Antileukemic, Antioxidant, Anti-Inflammatory and Healing Activities Induced by a Polyphenol-Enriched Fraction Extracted from Leaves of Myrtus communis L.
Hamza MechchateCarlos Eduardo de Castro AlvesImane Es-SafiAmal AmaghnoujeFatima Zahra JawhariRegiane Costa de OliveiraAlice de Freitas GomesRaffaele ConteGemilson Soares PontesDalila BoustaAndriy V GrafovPublished in: Nutrients (2022)
Natural products have offered a number of exciting approaches in cancer treatment over the years. In this study, we investigated the prophylactic and therapeutic effects of the polyphenol-enriched fraction extracted from Myrtus communis (PEMC) on acute and chronic leukemia. According to the UHPLC-MS n , the fraction is rich in flavonoids. Protective activity of the PEMC was assessed by evaluating the antioxidant, anti-inflammatory, wound healing, and hemolysis potential in a series of in vivo and in vitro assays, while the therapeutic approach consisted of the evaluation of cytotoxic activity of the PEMC against HL60 and K562 leukemia cell lines. Safety of the fraction was also evaluated on a non-cancerous Vero cell line and by an acute toxicity test performed in mice. The PEMC demonstrated a significant anti-inflammatory and healing potential. The activities found at the dose of 100 mg/kg were better than those observed using a reference drug. The PEMC demonstrated a significant antioxidant effect and a specific cytotoxicity towards HL60 (IC 50 = 19.87 µM) and K562 (IC 50 = 29.64 µM) cell lines being non-toxic to the Vero cell line. No hemolytic activity was observed in vitro and no toxicity effect was found in mice. Thus, the PEMC has a pharmacological potential as both preventive and therapeutic agent. However, further research is necessary to propose its mechanism of action.
Keyphrases
- anti inflammatory
- oxidative stress
- liver failure
- drug induced
- ms ms
- acute myeloid leukemia
- bone marrow
- respiratory failure
- wound healing
- multiple sclerosis
- human health
- type diabetes
- emergency department
- risk assessment
- metabolic syndrome
- skeletal muscle
- red blood cell
- tandem mass spectrometry
- adverse drug
- ultra high performance liquid chromatography