Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5588405 | Metabolism | 2017 | 9 Pages |
Abstract
Taken together, isonitramine inhibited α-glucosidase activity and PEPCK expression, while increased insulin expression, resulting in attenuating the postprandial hyperglycemia. Also, isonitramine protected the pancreas from ROS-mediated toxicities. Therefore, isonitramine may be a new drug candidate for the treatment of diabetes mellitus.
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Authors
So Jung Kwon, Su Jung Hwang, Yeonghun Jung, Hyeung-geun Park, Mi-hyun Kim, Yohan Park, Hyo-Jong Lee,