| Literature DB >> 29925691 |
Pär Steneberg1, Emma Lindahl1, Ulf Dahl1, Emmelie Lidh1, Jurate Straseviciene1, Fredrik Backlund1, Elisabet Kjellkvist1, Eva Berggren2, Ingela Lundberg2, Ingela Bergqvist2, Madelene Ericsson3, Björn Eriksson2, Kajsa Linde2, Jacob Westman4, Thomas Edlund1,2, Helena Edlund1.
Abstract
AMPK activated protein kinase (AMPK), a master regulator of energy homeostasis, is activated in response to an energy shortage imposed by physical activity and caloric restriction. We here report on the identification of PAN-AMPK activator O304, which - in diet-induced obese mice - increased glucose uptake in skeletal muscle, reduced β cell stress, and promoted β cell rest. Accordingly, O304 reduced fasting plasma glucose levels and homeostasis model assessment of insulin resistance (HOMA-IR) in a proof-of-concept phase IIa clinical trial in type 2 diabetes (T2D) patients on Metformin. T2D is associated with devastating micro- and macrovascular complications, and O304 improved peripheral microvascular perfusion and reduced blood pressure both in animals and T2D patients. Moreover, like exercise, O304 activated AMPK in the heart, increased cardiac glucose uptake, reduced cardiac glycogen levels, and improved left ventricular stroke volume in mice, but it did not increase heart weight in mice or rats. Thus, O304 exhibits a great potential as a novel drug to treat T2D and associated cardiovascular complications.Entities:
Keywords: Cardiovascular disease; Diabetes; Metabolism
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Year: 2018 PMID: 29925691 PMCID: PMC6124394 DOI: 10.1172/jci.insight.99114
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708