Comparative study of Teucrium extract and chlorhexidine in the healing and treatment of experimental oral ulcers
Subject Areas :
Journal of Large Animal Clinical Science Research(JLACSR)
Pejman Nazem zomorodi
1
,
loghman Akradi
2
,
Amir Farhad Kochak Asa’adi
3
1 - دانشکده دامپزشکی- گروه علوم درمانگاهی
2 - Department of Clinical Sciences, Faculty of Veterinary Medicine, Islamic Azad University, Sanandaj Branch, Iran
3 - Graduate, sanandaj Branch, Islamic Azad University, Sanandaj, Iran.
Received: 2021-08-20
Accepted : 2021-11-21
Published : 2021-11-22
Keywords:
Histopathology,
Healing,
Chlorhexidine,
Teucrium,
Wounds,
Abstract :
Background and Aim: The presence of any type of lesion in the mouth, such as injuries, sores or oral pests, in addition to causing pain in the area can cause the animal to not want to receive food as result, reduces weight and production. Teucrium is one of the medicinal plants that have effective healing properties in healing the mucosa. Therefore, the aim of this study was to compare comparative plant extract of Teucrium and chlorhexidine in the healing of experimental oral ulcers. Materials and Methods: In this experimental study, 36 New Zealand male rabbits were randomly divided into 3 equal groups: control without treatment (C), treatment group with 0.2% chlorhexidine (T1) and treatment group with hydroalcoholic extract of Teucrium (T2). In the beginning after anesthesia, the animals were placed in a supine position on the left side and the mouth of the animals was opened as much as possible by the mouth opener. Then, wound with a diameter of 3 mm was made on the gingival mucosa. Twice a day, the right gingival lesion was impregnated with a swab soaked in chlorhexidine solution (T1 group) and hydroalcoholic extract of Teucrium (T2 group). On days 1, 3, 7, and 14, the gums were sampled and the histopathological criteria for inflammatory cell infiltration, collagen filament arrangement, fibroblast cell presence, vascular formation, and epithelial tissue rearrangement were assessed. Also, the macroscopic diameter of the gingival tissue wound was measured on the mentioned days.Results: In T1 and T2 groups, the criteria for inflammatory cell infiltration, arrangement of collagen and vascular formation and rearrangement of epithelial tissue on days 7 and 14 showed a significant change compared to C group (P < 0.05). In the C group, the criteria of inflammatory cell infiltration increased during the study. In T1 and T2 groups, the macroscopic diameter of gingival tissue ulcer showed a significant decrease compared to C group (P < 0.05).Conclusion: This study showed that Teucrium extract can accelerate experimental wound healing.
References:
AL, A. A. H. S. (2020). Prophylaxis and therapeutic ability of inactivated dermatophytic vaccine against dermatophytoses in rabbit as an animal model.
Ansari, M., Alizadeh, A. M., Paknejad, M., Khaniki, M., & Naeimi, S. M. (2009). Effects of teucrium polium honey on burn wound healing process. Journal of Babol University of Medical Sciences, 11(3), 7-12.
Aragona, M., Dekoninck, S., Rulands, S., Lenglez, S., Mascré, G., Simons, B. D., & Blanpain, C. (2017). Defining stem cell dynamics and migration during wound healing in mouse skin epidermis. Nature communications, 8(1), 1-14.
Bolla, J. R., Howes, A. C., Fiorentino, F., & Robinson, C. V. (2020). Assembly and regulation of the chlorhexidine-specific efflux pump AceI. Proceedings of the National Academy of Sciences, 117(29), 17011-17018.
Brown, S. A., Rosenthal, K. L. (1997), Small Mammals: Self-Assessment Color Review. CRC Press.
Dar, R. A., Shahnawaz, M., & Qazi, P. H. (2017). General overview of medicinal plants: A review. The Journal of Phytopharmacology, 6(6), 349-351.
DeFilipps, R. A., & Krupnick, G. A. (2018). The medicinal plants of Myanmar. PhytoKeys(102), 1.
Desjardins-Park, H. E., Foster, D. S., & Longaker, M. T. (2018). Fibroblasts and wound healing: an update: Future Medicine.
Dudding, T., Haworth, S., Lind, P. A., Sathirapongsasuti, J. F., Tung, J. Y., Mitchell, R., . . . Elsworth, B. (2019). Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. Nature communications, 10(1), 1-12.
El Atki, Y., Aouam, I., Taroq, A., Lyoussi, B., Taleb, M., & Abdellaoui, A. (2019). Total phenolic and flavonoid contents and antioxidant activities of extracts from Teucrium polium growing wild in Morocco. Materials Today: Proceedings, 13, 777-783.
Fiorillo, L. (2019). Chlorhexidine gel use in the oral district: A systematic review. Gels, 5(2), 31.
Fossum, T. W. (2013), Small Animal Surgery 4th edition. Elsevier Health Sciences.
He, J., Liang, Y., Shi, M., & Guo, B. (2020). Anti-oxidant electroactive and antibacterial nanofibrous wound dressings based on poly (ε-caprolactone)/quaternized chitosan-graft-polyaniline for full-thickness skin wound healing. Chemical Engineering Journal, 385, 123464.
Khoramian Tusi, S., Manzari Tavakoli, Z., Bahram Abadi Nejhad, R., & Zeynali, B. (2014). Evaluation of teucrium polium mouthwash effect on salivary streptococcus mutans count. Journal of Mashhad Dental School, 38(4), 321-330.
Mehrabani, D., Rezaee, A., Azarpira, N., Fattahi, M. R., Amini, M., Tanideh, N., . . . Saberi-Firouzi, M. (2009). The healing effects of Teucrium polium in the repair of indomethacin-induced gastric ulcer in rats. Saudi Med J, 30(4), 494-499.
Niazian, M. (2019). Application of genetics and biotechnology for improving medicinal plants. Planta, 249(4), 953-973.
Oguntibeju, O. O. (2018). Medicinal plants with anti-inflammatory activities from selected countries and regions of Africa. Journal of inflammation research, 11, 307.
Othman, M. B., Salah-Fatnassi, K. B. H., Ncibi, S., Elaissi, A., & Zourgui, L. (2017). Antimicrobial activity of essential oil and aqueous and ethanol extracts of Teucrium polium L. subsp. gabesianum (LH) from Tunisia. Physiology and Molecular Biology of Plants, 23(3), 723-729.
Peimani, A., Keshavarz, S., Eslammanesh, T., & Sheikh Fathollahi, M. (2017). Comparison of 0.2 chlorhexidine gel and 10 betadine on healing of tooth socket in mice. Journal of Mashhad Dental School, 41(4), 295-304.
Robinson, N. B., Krieger, K., Khan, F. M., Huffman, W., Chang, M., Naik, A., . . . Girardi, L. N. (2019). The current state of animal models in research: A review. International journal of surgery, 72, 9-13.
Rodrigues, M., Kosaric, N., Bonham, C. A., & Gurtner, G. C. (2019). Wound healing: a cellular perspective. Physiological reviews, 99(1), 665-706.
Salimnejad, R., Sazegar, G., Borujeni, M. J. S., Mousavi, S. M., Salehi, F., & Ghorbani, F. (2017). Protective effect of hydroalcoholic extract of Teucrium polium on diabetes-induced testicular damage and serum testosterone concentration. International Journal of Reproductive BioMedicine, 15(4), 195.
Shedoeva, A., Leavesley, D., Upton, Z., & Fan, C. (2019). Wound healing and the use of medicinal plants. Evidence-Based Complementary and Alternative Medicine, 2019.
Sjöqvist, S., Ishikawa, T., Shimura, D., Kasai, Y., Imafuku, A., Bou-Ghannam, S., . . . Kanai, N. (2019). Exosomes derived from clinical-grade oral mucosal epithelial cell sheets promote wound healing. Journal of Extracellular Vesicles, 8(1), 1565264.
Tusi, S. K., Jafari, A., Marashi, S. M. A., Niknam, S. F., Farid, M., & Ansari, M. (2020). The effect of antimicrobial activity of Teucrium Polium on Oral Streptococcus Mutans: a randomized cross-over clinical trial study. BMC Oral Health, 20(1), 1-8.
Xu, D.-P., Li, Y., Meng, X., Zhou, T., Zhou, Y., Zheng, J., . . . Li, H.-B. (2017). Natural antioxidants in foods and medicinal plants: Extraction, assessment and resources. International journal of molecular sciences, 18(1), 96.
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