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Effect of marine red algal (Portieria hornemannii) extracts on starch digestion rate and its possible role in diabetes management
by
Unnikrishnan, P. S
, Jayasri, M. A
, Suthindhiran, K
in
Acetates
/ Acetone
/ Algae
/ Antioxidants
/ Ascorbic acid
/ Bioactive compounds
/ Blood cells
/ Enzymes
/ Erythrocytes
/ Macrophages
/ Seaweeds
/ Starch
2023
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Effect of marine red algal (Portieria hornemannii) extracts on starch digestion rate and its possible role in diabetes management
by
Unnikrishnan, P. S
, Jayasri, M. A
, Suthindhiran, K
in
Acetates
/ Acetone
/ Algae
/ Antioxidants
/ Ascorbic acid
/ Bioactive compounds
/ Blood cells
/ Enzymes
/ Erythrocytes
/ Macrophages
/ Seaweeds
/ Starch
2023
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Do you wish to request the book?
Effect of marine red algal (Portieria hornemannii) extracts on starch digestion rate and its possible role in diabetes management
by
Unnikrishnan, P. S
, Jayasri, M. A
, Suthindhiran, K
in
Acetates
/ Acetone
/ Algae
/ Antioxidants
/ Ascorbic acid
/ Bioactive compounds
/ Blood cells
/ Enzymes
/ Erythrocytes
/ Macrophages
/ Seaweeds
/ Starch
2023
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Effect of marine red algal (Portieria hornemannii) extracts on starch digestion rate and its possible role in diabetes management
Journal Article
Effect of marine red algal (Portieria hornemannii) extracts on starch digestion rate and its possible role in diabetes management
2023
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Overview
Marine algae (seaweeds) have emerged as a promising source in the continuing search for antidiabetic compounds because of their medicinal and nutritional properties. The present study evaluated marine red algae, Portieria hornemannii, for its inhibition of diabetic-linked enzymes (α-amylase, α-glucosidase, and DPP-IV) and antioxidant (DPPH) potential using in vitro assays. Among the tested extracts, ethyl acetate and acetone extract exhibited notable inhibition against α-amylase (IC50: 95.30 μg/mL), α-glucosidase (IC50: 632.5 μg/mL), and DPP-IV (IC50: 36.91 μg/mL). However, the antioxidant activity of the extracts was mild to moderate (17%). Furthermore, the half maximal inhibitory concentration (IC50) of the extracts was found to be non-toxic against mouse macrophage cells (J774) and human red blood cells. Chemical profiling by GC-MS analysis revealed the presence of major bioactive compounds such as phytol, z,z-6,28-heptatriactontadien-2-one, hentriacontane, and l-ascorbic acid. Overall, our findings indicate that the extracts of P. hornemannii reduce postprandial hyperglycemia by inhibiting the release of simple sugars through the inhibition of the enzymes (α-amylase, α-glucosidase, and DPP-IV).
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