Evaluation of cytotoxicity of methanolic extract from Zataria multiflora Boiss. and its fractions on the colorectal adenocarcinoma cell lines (Caco-2)

Authors

  • F. Sharififar Herbal and Traditional Medicines Research Center, Department of Pharmacognosy, Faculty of Pharmacy, Kerman University of Medical Sciences, Kerman, Iran.
  • M. Asgharian Rezee Pharmaceutics Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.
  • M. Miri-moghaddam* Department of Toxicology and Pharmacology, Faculty of Pharmacy, Kerman University of Medical Sciences, Kerman, Iran. Celluar & Molecular Research Center, Birjand University of Medical Sciences, Birjand, Iran.
Abstract:

Background and objectives: ZatariamultifloraBioss. (ZM) has shown several effects in gastrointestinal, respiratory and nervous system. In this study, the effect of Z. multiflora was examined in colon cancer cell lines of Caco-2. Methods: Total extract and petroleum ether, chloroform and methanol fractions of the plant were prepared using warm maceration method based on the complete phenolic compounds. Different concentrations were prepared and examined on caco2 cell lines using (MTT) assay. Results: The extract and fractions of the plant showed the lowest viability at the concentration of 250 μg/mL. In the total plant extract, the lowest viability was 44.6±8.9% in the cell line. In fractions of petroleum ether, chloroform and methanol, the lowest viabilities were (43.12±2.61% and 43.64±2.32% and 43.17±1.82%), respectively. All fractions showed toxicity to the cell line in a concentration dependent manner. The least IC50 was related to the petroleum ether and methanol fractions with IC50 value of (48.60±12.50 and 51.06±12.15 μg/mL) on Caco-2 cell line, respectively. Conclusion: Considering the results, toxicity of the plant was shown on Caco-2 cell line which was due to petroleum ether and methanol fractions and indicated that toxic components of the plant were from both polar and nonpolar ones.

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Journal title

volume 4  issue Supplement

pages  114- 114

publication date 2017-11-01

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