The effect of medical-grade honey or hypericum on matrix metalloproteinases expression in feline wound healing


K Chatzimisios
V Tsioli
C Dovas
G Kazakos
E Moutou
V Angelou
E Pratsinakis
L Papazoglou
Resumen

The aim of the present study was to evaluate the relation between MMP expression and the local application of medical-grade honey or Hypericum in second-intention cutaneous wound healing in healthy cats.  Our hypothesis was that MMP expression may be affected by medical-grade honey or Hypericum application in cutaneous wounds in cats. Eight female spayed purpose-bred healthy DSH cats were included in the study. Under general isoflurane anesthesia eight 2 X 2 cm square wounds, four on each side of the dorsal midline were created full-thickness including the subcutaneous fat until the thoracolumbar fascia was apparent. The four wounds on each side were randomized to receive treatment or serve as untreated controls using computer software (random number generator).  Two of the wounds were treated daily with medical-grade honey ointment [LMS] two were treated daily with Hypericum-based ointment (HYP) two were used as untreated controls for medical-grade honey (LMSC), and two were used as untreated controls for Hypericum-based ointment (HYPC). The LMS and HYP treatments were applied aseptically once daily for 25 days. Biopsies were obtained from the two cranial wounds for MMPs measurements on day 0 and from the two caudal wounds for MMPs measurements on days 14 and 25. An evaluation of the expression of MMP-2, MMP-9, and TIMP-1 by real-time PCR was performed to investigate their association with the different measurement days. MMP-2, MMP-9, and TIMP-1 expressions did not differ between the LMS and HYP-treated wounds. No significant differences between sampling days for MMP-2 MMP-9 and TIMP-1 expressions were noted in all treated and control wounds (P= 0.188, 0.580, and 0.407 respectively). In conclusion, MMP-1, MMP-9, and TIMP-1 expressions were not affected by medical-grade honey or Hypericum applied locally in cutaneous wounds in cats. 

Article Details
  • Sección
  • Research Articles
Descargas
Los datos de descargas todavía no están disponibles.
Biografía del autor/a
V Tsioli, Clinic of Surgery, School of Veterinary Medicine, University of Thessaly, 224 Trikalon Street, Box Office 199, 43100 Karditsa, Greece

Clinic of Surgery, School of Veterinary Medicine, University of Thessaly, 224 Trikalon Street, Box Office 199, 43100 Karditsa, Greece

G Kazakos, Unit of Anaesthesiology and Intensive Care, Companion Animal Clinic, School of Veterinary Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, 54627 Thessaloniki, G

reece

Citas
Angelou V, Psalla D, Dovas CI, Kazakos GM, Marouda C, Chatzimisios
K, Kyrana Z, Moutou E, Karayannopoulou M, Papazoglou LG (2022)
Locally injected autologous platelet-rich-plasma improves cutaneous
wound healing in cats. Animals 12: 1-21.
Baker AH, Edwards DR, Murphy G (2002) Metalloproteinase inhibitors:
biological actions and therapeutic opportunities. J Cell Sci 115: 3719-
Bischofberger AS, Dart CM, Parkins NR, Dart AJ (2011) A preliminary
study on the effect of manuka honey on second intention healing of
contaminated wounds on the distal aspect of the forelimbs of horses.
Vet Surg40: 898-902.
Bischofberger AS, Dart CM, Parkins NR, Kelly A, Jeffcot L, Dart AJ
(2013) The effect of short- and long-term treatment with manuka honey on second intention healing of contaminated and noncontaminated
wounds on the distal aspect of the forelimbs in horses. Vet Surg 42:
-160.
Bohling MW, Henderson RA (2006) Differences in cutaneous wound
healing between dogs and cats. Vet Clin Small Anim 36: 687-692.
Bohling MW, Henderson RA, Swaim SF, Kincaid SA, Wright JC (2004)
Cutaneous wound healing in the cat: a macroscopic description and
comparison with cutaneous wound healing in the dog. Vet Surg 33:
-587.
Bohling MW, Henderson RA, Swaim SF, Kincaid SA, Wright JC (2006)
Comparison of the role of the subcutaneous tissues in cutaneous
wound healing in the dog and cat. Vet Surg35: 3-14.
Davidson JR (2015) Current concepts in wound management and wound
healing products. Vet Clin Small Anim 45: 537-564.
Gill SE, Parks WC (2007) Metalloproteinases and their inhibitors: regulators of wound healing. Intern J Biochem Cell Biol 40: 1334-1347.
Jursza, E, Skarzynski, DJ, Siemieniuch MJ (2014) Validation of reference
genes in the feline endometrium. Reprod Biol 14: 302-306.
Kandhwal M, Behl T, Singh S, Sharma N, Arora S, Bhatia S, Al-Harrasi
A, Sachdeva M, Bungau S (2022) Role of matrix metalloproteinase in
wound healing. Am J Transl Res 14: 4391-4405.
Kessler Y, Helfer-Hungerbuehler AK, Cattori V, Meli ML, Zellweger
B, Ossent P, Riond B, Reusch CE, Lutz H, Hofmann-Lehmann R
(2009) Quantitative TaqMan®real-time PCR assays for gene expression normalisation in feline tissues. BMC Mol Biol 10,https://doi.
org/10.1186/1471-2199-10-106.
Konstantinidis AO, Adamama-Moraitou KK, Pardali D,Dovas CI, Brellou
GD, Papadopoulos T, Jergens AE, Allespach K, Rallis TS (2021) Colonic mucosal and cytobrush sample cytokine mRNA expression in
canine inflammatory bowel disease and their correlation with disease
activity, endoscopic and histopathologic score. Plos one.16: 1-20.
Krejner A,Litwiniuk M, Grzela T (2016) Matrix metalloproteinases in the
wound microenvironment: Therapeutic perspectives. Chronic Wound
Care Manag Res 3: 29–39.
Lazaro JL, Izzo V, Meaume S, Davies AH, Lobmann R, Uccioli L (2016)
Elevated levels of matrix metalloproteinases and chronic wound
healing: an updated review of clinical evidence. J Wound Care25:
-287.
Lukanc B, Potokar T, Erjavec V (2018) Observational study of the effect
of L-Mesitran medical honey on wound healing in cats. VeterinarskiArciv 88: 59-74.
Lukanc B, Potokar T, Erjavec V (2020) Complete skin regeneration with
medical honey after skin loss on the entire circumference of a leg in a
cat. J Tissue Viability 29: 148-152.
Majtan J (2014) Honey an immunomodulator in wound healing Wound
Repair Regen 22: 187-192.
Mandel HH, Sutton GA, Abu E, Kelmer G (2020) Intralesional application of medical grade honey improves healing of surgically treated
lacerations in horses. Equine Vet J 52: 41-45.
Marino G, Pugliese M, Pecchia F, Garufi G, Lupo V, Di Giorgio S, Sfacteria A (2021) Conservative treatments for feline fibroadenomatous
changes of the mammary gland. Open Vet J11: 680-685.
Mehta CR,Patel NR (2010) IBM SPSS Exact tests.SPSS Inc: pp1-226.
Molan PC (1999) The role of honey in the management of wounds. J
Wound Care 8: 415-418.
Pavletic MM (2018) Basic principles of wound healing. In: Atlas of Small
Animal Wound Management and Reconstructive Surgery. 4th ed, Willey Blackwell, Hoboken: pp 17-31.
Penning LC, Vrieli Vet ImmunolImmunopathol 120: 212-222.
Petznick A, Madigan MC, Garrett Q, Sweeney DF, Evans MD (2013)
Contributions of ocular surface components to matrix-metalloproteinases (MMP)-2 and MMP-9 in feline tears following corneal epithelial wounding. PLoS One 8: 1-9.
Pleeging CCF, Coenye T, Mossialos D, De Rooster H, Chrysostomou D,
Wagener FADTG, CremersNAJ (2020) Synergistic antimicrobial activity of supplemented medical grade honey against Pseudomonas
Aeruginosa biofilm formation and eradication. Antibiotics 9: 1-16.
Repellin RL, Pitt KA, Lu M, Welker J, Noland EL, Stanley BJ (2021) The
effects of a proprietary Manuka honey and essential oil hydrogel on
the healing of acute full-thickness wounds in dogs, Vet Surg50:1634-
Sabino F, Auf Dem Keller U (2015) Matrix metalloproteinases in impaired wound healing. Metalloproteinases in Medicine 2: 1-8.
Samadi S, Khadivzaden T, Enami A, Mousavi NS, Tafaghodi M,
Behnaman HR (2010) The effect of hypericum perforatum on the
wound healing and scar of cesarian. J Alternat Complement Med16:
-117.
Schmittgen TD, Livak KJ (2008) Analyzing real-time PCR data by the
comparative C(T) method. Nat Protoc 3:1101–1108.
Tarlton JF, Vickery CJ, Leaper DJ, Bailey AJ (1997) Postsurgical wound
progression monitored by temporal changes in the expression of matrix metalloproteinase 9. Br J Dermatol 137:506–516.
Tresch M, Mevissen M, Ayrle H, Melzig M, Roosje P, Walkenhorst M
(2019) Medicinal plants as therapeutic options for topical treatment
in canine dermatology? A systematic review. BMC Vet Res15: 1-19.
Vatnikov Y, Shabunin S, Kulikov E, Karamyan A, Lenchenko E, Sachivkina N, Bobkova N, Bokov D, Zhilkina V, Tokar A, Shopinsaya
M, Rudenko P (2020). Effectiveness of biologically active substances
from Hypericum Perforatum L. in the complex treatment of purulent
wounds. Int J Pharm Res12: 1108-1117.
Volk SW, Bohling MW (2013) Comparative wound healing-Are the small
animal veterinarian’s clinical patients an improved translational model for human wound healing research? Wound Rep Reg21: 372-381.
Yadollah-Damavandi S, Chavoshi-Nejad M, Jangholi E,Nekouyian N,
Hosseini S, Seifaee A, Rafiee S, Karimi H, Askani-Esfani S, Parsa Y,
Mohsenikia M (2015) Topical Hypericum perforatum Improves Tissue Regeneration in Full-Thickness Excisional Wounds in Diabetic
Rat Model. Evid Based Complement Alternat Med 2015: 1-4.
Zhang Y, Lin J X, Vilcek J (1988) Synthesis of interleukin-6 (interferon
β2B cell stimulatory factor 2) in human fibroblasts is triggered by an
increase in intracellular cyclic AMP. J Biol Chem. 263: 6177-6182.
Xue M, Le NTV, Jackson CJ (2006) Targeting matrix metalloproteinases
to improve cutaneous wound healing. Expert OpinTher Targets 10:
Artículos más leídos del mismo autor/a