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Inhibitory Potential ofTurbinaria ornataagainst Key Metabolic Enzymes Linked to Diabetes
Author(s) -
P. S. Unnikrishnan,
K. Suthindhiran,
M. A. Jayasri
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/783895
Subject(s) - alpha glucosidase , dpph , enzyme , ic50 , chemistry , postprandial , biochemistry , in vivo , toxicity , dipeptidyl peptidase , amylase , traditional medicine , pharmacology , antioxidant , biology , diabetes mellitus , in vitro , medicine , microbiology and biotechnology , endocrinology , organic chemistry
One of the therapeutic approaches in treating diabetes is to reduce postprandial hyperglycemia by inhibiting major carbohydrate hydrolyzing enzymes. In the present study, crude extracts of marine seaweed, Turbinaria ornata , were tested for their antidiabetic potential using enzyme inhibitory assays ( α -amylase, α -glucosidase, and dipeptidyl peptidase-IV). Among the tested extracts, methanol and acetone extracts showed significant inhibitory effects on α -amylase (IC 50 250.9  μ g/mL), α -glucosidase (535.6  μ g/mL), and dipeptidyl peptidase-4 (55.2  μ g/mL), respectively. Free radical scavenging activity of these extracts was analyzed using DPPH assay (65%). Extracts were tested for in vitro toxicity using DNA fragmentation assay, haemolytic assay, and MTT assay. None of the extracts showed toxicity in tested models. Furthermore, GC-MS analysis of lead extracts showed the presence of major compounds, hentriacontane, z, z-6, 28-heptatriactontadien-2-one, 8-heptadecene, and 1-heptacosanol. Our findings suggest that Turbinaria ornata can be used as a potential source for further in vivo studies in controlling hyperglycemia.

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