Phytochemical Content and Anticancer Activity of Jamaican Dioscorea alata cv. White Yam Extracts

Author:

Wallace Kenroy12,Wright Racquel34,Williams-Longmore Melisa1,Wright Sasha-Gay15,Asemota Helen13

Affiliation:

1. Department of Basic Medical Sciences, Biochemistry Section, Faculty of Medical Sciences, The University of the West Indies, Mona, Kingston, Jamaica

2. College of Natural and Applied Science Allied Health and Nursing, Northern Caribbean University, Mandeville, Jamaica

3. Biotechnology Centre, Faculty of Science & Technology, The University of the West Indies, Mona, Kingston, Jamaica

4. Faculty of Engineering and Applied Technology, Caribbean Maritime University, Kingston, Jamaica

5. Faculty of Engineering, The University of the West Indies, Mona, Kingston, Jamaica

Abstract

Dioscorea spp. is known for its myriad medicinal properties. D. alata, specifically crude extracts, have displayed potent anticancer properties. However, the chemical constituents of these extracts have not been examined. The aim of this study is to determine the chemical composition and antioxidant characteristics of the active extracts from D. alata tuber. Chemoinformatic profiling of the Jamaican Dioscorea alata cultivar white yam tuber was generated by a sequential Soxhlet extraction of dried milled tuber, producing five crude extracts: hexane (E-1), diethyl ether (E-2), acetone (E-3), ethanol (E-4) and water (E-5). The analytes within the five extracts were dissolved in 0.1% DMSO and their anticancer activity was determined using DU145 prostate cancer cells. Both the acetone and the ethanolic extract were able to induce greater than 50% cell death at 50 µg/mL. The order of growth inhibition of the extracts in DU-145 cell is E3 (IC50, 10.81 µg/mL) > E-4 (IC50 24.17 µg/mL) > E-1 (IC50 > 100 µg/mL) ≥ E-2 (IC50 > 100 µg/mL) ≥ E-5 (IC50 > 100 µg/mL). Phytochemical screening of both E-3 and E-4 revealed the presence of all major classes of secondary metabolites except tannins. Resins were also absent in the E-3 extract. Phenolic quantification indicated that E-3 and E-4 possessed GAEs of 31 ± 1.1 and 72 ± 1.8 mg per g of sample, respectively. Inversely, E-3 displayed greater antioxidant capability with IC50 of 82.9 µg/mL compared to E-4 (166.9 µg/mL); however, neither was comparable to citric acid (33.6 µg/mL). The extract E-3 was further isolated by HPLC into 11 fractions. Fractions 4 and 5 possessed potent cell growth inhibitory effects. GCMs of fractions 4 and 5 showed they possessed numerous saturated fatty acids with pharmacological relevance. The presence of these compounds shows potential for exploitation of D. alata extracts for pharmacological purposes.

Funder

The University of the West Indies, Mona, Research and Publication grant

Publisher

MDPI AG

Subject

Filtration and Separation,Analytical Chemistry

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