4.6 Article

Anti-Obesity Evaluation of Averrhoa carambola L. Leaves and Assessment of Its Polyphenols as Potential α-Glucosidase Inhibitors

期刊

MOLECULES
卷 27, 期 16, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27165159

关键词

antidiabetic; Averrhoa carambola L; dihydrochalcone; flavone glycosides; obesity; Oxalidaceae; type 2 diabetes

资金

  1. Egyptian Cultural Affairs and Missions sector, Ministry of Higher Education, Egypt
  2. Leibniz Universitat Hannover

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The aqueous methanol leaf extract of Averrhoa carambola L. (CLK) was found to have significant anti-obese activity in an obese rat model. Fourteen compounds were isolated and identified, including new compounds not previously reported in A. carambola L. leaves and compounds isolated for the first time from the Family Oxalidaceae. Flavone glycosides showed potential as antidiabetic agents, while dihydrochalcone glycosides showed weaker activity.
Averrhoa carambola L. is reported for its anti-obese and anti-diabetic activities. The present study aimed to investigate its aqueous methanol leaf extract (CLL) in vivo anti-obese activity along with the isolation and identification of bioactive compounds and their in vitro alpha-glucosidase inhibition assessment. CLL improved all obesity complications and exhibited significant activity in an obese rat model. Fourteen compounds, including four flavone glycosides (1-4) and ten dihydrochalcone glycosides (5-12), were isolated and identified using spectroscopic techniques. New compounds identified in planta included (1) apigenin 6-C-(2-deoxy-beta-D-galactopyranoside)-7-O-beta-D-quinovopyranoside, (8) phloretin 3 '-C-(2-O-(E)-cinnamoyl-3-O-beta-D-fucopyranosyl-4-O-acetyl)-beta-D-fucopyranosyl-6 '-O-beta-D fucopyranosyl-(1/2)-alpha-L arabinofuranoside, (11a) phloretin3 '-C-(2-O-(E)-p-coumaroyl-3-O-beta-D-fucosyl-4-O-acetyl)-beta-D-fucosyl-6 '-O-(2-O-beta-D-fucosyl)-alpha-L-arabinofuranoside, (11b) phloretin3 '-C-(2-O-(Z)-p-coumaroyl-3-O-beta-D-fucosyl-4-O-acetyl)-beta-D-fucosyl-6 '-O-(2-O-beta-D-fucosyl)-alpha-L-arabinofuranoside. Carambolaside M (5), carambolaside Ia (6), carambolaside J (7), carambolaside I (9), carambolaside P (10a), carambolaside O (10b), and carambolaside Q (12), which are reported for the first time from A. carambola L. leaves, whereas luteolin 6-C-alpha-L-rhamnopyranosyl-(1-2)-beta-D-fucopyranoside (2), apigenin 6-C-beta-D-galactopyranoside (3), and apigenin 6-C-alpha-L-rhamnopyranosyl-(1-2)-beta-L-fucopyranoside (4) are isolated for the first time from Family. Oxalidaceae. In vitro alpha-glucosidase inhibitory activity revealed the potential efficacy of flavone glycosides, viz., 1, 2, 3, and 4 as antidiabetic agents. In contrast, dihydrochalcone glycosides (5-11) showed weak activity, except for compound 12, which showed relatively strong activity.

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