Healing Potentials of Nigerian Bee Propolis on Meticillin- Resistant Staphylococcus Aureus Infected Skin Wound of Wistar Rats

This study evaluated the effects of Nigerian Bee Propolis extract on Methicillin Resistance Staphylococcus Aureus (MRSA) infected skin wounds of albino rats. Two full thickness circular wounds were created each on the dorsum of eighteen (18) healthy adult male albino rats with mean body weight of 126±7.09g. Each wound was contaminated with 108 colony forming unit of MRSA. The rats were then randomized into three (3) treatment groups (n=6) with topical application of Propolis extract (PE Group), Silver sulphadiazine (SS Group) and untreated Control (UT Group). Gross wound healing indices (exudation, edema, hyperemia, wound contraction), histopathologic (granulation, angiogenesis, fibroplasia, epithelialization) and immunologic healing indices were evaluated using standard methods. Bacteria clearance was through culture and quantification. The wound surface exudation and edge edema and hyperemia were prominent in all the groups from day 0 to 6 but persisted in the untreated group till day 12. Wound contraction was gradual in all the groups from day 0-18, it was higher between days 0 and 3 in the PE and SS than the UT group (P<0.05). Complete wound closure occurred on SS (day 15), and PE (day 16). The histopathological changes observed showed neutrophils regressed on day 6 to 18 in all groups and was faster in PE and SS groups (P<0.05). Platelets reduction was ` gradual from days 3 to 18 in all groups and was absent from days 6 to 18 in the PE group. Nigerian Bee propolis has a profound bacteria clearance and healing effect on wound infected with methicillin resistant staphylococcus aureus (MRSA) comparable to silver sulphadiazine and therefore recommended for infected wound treatment.

The effect of bee prepolis on primary dysmenorrhea: a randomized clinical trial

OBJECTIVE: Primary dysmenorrhea typically occurs with no associated pelvic pathology and is common in adolescents and young women. This study evaluated the effect of bee propolis on relief of primary dysmenorrhea. METHODS: The study was performed in 2018 in Hamadan, in western Iran, among female students with primary dysmenorrhea. Participants were randomly divided into two groups, using balanced block randomization, and were administered a placebo or bee propolis capsules for 5 days during two menstruation cycles. The number of participants required was estimated to be 86 in total, with 43 students in each group according to the inclusion criteria. We used the visual analog scale to assess pain severity. The independent t-test was conducted for comparing between two groups, using SPSS 16.0. RESULTS: A significant change was found in the mean pain scores during the first (P<0.001) and second (P<0.001) months after using bee propolis in comparison with placebo. The means of the pain scores in the bee propolis group were 5.32±2.28 and 4.74±2.40 in first and second months after the intervention, respectively, whereas the means of the pain scores in the placebo group were 7.40±1.21 and 7.17±1.24 in first and second months after the intervention, respectively. CONCLUSION: Our study showed that the use of bee propolis for two months compared with placebo reduced primary dysmenorrhea during the first and second months after use, with no adverse effects. Therefore, it could be used as an alternative to nonsteroidal anti-inflammatory drugs for relief of primary dysmenorrhea.

Evaluation of the in vitro antimicrobial activity of alcoholic solution and aqueous extract of bee propolis against enterococcus faecalis

AIM: The purpose of this study was to analyze the in vitro antimicrobial activity of aqueous and alcoholic extracts of propolis at 1% and 3% concentrations against Enterococcus faecalis (ATCC® 19433). MATERIAL AND METHODS: Initially, the microbial suspension was seeded in a Brain Heart Infusion Agar (BHIA) culture medium, distributed in 20 Petri dishes. Then, 4 soaked filter paper discs were placed on the surface of the inoculated medium of each plate for 1 minute in 1 mL of the following substances: C+ (positive control, n=20): 2% chlorhexidine gel; C- (negative control, n=20): saline solution; S1 (n=10): 1% bee propolis alcoholic solution; S2 (n=10): 3% bee propolis alcoholic solution; E1 (n=10): 1% aqueous propolis extract; E2 (n=10): 3% aqueous propolis extract. One filter paper disc of each (C+, C-, S1 and S2) was placed in a set of 10 Petri dishes, whereas one filter paper disc of each (C+, C-, E1 and E2) was placed in the other set of 10 Petri dishes. RESULTS: The results obtained after incubation at 37°C for 24 hours under microaerobic conditions revealed that S2 showed higher mean levels of microbial growth inhibition as compared to E1, E2 and S1. There were no significantly statically differences between the groups, except for the S2 group and C- group. Mean levels in all other groups were lower than in the C+ group. CONCLUSION: The study concluded that 1% and 3% bee propolis alcoholic solution had lower antibacterial activity against Enterococcus faecalis as compared to 2% chlorhexidine gel.

In vitro Evaluation of Antidermatophytic Activity of Egyptian Bee Propolis in Combination with Plant Essential Oils in Sheep Hoof Plate: An Experimental Model

Bee propolis ethanolic extract with some plant essential oils was investigated for its antidermatophytic properties. The tested plant essential oils included jasmine, clove, lemon, Arabian jasmine, mint, rosa, olive and basil. The antidermatophytic activity has been compared to Naftifine-HCl and Clotrimazole used for dermatophyte treatment. Experimental model has been tested using sheep hoof plate for the in vitro tests to stimulate human nails. Mint, clove and basil with 4 mg/ml of bee propolis have a comparable efficacy to those of Naftifine-HCl and Clotrimazole. There is a great necessity for new effective low price and safe antidermatophyte agents to avoid recurrent infection. Propolis synergistic could be of great importance with essential oils of plants in dermatophyte therapy.