalence of diabetes for 2015 and 2040. Diabetes Res Clin Pract 2017;128:40-50.

https://doi.org/10.1016/j.diabres.2017.03.024

Schreiber J, Efron PA, Park JE, Moldawer LL, Barbul A. Adenoviral gene transfer of an NF-kappaB superrepressor increases collagen deposition in rodent cutaneous wound healing. Surgery 2005;138:940-6.

https://doi.org/10.1016/j.surg.2005.05.020

Pecoraro RE, Reiber GE, Burgess EM. Pathways to diabetic limb amputation. Basis for prevention. Diabetes Care 1990;13:513-21.

https://doi.org/10.2337/diacare.13.5.513

Sukpat S, Israsena N, Patumraj S. Pleiotropic effects of simvastatin on wound healing in diabetic mice. J Med Assoc Thai 2016;99:213-9.

Asai J, Takenaka H, Hirakawa S, Sakabe J, Hagura A, Kishimoto S, et al. Topical simvastatin accelerates wound healing in diabetes by enhancing angiogenesis and lymphangiogenesis. Am J Pathol 2012;181:2217-24. https://doi.org/10.1016/j.ajpath.2012.08.023

Unander DW, Webster GL, Blumberg BS. Usage and bioassays in Phyllanthus (Euphorbiaceae). IV. Clustering of antiviral uses and other effects. J Ethnopharmacol 1995;45:1-18. https://doi.org/10.1016/0378-8741(94)01189-7

Unander DW, Webster GL, Blumberg BS. Records of usage or assays in Phyllanthus (Euphorbiaceae).I. Subgenera Isocladus, Kirganelia, Cicca and Emblica. J Ethnopharmacol 1990;30:233-64. https://doi.org/10.1016/0378-8741(90)90105-3

Kirtikar KR, Basu BD. In: Kirtikar KR, Basu BD, editors. Indian medicinal plants, 2nd ed. Allahabad: Lolit Mohan Basu Publication;1935. p.1020-23.

Krishnaveni M, Mirunalini S, Karthishwaran K, Dhamodharan G. Antidiabetic and antihyperlipidemic properties of Phyllanthus emblica Linn. (Euphorbiaceae) on streptozotocin induced diabetic rats. Pak J Nutr 2010;9:43-51.

https://doi.org/10.3923/pjn.2010.43.51

Sukpat S, Isarasena N, Wongphoom J, Patumraj S. Vasculoprotective effects of combined endothelial progenitor cells and mesenchymal stem cells in diabetic wound care: their potential role in decreasing wound-oxidative stress. Biomed Res Int 2013:459196. https://doi.org/10.1155/2013/459196

Wu Y, Chen L, Scott PG, Tredget EE. Mesenchymal stem cells enhance wound healing through differentiation and angiogenesis. Stem Cells 2007;25:2648-59. https://doi.org/10.1634/stemcells.2007-0226

Sivan-Loukianova E, Awad OA, Stepanovic V, Bickenbach J, Schatteman GC. CD34+ blood cells accelerate vascularization and healing of diabetic mouse skin wounds. J Vasc Res 2003;40:368-77. https://doi.org/10.1159/000072701

Chokesuwattanaskul S, Sukpat S, Duangpatra J, Buppajarntham S, Decharatanachart P, Mutirangura A, Patumraj S. High dose oral vitamin C and mesenchymal stem cells aid wound healing in a diabetic mouse model. J Wound Care 2018;27:334-9.

https://doi.org/10.12968/jowc.2018.27.5.334

Saraheimo M, Teppo AM, Forsblom C, Fagerudd J, Groop PH. Diabetic nephropathy is associated with low-grade inflammation in Type 1 diabetic patients. Diabetologia 2003;46:1402-7. https://doi.org/10.1007/s00125-003-1194-5

Garcia C, Feve B, Ferre P, Halimi S, Baizri H, Bordier L, et al. Diabetes and inflammation: fundamental aspects and clinical implications. Diabetes Metab 2010;36:327-38. https://doi.org/10.1016/j.diabet.2010.07.001

Boakye YD, Agyare C, Ayande GP, Titiloye N, Asiamah EA, Danquah KO. Assessment of woundhealing properties of medicinal plants: The case of Phyllanthus muellerianus. Front Pharmacol 2018;9:945. https://doi.org/10.3389/fphar.2018.00945

Suguna L, Singh S, Sivakumar P, Sampath P, Chandrakasan G. Influence of Terminalia chebulaon on dermal wound healing in rats. Phytother Res 2002;16:227-31. https://doi.org/10.1002/ptr.827

Tang T, Yin L, Yang J, Shan G. Emodin, an anthraquinone derivative from Rheum officinale Baill, enhances cutaneous wound healing in rats. Eur J Pharmacol 2007;567: 177-85. https://doi.org/10.1016/j.ejphar.2007.02.033

Singh E, Sharma S, Pareek A, Dwivedi J, Yadav S, Sharma S. Phytochemistry, traditional uses and cancer chemopreventive activity of Amla (Phyllanthus emblica): The Sustainer. J Appl Pharm Sci 2011;2:176-83.

Yadav SS, Singh MK, Singh PK, Kumar V. Traditional knowledge to clinical trials: a review on therapeutic actions of Emblica officinalis. Biomed Pharmacother 2017;93:1292-302. https://doi.org/10.1016/j.biopha.2017.07.065

Usharani P, Fatima N, Muralidhar N. Effects of Phyllanthus emblica extract on endothelial dysfunction and biomarkers of oxidative stress in patients with type 2 diabetes mellitus: a randomized, double-blind, controlled study. Diabetes Metab Syndr Obes 2013;6:275-84. https://doi.org/10.2147/DMSO.S46341

Chansriniyom C, Bunwatcharaphansakun P, Eaknai W, Nalinratana N, Ratanawong A, Khongkow M, et al. A synergistic combination of Phyllanthus emblica and Alpinia galanga against H2O2-induced oxidative stress and lipid peroxidation in human ECV304 cells. J Funct Foods 2018;43:44-54. https://doi.org/10.1016/j.jff.2018.01.016

Usharani P, Kishan PV, Fatima N, Kumar CU. A comparative study to evaluate the effect of highly standardised aqueous extracts of Phyllanthus emblica, Withania somnifera and their combination on endothelial dysfunction and biomarkers in patients with type 2 diabetes mellitus. Int J Pharm Sci Res 2014;5:2687-97.

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Published

2023-07-17

How to Cite

1.
Liao T- ting, Sukpat S, Chansriniyom C, Patumraj S. Dose-dependent effect of local treatment of Phyllanthus emblica L. cream on diabetic wound. Chula Med J [Internet]. 2023 Jul. 17 [cited 2024 May 20];66(2). Available from: https://he05.tci-thaijo.org/index.php/CMJ/article/view/65