Topical administration of mangiferin promotes healing of the wound of streptozotocin-nicotinamide-induced type-2 diabetic male rats

References

• Reinke JM, Sorg H. Wound repair and regeneration. Eur Surg Res. 2012;49(1):35–43.
   PubMed Web of Science ®Google Scholar
• Zhao R, Liang H, Clarke E, et al. Inflammation in chronic wounds. Int J Mol Sci. 2016;17(12):2085.
   PubMed Web of Science ®Google Scholar
• Frykberg RG, Banks J. Challenges in the treatment of chronic wounds. Adv Wound Care. 2015;4(9):560–582.
   PubMed Web of Science ®Google Scholar
• Serra MB, Barroso WA, da Silva NN, et al. From inflammation to current and alternative therapies involved in wound healing. Int J Inflam. 2017;2017:1–17.
   Web of Science ®Google Scholar
• Velnar T, Bailey T, Smrkolj V. The wound healing process: an overview of the cellular and molecular mechanisms. J Int Med Res. 2009;37(5):1528–1542.
   PubMed Web of Science ®Google Scholar
• Mudge E, Price P, Walkley N, et al. A randomized controlled trial of larval therapy for the debridement of leg ulcers: results of a multicenter, randomized, controlled, open, observer blind, parallel group study. Wound Repair Regen. 2014;22(1):43–51.
   PubMed Web of Science ®Google Scholar
• Elgharably H, Roy S, Khanna S, et al. A modified collagen gel enhances healing outcome in a pre-clinical swine model of excisional wounds. Wound Repair Regen. 2013;21(3):473–481.
   PubMed Web of Science ®Google Scholar
• Liu WY, Tzeng TF, Liu IM. Healing potential of zerumbone ointment on experimental full-thickness excision cutaneous wounds in rat. J Tissue Viability. 2017;26(3):202–207.
   PubMed Web of Science ®Google Scholar
• Ram M, Singh V, Kumawat S, et al. Bilirubin modulated cytokines, growth factors and angiogenesis to improve cutaneous wound healing process in diabetic rats. Int Immunopharmacol. 2016;30:137–149.
   PubMed Web of Science ®Google Scholar
• Kant V, Gopal A, Kumar D, et al. Curcumin-induced angiogenesis hastens wound healing in diabetic rats. J Surg Res. 2015;193(2):978–988.
   PubMed Web of Science ®Google Scholar
• Shah KA, Patel MB, Patel RJ, et al. Mangifera indica (Mango). Phcog Rev. 2010;4(7):42–48.
   Google Scholar
• Du S, Liu H, Lei T, et al. Mangiferin: an effective therapeutic agent against several disorders (Review). Mol Med Report. 2018;18(6):4775–4786.
   PubMed Web of Science ®Google Scholar
• Alberdi E, Sanchez-Gomez MV, Ruiz A, et al. Mangiferin and morin attenuate oxidative stress, mitochondrial dysfunction, and neurocytotoxicity, induced by amyloid beta oligomers. Oxid Med Cell Longev. 2018;2018:1–13.
   Web of Science ®Google Scholar
• Jyotshna , Khare P, Shanker K. Mangiferin: a review of sources and interventions for biological activities. BioFactors. 2016;42(5):504–514.
   PubMed Web of Science ®Google Scholar
• Pal PB, Sinha K, Sil PC. Mangiferin, a natural xanthone, protects murine liver in Pb(II) induced hepatic damage and cell death via MAP kinase, NF-kappaB and mitochondria dependent pathways. PloS One. 2013;8(2):e56894.
   PubMed Web of Science ®Google Scholar
• Bulugonda RK, Kumar KA, Gangappa D, et al. Mangiferin from Pueraria tuberosa reduces inflammation via inactivation of NLRP3 inflammasome. Sci Rep. 2017;7(1):42683.
   PubMedGoogle Scholar
• Bamidele O, Kolawole J, Ayoka A, et al. Wound healing potentials of aqueous leaf extract of Mangifera indica L. in Wistar Rats. J Complement Altern Med Res. 2016;
   Google Scholar
• Nuevo JJM, Bernardino E. The effect of Mangifera indica (Mango) leaf crude extract in the wound healing properties of Rattus norvegicus (Sprague Dawley). Fatima Univ Res J. 2013;5(1):1–1.
   Google Scholar
• Giribabu N, Karim K, Kilari EK, et al. Anti-inflammatory, antiapoptotic and proproliferative effects of Vitis vinifera seed ethanolic extract in the liver of streptozotocin-nicotinamide-induced type 2 diabetes in male rats. Can J Diabetes. 2018;42(2):138–149.
   PubMed Web of Science ®Google Scholar
• Tan NAS, Giribabu N, Karim K, et al. Intravaginal treatment with Marantodes pumilum (Kacip Fatimah) ameliorates vaginal atrophy in rats with post-menopausal condition. J Ethnopharmacol. 2019;236:9–20.
   PubMed Web of Science ®Google Scholar
• Loh SY, Giribabu N, Salleh N. Sub-chronic testosterone treatment increases the levels of epithelial sodium channel (ENaC)-α, β and γ in the kidney of orchidectomized adult male Sprague–Dawley rats. PeerJ. 2016;4:e2145.
   PubMed Web of Science ®Google Scholar
• Shahzad H, Giribabu N, Karim K, et al. Combinatorial effects of quercetin and sex-steroids on fluid and electrolytes’ (Na+, Cl−, HCO3−) secretory mechanisms in the uterus of ovariectomised female Sprague-Dawley rats. PLoS One. 2017;12(3):e0172765.
   PubMed Web of Science ®Google Scholar
• Giribabu N, Karim K, Kilari EK, et al. Phyllanthus niruri leaves aqueous extract improves kidney functions, ameliorates kidney oxidative stress, inflammation, fibrosis and apoptosis and enhances kidney cell proliferation in adult male rats with diabetes mellitus. J Ethnopharmacol. 2017;205:123–137.
   PubMed Web of Science ®Google Scholar
• Giribabu N, Karim K, Salleh N. Effects of Marantodes pumilum (Kacip Fatimah) on vaginal pH and expression of vacoular ATPase and carbonic anhydrase in the vagina of sex-steroid deficient female rats. Phytomedicine. 2018;49:95–105.
   PubMed Web of Science ®Google Scholar
• Okonkwo UA, DiPietro LA. Diabetes and wound angiogenesis. Int J Mol Sci. 2017;18(7):1419.
   PubMed Web of Science ®Google Scholar
• Jeong L, Kim MH, Jung J-Y, et al. Effect of silk fibroin nanofibers containing silver sulfadiazine on wound healing. Int J Nanomedicine. 2014;9:5277–5287.
   PubMed Web of Science ®Google Scholar
• Sellamuthu PS, Arulselvan P, Kamalraj S, et al. Protective nature of mangiferin on oxidative stress and antioxidant status in tissues of streptozotocin-induced diabetic rats. ISRN Pharmacology. 2013;2013:1–10.
   Google Scholar
• Busik JV, Mohr S, Grant MB. Hyperglycemia-induced reactive oxygen species toxicity to endothelial cells is dependent on paracrine mediators. Diabetes. 2008;57(7):1952–1965.
   PubMed Web of Science ®Google Scholar
• Han G, Ceilley R. Chronic wound healing: a review of current management and treatments. Adv Ther. 2017;34(3):599–610.
   PubMed Web of Science ®Google Scholar
• Eming SA, Martin P, Tomic-Canic M. Wound repair and regeneration: mechanisms, signaling, and translation. Sci Transl Med. 2014;6(265):265sr6–265sr6.
   PubMed Web of Science ®Google Scholar
• Bodnar RJ. Epidermal growth factor and epidermal growth factor receptor: the yin and yang in the treatment of cutaneous wounds and cancer. Adv Wound Care. 2013;2(1):24–29.
   Google Scholar
• Xu K, Yu FS. Impaired epithelial wound healing and EGFR signaling pathways in the corneas of diabetic rats. Invest Ophthalmol Vis Sci. 2011;52(6):3301–3308.
   PubMed Web of Science ®Google Scholar
• Portero-Otin M, Pamplona R, Bellmunt MJ, et al. Advanced glycation end product precursors impair epidermal growth factor receptor signaling. Diabetes. 2002;51(5):1535–1542.
   PubMed Web of Science ®Google Scholar
• Demidova-Rice TN, Hamblin MR, Herman IM. Acute and impaired wound healing: pathophysiology and current methods for drug delivery, Part 2: role of growth factors in normal and pathological wound healing: therapeutic potential and methods of delivery. Adv Skin Wound Care. 2012;25(8):349–370.
   PubMed Web of Science ®Google Scholar
• Barrientos S, Brem H, Stojadinovic O, et al. Clinical application of growth factors and cytokines in wound healing. Wound Repair Regen. 2014;22(5):569–578.
   PubMed Web of Science ®Google Scholar
• Matsumoto S, Tanaka R, Okada K, et al. The effect of control-released basic fibroblast growth factor in wound healing: histological analyses and clinical application. Plastic Reconstr Surg Glob Open. 2013;1(6):e44.
   Google Scholar
• Uchi H, Igarashi A, Urabe K, et al. Clinical efficacy of basic fibroblast growth factor (bFGF) for diabetic ulcer. Eur J Dermatol. 2009;19(5):461–468.
   PubMed Web of Science ®Google Scholar
• Shah JM, Omar E, Pai DR, et al. Cellular events and biomarkers of wound healing. Indian J Plast Surg. 2012;45(2):220–228.
   PubMedGoogle Scholar
• Lichtman MK, Otero-Vinas M, Falanga V. Transforming growth factor beta (TGF-beta) isoforms in wound healing and fibrosis. Wound Rep and Reg. 2016;24(2):215–222.
   PubMed Web of Science ®Google Scholar
• Pakyari M, Farrokhi A, Maharlooei MK, et al. Critical role of transforming growth factor beta in different phases of wound healing. Adv Wound Care. 2013;2(5):215–224.
   PubMedGoogle Scholar
• Johnson KE, Wilgus TA. Vascular endothelial growth factor and angiogenesis in the regulation of cutaneous wound repair. Adv Wound Care. 2014;3(10):647–661.
   PubMedGoogle Scholar
• Bao P, Kodra A, Tomic-Canic M, et al. The role of vascular endothelial growth factor in wound healing. J Surg Res. 2009;153(2):347–358.
   PubMed Web of Science ®Google Scholar
• Zhang E, Gao B, Yang L, et al. Notoginsenoside Ft1 promotes fibroblast proliferation via PI3K/Akt/mTOR signaling pathway and benefits wound healing in genetically diabetic mice. J Pharmacol Exp Ther. 2016;356(2):324–332.
   PubMed Web of Science ®Google Scholar
• Lawrence T. The nuclear factor NF-κB pathway in inflammation. Cold Spring Harb Perspect Biol. 2009;1(6):a001651–a001651.
   PubMed Web of Science ®Google Scholar
• Verrecchia F, Mauviel A. Transforming growth factor-β and fibrosis. World J Gastroenterol. 2007;13(22):3056–3062.
   PubMed Web of Science ®Google Scholar
• Eming SA, Krieg T, Davidson JM. Inflammation in wound repair: molecular and cellular mechanisms. J Invest Dermatol. 2007;127(3):514–525.
   PubMed Web of Science ®Google Scholar
• Negrean M, Stirban A, Stratmann B, et al. Effects of low-and high-advanced glycation endproduct meals on macro-and microvascular endothelial function and oxidative stress in patients with type 2 diabetes mellitus. Am J Clin Nutr. 2007;85(5):1236–1243.
   PubMed Web of Science ®Google Scholar
• Xue M, Jackson CJ. Extracellular matrix reorganization during wound healing and its impact on abnormal scarring. Adv Wound Care. 2015;4(3):119–136.
   PubMed Web of Science ®Google Scholar
• Ayuk SM, Abrahamse H, Houreld NN. The role of matrix metalloproteinases in diabetic wound healing in relation to photobiomodulation. J Diabetes Res. 2016;2016:1–9.
   Web of Science ®Google Scholar
• Caley MP, Martins VL, EAJAiwc O. Metalloproteinases and wound healing. Adv Wound Care. 2015;4(4):225–234.
   PubMed Web of Science ®Google Scholar
• Ahmed SMU, Luo L, Namani A, et al. Nrf2 signaling pathway: pivotal roles in inflammation. Biochim Biophys Acta Mol Basis Dis. 2017;1863(2):585–597.
   PubMed Web of Science ®Google Scholar
• Long M, De La Vega MR, Wen Q, et al. An essential role of NRF2 in diabetic wound healing. Diabetes. 2016;65(3):780–793.
   PubMed Web of Science ®Google Scholar
• Jindam A, Yerra VG, Kumar A. Nrf2: a promising trove for diabetic wound healing. Ann Transl Med. 2017;5(23):469–469.
   PubMed Web of Science ®Google Scholar