This study has been conducted from April to September 2021, at the Institute of Veterinary and Agronomic Sciences, Batna - 1 University, and the Institute of Veterinary Sciences, University of Tiaret of Algeria.
Plant and ointment preparation
The flowering aerial parts of
Teucrium polium have been gathered in April 2021 from the region of Tiaret in Western Algeria, at 35°22¢15²N latitude and 1°19'01"E longitude. The plant was first authenticated by the forest conservation services of Tiaret, and then it was rinsed and left to shady dry at room temperature. Thereafter, the aerial parts of the plant were crushed using an electric grinder.
Fifty gram of the obtained powder was added to 300 ml of 70% methanol, and incubated in a shaking incubator (200 rpm) at 25°C for 72 h. After filtration of the extract, the flow-through was concentrated using rotary evaporator (Heidolph Laborota 4002-Germany), and a freeze dryer (Alpha 1-4 LSCbasic-Martin Christ-Germany). Finally, a 25% ointment was prepared by mixing 25 g of the plant concentrate to 100 g of ointment base composed of 5 g of hard paraffin, cetostearyl alcohol, wool fat and 85 g of white soft paraffin, as mentioned in British Pharmacopoeia (1988). The prepared ointment was stored in dark containers at 4°C.
Animals
For our experiment, we have used 20 healthy adult male
albino Wistar rats with an average weight of 180 g. The animals were purchased from the Pasteur Institute of Algeria. Prior to any procedure, the rats were adapted for 10 days in a clean, well ventilated and temperature-controlled room (25°C). The animals were kept in individual clear rodent cages with a stainless-steel cover where they received a standard rat pellet feed (UAB, El Kseur, Bejaia, Algeria) and
ad libitum water in rodent bottles. Sawdust was used as bedding and cleaning of cages and water bottles was carried out one in every 2 days.
Experimental design
Animals were randomly divided into two groups of 10 each: Control group (C) treated with the ointment base, and
Teucrium polium (TP) group treated with the plant ointment. Macroscopic evaluation of wound healing was based on measurement of wound surface and calculation of wound closure percentage for every three days once. Twenty-four days post treatment, a histological evaluation of the tissues formed at wound site was carried out. Finally, a statistical analysis of data obtained was performed to determine which group had the better healing.
Wound creation
Aseptic conditions were fully complied in all surgical procedures. Before surgery, rats were tranquilized in order to prepare the operative region. The back was therefore largely clipped and carefully shaved, taking care to avoid skin damage. No antiseptic was used on the shaved part. Animals were anesthetized with an intramuscular injection of Ketamine® at the rate of 80 mg/kg (Ketamine, Virbac, France) with Xylazine pro 2% @ 10 mg/kg (Xylazine, VETOPHARM Pro, Algeria) and then they were placed in sternal recumbency, and the skin to be excised was outlined. Using a scalpel blade, an incision through the entire depth of the skin was made along the markings. The skin was then gently excised using dissecting forceps and a pair of scissors. Minor bleeding was stopped with a sterile gauze buffered with normal saline. At the end of this procedure, an excisional wound of approximatively 600mm² was obtained. Wounds were left uncovered throughout the experimental period. Twenty-four hour post incised wound, treatment has been started as described in the experimental design section.
Measurement of wound surface and determination of wound closure percentage
After a deep tranquillization using 10 mg/kg of Xylazine, animals have been maintained in a sternal recumbency and the excisional wounds were photographed with an HD camera every three days. Wounds pictures were processed with Image-J software(https://imagej.nih.gov/ij/download.html) to measure the wound surfaces. The obtained results were finally used to calculate the percentage of wound closure according to the following formula:
Where
n= 3
rd, 6
th, 9
th, 12
th, 15
th, 18
th, 21
st, 24
th day of experiment.
Histological evaluation of wound healing
Animals were euthanized with an intracardiac injection of Propofol (Provive, El Kendi, Algeria). Samples of the scar tissue were then taken from the wound areas of each rat and were stored separately in 10% formalin solution (Formaldehyde, Sigma Aldrich, Germany) for 72h. After the usual histological treatment of the samples and their staining with hematoxylin and eosin, the prepared histological sections were subjected to microscopic observation in order to assess the degree of epithelialization, differentiation, amount of granulation tissue, inflammation, orientation of collagen fibers, and neovascularization. These observations were transformed into scores according to the modified scoring system based on previous models adapted by
Sultana et al., (1970) and
Abramov et al., (2007) (Table 1). Scores of histological parameters have been summed to calculate total histological score and determine which group had better healing.
Statistical analysis
Obtained results were statistically analyzed using Minitab 19 software on Windows. Means and standard deviations were calculated and then subjected to one-way analysis of variance (ANOVA) to determine the significant difference between the control group and the treatment group (
Teucrium polium). The Dunnett’s t-test was used to compare the scores recorded in both groups and a
p<0.05 was considered as statistically significant.