MENTHA SPİCATA UÇUCU YAĞ EKSTRESİNİN İÇERİK ANALİZİYLE, SIÇANLARDA YARA İYİLEŞMESİNE ETKİSİNİN İNCELENMESİ
Year 2023,
Volume: 10 Issue: 4, 134 - 143, 15.06.2023
Melek Atille
,
Ela Tules Kadiroğlu
,
Abdulselam Ertaş
,
Berna Ersöz Kanay
,
Nezahat Akpolat
,
Engin Deveci
,
Fırat Aşır
Abstract
Amaç: Bu çalışmadaki amacımız Mentha spicata (MS) türünün uçucu yağ ekstresinin kimyasal ve antioksidan kompozisyonunu, bu bitkiye ait ekstrenin antibakteriyel aktivitesini ve sıçan damak bölgesinde yara iyileşmesi üzerindeki etkinliğini değerlendirmektir.
Yöntem ve gereçler: MS ekstresinin antioksidan aktivitesi DPPH serbest radikal giderim, ABTS katyon radikal giderim ve CUPRAC yöntemleri ile tayin edildi. Ayrıca türün antiaging poptansiyeli elastaz ve kollajenaz enzim aktiviteleri ile belirlenerek uçucu yağ içeriği GC-MS/FID ile analiz edildi. Yara iyileşmesindeki etkinliğin değerlendirilmesi amacıyla da 8-10 haftalık, 56 adet Wistar albino türü erkek ratın damağında 4 mm çapında eksizyonal yara bölgesi oluşturuldu. Denekler; kontrol grubu (K), ve Mentha spicata (MS) grubu şeklinde 2 eşit gruba bölündü ve 3, 7, 14 ve 21.günlerde sakrifiye edildi. Yara bölgelerinden histopatolojik inceleme için doku örnekleri alındı. Histopatolojik olarak; vaskülarizasyon, polimorfonükleer lökosit (PMN) sayısı, kollajen dejenerasyonu, fibrozis, vasküler endotelyal büyüme faktörü (VEGF) ve vimentin parametreleri değerlendirildi. Antimikrobiyal etkinliğin saptanmasında ise Streptococcus mitis (S. mitis) ve Aggregatibacter actinomycetemcomitans (Aa) bakterileri kullanıldı.
Bulgular: Antioksidan değerlendirmede; daha çok monoterpenlerden oluşan MS uçucu yağ ekstresi orta derecede aktif bulundu. Yara iyileşmesindeki istatistiksel analiz sonuçlarına göre ise; MS grubu, kontrol grubu ile karşılaştırıldığında, 14 ve 21.günlerde anlamlı olarak azalmış vaskülarizasyon, PMN, kollajen dejenerasyonu, fibrozis ve vimentin değerleri görülürken; aynı günlerde VEGF değerleri anlamlı olarak fazla bulundu. MS’nin S. mitis ve Aa bakterileri bir antibakteriyel etkisi tespit edilmedi.
Sonuç: Mentha spicata’nın ise ağız içi yara iyileşmesinde orta derecede etkili olduğu görüldü.
Anahtar kelimeler: Antibakteriyel, Antioksidan, Kloroben, Mentha Spicata, Yara İyileşmesi
Supporting Institution
Dicle Üniversitesi Bilimsel Araştırma Projeleri Birimi
References
- 1. Dieni da Silveira Teixeira 1, Maria Antonia Zancanaro de Figueiredo, Karen Cherubini, Sílvia Dias de Oliveira FGS. The topical effect of chlorhexidine and povidone-iodine in the repair of oral wounds. A review. Balt Dent Maxillofac J. 2019;21(2):35–41.
- 2. Kozlovsky A, Artzi Z, Hirshberg A, Israeli-Tobias C, Reich L. Effect of local antimicrobial agents on excisional palatal wound healing: A clinical and histomorphometric study in rats. J Clin Periodontol. 2007 Feb;34(2):164–71.
- 3. Kovalik AC, Bisetto P, Pochapski MT, Campagnoli EB, Pilatti GL, Santos FA. Effects of an orabase formulation with ethanolic extract of malva sylvestris L. in oral wound healing in rats. J Med Food. 2014 May 1;17(5):618–24.
- 4. Moghadam ET, Yazdanian M, Tahmasebi E, Tebyanian H, Ranjbar R, Yazdanian A, et al. Current herbal medicine as an alternative treatment in dentistry: In vitro, in vivo and clinical studies. Vol. 889, European Journal of Pharmacology. Elsevier B.V.; 2020.
- 5. Verma Sheetal, Singh S.P. Current and Future Status of Herbal Medicines. Vet World. 2008 Nov;1(11):347–50.
- 6. Strauss SE. Evidence-Based Herbal Medicine. Evid Based Med. 2003 Jan 1;8(1):8–8.
- 7. Conway GA, Slocumb JC. Plants used as abortifacients and emmenagogues by Spanish New Mexicans. J Ethnopharmacol. 1979;1(3):241–61.
- 8. Mahboubi M. Mentha spicata as natural analgesia for treatment of pain in osteoarthritis patients. Vol. 26, Complementary Therapies in Clinical Practice. Churchill Livingstone; 2017. p. 1–4.
- 9. Ali-Shtayeh MS, Jamous RM, Abu-Zaitoun SY, Khasati AI, Kalbouneh SR. Biological Properties and Bioactive Components of Mentha spicata L. Essential Oil: Focus on Potential Benefits in the Treatment of Obesity, Alzheimer’s Disease, Dermatophytosis, and Drug-Resistant Infections. Evidence-based Complement Altern Med. 2019;2019.
- 10. Direito R, Rocha J, Lima A, Gonçalves MM, Duarte MP, Mateus V, et al. Reduction of Inflammation and Colon Injury by a Spearmint Phenolic Extract in Experimental Bowel Disease in Mice. Medicines. 2019;6(2):65.
- 11. Arumugam P, Priya NG, Subathra M, Ramesh A. Anti-inflammatory activity of four solvent fractions of ethanol extract of Mentha spicata L . investigated on acute and chronic inflammation induced rats. 2008;26:92–5.
- 12. Mariano RC, Oliveira MR, Silva LC, Ferreira S, Garcia Júnior IR, De Carvalho Silva A. Effect of topical application of chlorhexidine and metronidazole on the tissue repair of palatal wounds of rats: A clinical and histomorphometric study. Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 May 1;119(5):505–13.
- 13. Kim YJ, Carvalho FC, Souza JAC, Gonçalves PCG, Nogueira AVB, Spolidõrio LC, et al. Topical application of the lectin Artin M accelerates wound healing in rat oral mucosa by enhancing TGF-β and VEGF production. Wound Repair Regen. 2013 May;21(3):456–63.
- 14. Trindade LC, Biondo-Simões Mde L, Sampaio CP, Farias RE, Pierin RJ, Netto MC. Evaluation of topical metronidazole in the healing wounds process: an experimental study. Rev Col Bras Cir. 2010 Oct;37(5):358-63. English, Portuguese. doi: 10.1590/s0100-69912010000500009. PMID: 21181002.
- 15. Hacettepe Üniversitesi Tıp Fakültesi D, Mikrobiyoloji Anabilim Dalı T. Türk Mikrobiyoloji Cemiyeti Dergisi- Journal Of Turkısh Socıety Of Mıcrobıology Antibiyotik Duyarlılık Testleri, EUCAST: Uygulama, Yorum ve Uzman Kurallar Editör. 1993;
- 16. Balouiri M, Sadiki M, Ibnsouda SK. Methods for in vitro evaluating antimicrobial activity: A review. J Pharm Anal. 2016;6(2):71–9.
- 17. Godbole GB, Modi DN, Puri CP. Regulation of homeobox A10 expression in the primate endometrium by progesterone and embryonic stimuli. 2005;
- 18. Islam B, Khan SN, Khan AU. Dental caries: from infection to prevention. Med Sci Monit. 2007 Nov;13(11):RA196-203.
- 19. Gürgan CA, Zaim E, Bakirsoy I, Soykan E. Short-Term Side Effects of 0.2% Alcohol-Free Chlorhexidine Mouthrinse Used as an Adjunct to Non-Surgical Periodontal Treatment: A Double-Blind Clinical Study. J Periodontol. 2006 Mar;77(3):370–84.
- 20. Guo S, DiPietro LA. Critical review in oral biology & medicine: Factors affecting wound healing. J Dent Res. 2010 Mar;89(3):219–29.
- 21. Bao P, Kodra A, Tomic-Canic M, Golinko MS, Ehrlich HP, Brem H. The Role of Vascular Endothelial Growth Factor in Wound Healing. J Surg Res. 2009;153(2):347–58.
- 22. Gantwerker EA, Hom DB. Skin: Histology and Physiology of Wound Healing. Vol. 19, Facial Plastic Surgery Clinics of North America. 2011. p. 441–53.
- 23. Banaudha KK, Patnaik GK, Maheshwari RK. Curcumin enhances wound healing in streptozotocin induced diabetic rats and genetically diabetic mice. 1999;
- 24. Ross R, Bendıtt EP. Wound healing and collagen formation. I. Sequential changes in components of guinea pig skin wounds observed in the electron microscope. J Biophys Biochem Cytol. 1961;11:677–700.
- 25. Ross R. The fibroblast and wound repair. Biol Rev Camb Philos Soc. 1968;43(1):51–96.
- 26. Gülpak M. Deneysel Diyabet Modeli Oluşturulmuş Ratlarda Lavanta Yağının Yara İyileşmesine Etkisi. Doktora Tezi, Gazi Üniversitesi 2020
- 27. Menke NB, Ward KR, Witten TM, Bonchev DG, Diegelmann RF. Impaired wound healing. Clin Dermatol. 2007;25(1):19–25.
- 28. Mogosan C, Vostinaru O, Oprean R, Heghes C, Filip L, Balica G, et al. A comparative analysis of the chemical composition, anti-inflammatory, and antinociceptive effects of the essential oils from three species of Mentha cultivated in Romania. Molecules. 2017 Feb 1;22(2).
- 29. Atiyah AG. The role of Helianthus tuberosus powder in healing of full-thickness wounds in mice. 2021;14:1290–8.
- 30. Mathew-Steiner SS, Roy S, Sen CK. Collagen in wound healing. Bioengineering. 2021;8(5).
- 31. Fazil M, Nikhat S. Topical medicines for wound healing: A systematic review of Unani literature with recent advances. J Ethnopharmacol. 2020;257(April):112878.
- 32. Frank S, Hubner G, Breier G, Longaker MT, Greenhalgh DG, Werner S. Regulation of vascular endothelial growth factor expression in cultured keratinocytes. Implications for normal and impaired wound healing. Vol. 270, Journal of Biological Chemistry. 1995. p. 12607–13.
- 33. Shukla A, Dubey MP, Srivastava R, Srivastava BS. Differential expression of proteins during healing of cutaneous wounds in experimental normal and chronic models. Biochem Biophys Res Commun. 1998;244(2):434–9.
- 34. Brown LF, Yeo KT, Berse B, Yeo TK, Senger DR, Dvorak HF, et al. Expression of vascular permeability factor (vascular endothelial growth factor) by epidermal keratinocytes during wound Healing. J Exp Med. 1992;176(5):1375–9.
- 35. Zhang Z, Wang S, Diao Y, Zhang J, Lv D. Fatty acid extracts from Lucilia sericata larvae promote murine cutaneous wound healing by angiogenic activity. 2010;1–9.
- 36. Cibrian D, Fuente H De, Sánchez-madrid F. Metabolic Pathways That Control Skin Homeostasis and Inflammation. Trends Mol Med. 2020;1–12.
- 37. Antfolk D, Sjöqvist M, Cheng F, Isoniemi K, Duran CL, Rivero-Muller A, et al. Selective regulation of Notch ligands during angiogenesis is mediated by vimentin. Proc Natl Acad Sci U S A. 2017;114(23):E4574–81.
- 38. Kartenbeck J, Schwechheimer K, Moll R, Franke WW. Attachment of vimentin filaments to desmosomal plaques in human meningiomal cells and arachnoidal tissue. J Cell Biol. 1984;98(3):1072–81.
- 39. Franke WW, Moll R. Cytoskeletal components of lymphoid organs. Differentiation. 1987;36(2):145–63.
- 40. Battaglia RA, Delic S, Herrmann H, Snider NT. Vimentin on the move: New developments in cell migration [version 1; referees: 2 approved]. F1000Research. 2018;7(0):1–10.
Year 2023,
Volume: 10 Issue: 4, 134 - 143, 15.06.2023
Melek Atille
,
Ela Tules Kadiroğlu
,
Abdulselam Ertaş
,
Berna Ersöz Kanay
,
Nezahat Akpolat
,
Engin Deveci
,
Fırat Aşır
References
- 1. Dieni da Silveira Teixeira 1, Maria Antonia Zancanaro de Figueiredo, Karen Cherubini, Sílvia Dias de Oliveira FGS. The topical effect of chlorhexidine and povidone-iodine in the repair of oral wounds. A review. Balt Dent Maxillofac J. 2019;21(2):35–41.
- 2. Kozlovsky A, Artzi Z, Hirshberg A, Israeli-Tobias C, Reich L. Effect of local antimicrobial agents on excisional palatal wound healing: A clinical and histomorphometric study in rats. J Clin Periodontol. 2007 Feb;34(2):164–71.
- 3. Kovalik AC, Bisetto P, Pochapski MT, Campagnoli EB, Pilatti GL, Santos FA. Effects of an orabase formulation with ethanolic extract of malva sylvestris L. in oral wound healing in rats. J Med Food. 2014 May 1;17(5):618–24.
- 4. Moghadam ET, Yazdanian M, Tahmasebi E, Tebyanian H, Ranjbar R, Yazdanian A, et al. Current herbal medicine as an alternative treatment in dentistry: In vitro, in vivo and clinical studies. Vol. 889, European Journal of Pharmacology. Elsevier B.V.; 2020.
- 5. Verma Sheetal, Singh S.P. Current and Future Status of Herbal Medicines. Vet World. 2008 Nov;1(11):347–50.
- 6. Strauss SE. Evidence-Based Herbal Medicine. Evid Based Med. 2003 Jan 1;8(1):8–8.
- 7. Conway GA, Slocumb JC. Plants used as abortifacients and emmenagogues by Spanish New Mexicans. J Ethnopharmacol. 1979;1(3):241–61.
- 8. Mahboubi M. Mentha spicata as natural analgesia for treatment of pain in osteoarthritis patients. Vol. 26, Complementary Therapies in Clinical Practice. Churchill Livingstone; 2017. p. 1–4.
- 9. Ali-Shtayeh MS, Jamous RM, Abu-Zaitoun SY, Khasati AI, Kalbouneh SR. Biological Properties and Bioactive Components of Mentha spicata L. Essential Oil: Focus on Potential Benefits in the Treatment of Obesity, Alzheimer’s Disease, Dermatophytosis, and Drug-Resistant Infections. Evidence-based Complement Altern Med. 2019;2019.
- 10. Direito R, Rocha J, Lima A, Gonçalves MM, Duarte MP, Mateus V, et al. Reduction of Inflammation and Colon Injury by a Spearmint Phenolic Extract in Experimental Bowel Disease in Mice. Medicines. 2019;6(2):65.
- 11. Arumugam P, Priya NG, Subathra M, Ramesh A. Anti-inflammatory activity of four solvent fractions of ethanol extract of Mentha spicata L . investigated on acute and chronic inflammation induced rats. 2008;26:92–5.
- 12. Mariano RC, Oliveira MR, Silva LC, Ferreira S, Garcia Júnior IR, De Carvalho Silva A. Effect of topical application of chlorhexidine and metronidazole on the tissue repair of palatal wounds of rats: A clinical and histomorphometric study. Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 May 1;119(5):505–13.
- 13. Kim YJ, Carvalho FC, Souza JAC, Gonçalves PCG, Nogueira AVB, Spolidõrio LC, et al. Topical application of the lectin Artin M accelerates wound healing in rat oral mucosa by enhancing TGF-β and VEGF production. Wound Repair Regen. 2013 May;21(3):456–63.
- 14. Trindade LC, Biondo-Simões Mde L, Sampaio CP, Farias RE, Pierin RJ, Netto MC. Evaluation of topical metronidazole in the healing wounds process: an experimental study. Rev Col Bras Cir. 2010 Oct;37(5):358-63. English, Portuguese. doi: 10.1590/s0100-69912010000500009. PMID: 21181002.
- 15. Hacettepe Üniversitesi Tıp Fakültesi D, Mikrobiyoloji Anabilim Dalı T. Türk Mikrobiyoloji Cemiyeti Dergisi- Journal Of Turkısh Socıety Of Mıcrobıology Antibiyotik Duyarlılık Testleri, EUCAST: Uygulama, Yorum ve Uzman Kurallar Editör. 1993;
- 16. Balouiri M, Sadiki M, Ibnsouda SK. Methods for in vitro evaluating antimicrobial activity: A review. J Pharm Anal. 2016;6(2):71–9.
- 17. Godbole GB, Modi DN, Puri CP. Regulation of homeobox A10 expression in the primate endometrium by progesterone and embryonic stimuli. 2005;
- 18. Islam B, Khan SN, Khan AU. Dental caries: from infection to prevention. Med Sci Monit. 2007 Nov;13(11):RA196-203.
- 19. Gürgan CA, Zaim E, Bakirsoy I, Soykan E. Short-Term Side Effects of 0.2% Alcohol-Free Chlorhexidine Mouthrinse Used as an Adjunct to Non-Surgical Periodontal Treatment: A Double-Blind Clinical Study. J Periodontol. 2006 Mar;77(3):370–84.
- 20. Guo S, DiPietro LA. Critical review in oral biology & medicine: Factors affecting wound healing. J Dent Res. 2010 Mar;89(3):219–29.
- 21. Bao P, Kodra A, Tomic-Canic M, Golinko MS, Ehrlich HP, Brem H. The Role of Vascular Endothelial Growth Factor in Wound Healing. J Surg Res. 2009;153(2):347–58.
- 22. Gantwerker EA, Hom DB. Skin: Histology and Physiology of Wound Healing. Vol. 19, Facial Plastic Surgery Clinics of North America. 2011. p. 441–53.
- 23. Banaudha KK, Patnaik GK, Maheshwari RK. Curcumin enhances wound healing in streptozotocin induced diabetic rats and genetically diabetic mice. 1999;
- 24. Ross R, Bendıtt EP. Wound healing and collagen formation. I. Sequential changes in components of guinea pig skin wounds observed in the electron microscope. J Biophys Biochem Cytol. 1961;11:677–700.
- 25. Ross R. The fibroblast and wound repair. Biol Rev Camb Philos Soc. 1968;43(1):51–96.
- 26. Gülpak M. Deneysel Diyabet Modeli Oluşturulmuş Ratlarda Lavanta Yağının Yara İyileşmesine Etkisi. Doktora Tezi, Gazi Üniversitesi 2020
- 27. Menke NB, Ward KR, Witten TM, Bonchev DG, Diegelmann RF. Impaired wound healing. Clin Dermatol. 2007;25(1):19–25.
- 28. Mogosan C, Vostinaru O, Oprean R, Heghes C, Filip L, Balica G, et al. A comparative analysis of the chemical composition, anti-inflammatory, and antinociceptive effects of the essential oils from three species of Mentha cultivated in Romania. Molecules. 2017 Feb 1;22(2).
- 29. Atiyah AG. The role of Helianthus tuberosus powder in healing of full-thickness wounds in mice. 2021;14:1290–8.
- 30. Mathew-Steiner SS, Roy S, Sen CK. Collagen in wound healing. Bioengineering. 2021;8(5).
- 31. Fazil M, Nikhat S. Topical medicines for wound healing: A systematic review of Unani literature with recent advances. J Ethnopharmacol. 2020;257(April):112878.
- 32. Frank S, Hubner G, Breier G, Longaker MT, Greenhalgh DG, Werner S. Regulation of vascular endothelial growth factor expression in cultured keratinocytes. Implications for normal and impaired wound healing. Vol. 270, Journal of Biological Chemistry. 1995. p. 12607–13.
- 33. Shukla A, Dubey MP, Srivastava R, Srivastava BS. Differential expression of proteins during healing of cutaneous wounds in experimental normal and chronic models. Biochem Biophys Res Commun. 1998;244(2):434–9.
- 34. Brown LF, Yeo KT, Berse B, Yeo TK, Senger DR, Dvorak HF, et al. Expression of vascular permeability factor (vascular endothelial growth factor) by epidermal keratinocytes during wound Healing. J Exp Med. 1992;176(5):1375–9.
- 35. Zhang Z, Wang S, Diao Y, Zhang J, Lv D. Fatty acid extracts from Lucilia sericata larvae promote murine cutaneous wound healing by angiogenic activity. 2010;1–9.
- 36. Cibrian D, Fuente H De, Sánchez-madrid F. Metabolic Pathways That Control Skin Homeostasis and Inflammation. Trends Mol Med. 2020;1–12.
- 37. Antfolk D, Sjöqvist M, Cheng F, Isoniemi K, Duran CL, Rivero-Muller A, et al. Selective regulation of Notch ligands during angiogenesis is mediated by vimentin. Proc Natl Acad Sci U S A. 2017;114(23):E4574–81.
- 38. Kartenbeck J, Schwechheimer K, Moll R, Franke WW. Attachment of vimentin filaments to desmosomal plaques in human meningiomal cells and arachnoidal tissue. J Cell Biol. 1984;98(3):1072–81.
- 39. Franke WW, Moll R. Cytoskeletal components of lymphoid organs. Differentiation. 1987;36(2):145–63.
- 40. Battaglia RA, Delic S, Herrmann H, Snider NT. Vimentin on the move: New developments in cell migration [version 1; referees: 2 approved]. F1000Research. 2018;7(0):1–10.