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Antitumour principles from Peganum harmala seeds
F Lamchouri1, A Settaf, Y Cherrah
1Laboratoire de Pharmacologie et Toxicologie, Faculté de médecine et de Pharmacie de Rabat, Maroc.
Summary
Peganum harmala seed alkaloids show significant antitumour potential. In vitro studies demonstrated high toxicity to cancer cells, while in vivo experiments confirmed antineoplastic activity, suggesting a novel anticancer therapy.
Area of Science:
- Pharmacology and Phytochemistry
- Natural Product Chemistry
- Oncology
Background:
- Peganum harmala, a medicinal plant, has historical uses but limited research on its antitumour properties.
- Traditional Moroccan medicine utilizes Peganum harmala seeds for skin and subcutaneous tumors.
- Existing research focuses on antibacterial, antifungal, and antiviral effects, not anticancer activity.
Purpose of the Study:
- To investigate the antineoplastic properties of Peganum harmala seed extracts.
- To evaluate the in vitro and in vivo antitumour activity of Peganum harmala alkaloids.
- To explore the potential of Peganum harmala as a novel anticancer therapy.
Main Methods:
- In vitro testing of varying concentrations (10-120 µg/ml) of Peganum harmala alkaloid extracts on four human tumor cell lines (Med-mek, UCP-Med carcinoma, UCP-Med sarcoma, Sp2/O-Ag14).
- In vivo experiments using the Sp2/O cell line grafted subcutaneously in BALB/c mice.
- Administration of the active alkaloid principle at 50 mg/kg orally for 40 days in mice.
Main Results:
- Peganum harmala alkaloid extracts significantly reduced tumor cell line proliferation in vitro within 24 hours.
- Complete tumor cell death was observed within 48-72 hours, demonstrating high in vitro cytotoxicity.
- Significant antitumoural activity was observed in vivo with oral administration of the active principle.
Conclusions:
- Peganum harmala alkaloids exhibit potent in vitro cytotoxicity against various tumor cell lines.
- The plant's alkaloids possess significant in vivo antitumour activity.
- Peganum harmala alkaloids represent a promising candidate for novel anticancer therapies.