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Bioactive Lignans from Zanthoxylum alatum Roxb. stem bark with cytotoxic potential
Minky Mukhija1, Kanaya Lal Dhar2, Ajudhia Nath Kalia2
1Punjab Technical University, Kapurthala, India; ISF College of Pharmacy, Ferozepur Road, Ghal Kalan, Moga 142001 Punjab, India.
Journal of Ethnopharmacology
|January 14, 2014
Summary
Zanthoxylum alatum stem bark exhibits significant cytotoxic potential against cancer cells. Researchers isolated three lignans, with 4'O demethyl magnolin showing the most potent anticancer activity, warranting further drug development.
Area of Science:
- Phytochemistry
- Pharmacology
- Cancer Research
Background:
- Zanthoxylum alatum possesses traditional medicinal uses for various ailments, including cancer.
- The plant's stem bark has been historically employed in folk medicine for treating numerous health conditions.
Purpose of the Study:
- To evaluate the cytotoxic potential of Zanthoxylum alatum stem bark extracts.
- To isolate and identify bioactive compounds responsible for the observed cytotoxic effects.
Main Methods:
- Cytotoxicity was assessed using MTT assay on lung (A549) and pancreatic (MIA-PaCa) carcinoma cell lines.
- Bioactive compounds were isolated via silica gel column chromatography and structures elucidated using spectroscopic techniques (UV, IR, NMR, Mass Spectrometry).
- Apoptosis induction was studied using acridine orange/ethidium bromide staining via fluorescence microscopy.
Main Results:
- The petroleum ether extract demonstrated significant cytotoxic activity.
- Three lignans, sesamin (A), kobusin (B), and 4'O demethyl magnolin (C), were isolated.
- Compound C (4'O demethyl magnolin) was identified as a novel, highly active cytotoxic agent, inducing apoptosis in MIA-PaCa cells at IC50 (21.72 µg/mL) and necrosis at higher doses.
Conclusions:
- Zanthoxylum alatum stem bark extract possesses notable cytotoxic potential.
- Isolated lignans, particularly 4'O demethyl magnolin, are responsible for the extract's anticancer properties.
- Zanthoxylum alatum represents a promising source for developing novel anticancer therapeutics.

