Muscle extract of Arothron immaculatus regulates the blood glucose level and the antioxidant system in high-fat diet and streptozotocin induced diabetic rats
[Display omitted] •Ethanol extract of A. immaculatus showed excellent in vitro antioxidant activity.•LC-ESI/MS study showed the presence of antidiabetic compounds in muscle extracts.•Excellent in vivo antidiabetic activity against high-fat diet in STZ induced rat.•A. immaculatus muscle is recommende...
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Veröffentlicht in: | Bioorganic chemistry 2019-09, Vol.90, p.103072-103072, Article 103072 |
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Sprache: | eng |
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•Ethanol extract of A. immaculatus showed excellent in vitro antioxidant activity.•LC-ESI/MS study showed the presence of antidiabetic compounds in muscle extracts.•Excellent in vivo antidiabetic activity against high-fat diet in STZ induced rat.•A. immaculatus muscle is recommended to consume to reduce the diabetes burden.
In the present study pufferfish, Arothron immaculatus muscle methanol extract (AIME) was used to evaluate the antidiabetic activity against the high-fat diet (HFD) in streptozotocin (STZ) induced diabetic rat models. Initially, the In vitro antioxidant activity of the different muscle extract was evaluated which showed that AIME has higher efficiency to scavenge the free radicals. The animal study results revealed that the AIME could decrease the blood glucose level after 14 days of oral treatment and recover the animal from the severe progression of the disease. The LC-ESI/MS analysis of AIME extract revealed the presence of compounds such as docosahexaenoic acid, adrenic acid, docosanol, codeine and metoprolol. Among these compounds, docosahexaenoic acid, adrenic acid and docosanol are reported for its antidiabetic studies. Hence, the muscle is recommended to consume by humans as natural food in order to overcome the development of diabetes. This is the first study on the muscle extract of marine pufferfish which is used as antidiabetic agent to treat the diabetes-induced in the animal model. |
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ISSN: | 0045-2068 1090-2120 |
DOI: | 10.1016/j.bioorg.2019.103072 |