Effect of oyster mushroom powder on total leukocyte during inflammatory and proliferative phases of the wound healing process of third-degree burns model in Wistar rat (Rattus norvegicus)
Abstract
Burn wounds are challenging to treat because they often heal slowly and are susceptible to complications. The inflammatory phase plays an essential role in the repair process. However, prolonged inflammation can delay tissue healing. The total leukocyte count is an important parameter to evaluate the process, as it reflects the balance between inflammation and the initiation of tissue regeneration. Oyster mushrooms (Pleurotus ostreatus) contain β-glucans and phenolic compounds with anti-inflammatory and antioxidant properties, which may help regulate leukocyte activity and promote wound healing. This study aimed to evaluate the effect of oyster mushroom powder on total leukocyte counts during burn wound healing in Rattus norvegicus. Twenty-seven healthy male rats aged 2-3 mo were randomly divided into 3 groups, with 9 rats in each group. The negative control group received aquadest, the positive control group received bovine serum albumin, and the treatment group received 10% oyster mushroom powder. All groups received identical topical wound management with 1% silver sulfadiazine ointment to prevent infection and maintain a moist wound environment during healing. Blood samples were collected on days 0, 4, 8, and 12 after burn induction, and leukocyte counts were measured. The results showed that the treatment group consistently had lower leukocyte counts compared with control groups. On day 0, the treatment group had significantly lower leukocyte levels compared with the negative control (p = 0.019). On day 8, leukocyte counts in the treatment group were also significantly lower than the positive control (p = 0.030). By day 12, all groups showed a decrease, but the treatment group demonstrated the most gradual and stable reduction over time. In conclusion, oyster mushroom powder reduces leukocyte levels and supported a more controlled inflammatory phase, allowing faster progression to proliferation and improved burn wound healing.
References
Mulder PPG, Vlig M, Fasse E, Stoop MM, Pijpe A, van Zuijlen PPM, et al. Burn-injured skin is marked by a prolonged local acute inflammatory response of innate immune cells and pro-inflammatory cytokines. Front Immunol 2022;13:1034420.
https://doi.org/10.3389/fimmu.2022.1034420
Landén NX, Li D, Ståhle M. Transition from inflammation to proliferation: a critical step during wound healing. Cell Mol Life Sci. 2016;73(20):3861-85.
https://doi.org/10.1007/s00018-016-2268-0
Selvamani S, El Enshasy H, Dailin DJ, Malek RA, Hanapi SZ, Ambehabati KK, et al. Antioxidant compounds of the edible mushroom pleurotus ostreatus. Int J Biotech Wellness Ind 2018; 7: 1-14.
https://doi.org/10.6000/1927-3037.2018.07.01
Abdulhameed OA, Kadhim HM. Exploring the role of pleurotus ostreatus as an ointment formulation in inducing wound healing in mice skin. J Pharm Bioallied Sci 2024; 16: S243-6.
https://doi.org/10.4103/jpbs.jpbs_480_23
Rizzo JA, Thomas JM, Aden JK, Schauer SG, Van Gent JM, Peterson WC, et al. Decrease in total leukocyte count is associated with acute kidney injury after severe burn. J Burn Care Res. 2025;46(4):850-3.
https://doi.org/10.1093/jbcr/iraf039
Mulder PPG, Vlig M, Boekema BKHL, Stoop MM, Pijpe A, van Zuijlen PPM, et al. Persistent systemic inflammation in patients with severe burn injury is accompanied by influx of immature neutrophils and shifts in t cell subsets and cytokine profiles. Front Immunol. 2021;11:621222.
https://doi.org/10.3389/fimmu.2020.621222
Chandra P, Faizan M, Porwal M, Sharma H, Sachan N. An overview and review of growth factors in wound healing: emerging trends and innovations. Curr Diabetes Rev 2025; 27.
https://doi.org/10.2174/0115733998332692241202072249
Mulder PPG, Koenen HJPM, Vlig M, Joosten I, de Vries RBM, Boekema BKHL. Burn-induced local and systemic immune response: systematic review and meta-analysis of animal studies. J Invest Dermatol 2022;142(11):3093-109.e15.
https://doi.org/10.1016/j.jid.2022.05.004
Saravanan KG, Murugan SS, Eswaran A. Effect of pleurotus eous supplemented diets on the albumin, globulin and total proteins in experimental animal (male albino Wistar rats). Int. J. Pure App. Biosci SPI 2018;6(2): 239-44.
Duran-Güell M, Flores-Costa R, Casulleras M, López-Vicario C, Titos E, Díaz A, Alcaraz-Quiles J, et al. Albumin protects the liver from tumor necrosis factor α-induced immunopathology. FASEB J 2021;35(2):e21365.
https://doi.org/10.1096/fj.202001615RRR
Venter NG, Monte-Alto-Costa A, Marques RG. A new model for the standardization of experimental burn wounds. Burns 2015; 41: 542-7.
https://doi.org/10.1016/j.burns.2014.08.002
Elhusseiny SM, El-Mahdy TS, Elleboudy NS, Farag MMS, Aboshanab KM, Yassien MA. Immunomodulatory activity of extracts from five edible basidiomycetes mushrooms in Wistar albino rats. Sci Rep 2022;12(1):12423.
https://doi.org/10.1038/s41598-022-16349-2
Abazari M, Ghaffari A, Rashidzadeh H, Badeleh SM, Maleki Y. A systematic review on classification, identification, and healing process of burn wound healing. Int J Low Extrem Wounds 2022;21(1):18-30.
https://doi.org/10.1177/1534734620924857
Zheng B, Shen C, Sun J, Guo W, Jin Y, Niu Y. Developing a Simple burn model in rats of different ages. J Burn Care Res. 2019;40(5):639-47
https://doi.org/10.1093/jbcr/irz072
Devi MV, Poornima V, Sivagnanam UT. Wound healing in second-degree burns in rats treated with silver sulfadiazine: a systematic review and meta-analysis. J Wound Care 2022; 31: S31-45.
https://doi.org/10.12968/jowc.2022.31.Sup4.S31
Hoggatt J, Hoggatt AF, Tate TA, Fortman J, Pelus LM. Bleeding the laboratory mouse: Not all methods are equal. Exp Hematol 2016;44(2):132-7.e1.
https://doi.org/10.1016/j.exphem.2015.10.008
Beserra FP, Gushiken LFS, Hussni MF, Pellizzon CH. Regulatory mechanisms and chemical signaling of mediators involved in the inflammatory phase of cutaneous wound healing [Internet]. Wound healing - current perspectives. IntechOpen; 2019.
Devi PV, Islam J, Narzary P, Sharma D, Sultana F. Bioactive compounds, nutraceutical values and its application in food product development of oyster mushroom. J Fut Foods 2024; 4: 335-42.
https://doi.org/10.1016/j.jfutfo.2023.11.005
Lam YS, Okello EJ. Determination of lovastatin, β-glucan, total polyphenols, and antioxidant activity in raw and processed oyster culinary-medicinal mushroom, Pleurotus ostreatus (Higher Basidiomycetes). Int J Med Mushrooms 2015; 17: 117-28.
https://doi.org/10.1615/IntJMedMushrooms.v17.i2.30
Nworu CS, Ihim SA, Okoye FB, Esimone CO, Adikwu MU, Akah PA. Immunomodulatory and immunorestorative activities of β-D-glucan-rich extract and polysaccharide fraction of mushroom, Pleurutus tuberregium. Pharm Biol. 2015;53(11):1555-66.
https://doi.org/10.3109/13880209.2014.991838
Strudwick XL, Cowin AJ. The Role of the inflammatory response in burn injury [Internet]. Hot Topics in Burn Injuries. InTech; 2018.
https://doi.org/10.5772/intechopen.71330
Cañedo-Dorantes L, Cañedo-Ayala M. Skin acute wound healing: a comprehensive review. Int J Inflam 2019; 2019: 1-15.
https://doi.org/10.1155/2019/3706315
Pinar AA, Samuel CS. Immune mechanisms and related targets for the treatment of fibrosis in various organs. Curr Mol Med 2022; 22: 240-9.



