AMPK and Diseases: State of the Art Regulation by AMPK-Targeting Molecules

• Published in: Biology (Basel, Switzerland) Switzerland), 2022-07, Vol.11 (7), p.1041
• Main Authors: Tarasiuk, Olga, Miceli, Matteo, Di Domizio, Alessandro, Nicolini, Gabriella
• Format: Article
• Language: English
• Subjects: ADaM site; Alzheimer's disease; AMP; AMP mimicking; AMPK regulation; Antioxidants; Autophagy; Binding sites; Cancer; Cell growth; Diabetes mellitus; direct and indirect AMPK activators; Drug delivery; Drug development; Energy; Energy balance; Fatty acids; Glucose; Homeostasis; Intracellular; Isoforms; Kinases; Mammals; Metabolism; Molecular modelling; Oxidative stress; Phosphatase; Phosphorylation; Protein kinase; Protein synthesis; Proteins; Regulation; Review; Side effects; Signal transduction; Therapeutic targets
• ISSN: 2079-7737; 2079-7737
• DOI: 10.3390/biology11071041

5′-adenosine monophosphate (AMP)-activated protein kinase (AMPK) is an enzyme that regulates cellular energy homeostasis, glucose, fatty acid uptake, and oxidation at low cellular ATP levels. AMPK plays an important role in several molecular mechanisms and physiological conditions. It has been shown that AMPK can be dysregulated in different chronic diseases, such as inflammation, diabetes, obesity, and cancer. Due to its fundamental role in physiological and pathological cellular processes, AMPK is considered one of the most important targets for treating different diseases. Over decades, different AMPK targeting compounds have been discovered, starting from those that activate AMPK indirectly by altering intracellular AMP:ATP ratio to compounds that activate AMPK directly by binding to its activation sites. However, indirect altering of intracellular AMP:ATP ratio influences different cellular processes and induces side effects. Direct AMPK activators showed more promising results in eliminating side effects as well as the possibility to engineer drugs for specific AMPK isoforms activation. In this review, we discuss AMPK targeting drugs, especially concentrating on those compounds that activate AMPK by mimicking AMP. These compounds are poorly described in the literature and still, a lot of questions remain unanswered about the exact mechanism of AMP regulation. Future investigation of the mechanism of AMP binding will make it possible to develop new compounds that, in combination with others, can activate AMPK in a synergistic manner.