The PDK1 Inhibitor Dichloroacetate Controls Cholesterol Homeostasis Through the ERK5/MEF2 Pathway

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2017
Author
Khan, Abrar Ul Haq
Allende-Vega, Nerea
Gitenay, Delphine
Gerbal-Chaloin, Sabine
Gondeau, Claire
Vo, Dang-Nghiem
Belkahla, Sana
Orecchioni, Stefania
Talarico, Giovanna
Bertolini, Francesco
Bozić Stanojević, Milica
Valdivielso Revilla, José Manuel
Bejjani, Fabienne
Jariel, Isabelle
Lopez-Mejia, Isabel C.
Fajas, Lluis
Lecellier, Charles-Henri
Hernandez, Javier
Daujat, Martine
Villalba, Martin
Suggested citation
Khan, Abrar Ul Haq; Allende-Vega, Nerea; Gitenay, Delphine; Gerbal-Chaloin, Sabine; Gondeau, Claire; Vo, Dang-Nghiem; ... Villalba, Martin. (2017) . The PDK1 Inhibitor Dichloroacetate Controls Cholesterol Homeostasis Through the ERK5/MEF2 Pathway. Scientific Reports, 2017, vol. 7, p. 10654. https://doi.org/10.1038/s41598-017-10339-5.
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Abstract
Controlling cholesterol levels is a major challenge in human health, since hypercholesterolemia can lead to serious cardiovascular disease. Drugs that target carbohydrate metabolism can also modify lipid metabolism and hence cholesterol plasma levels. In this sense, dichloroacetate (DCA), a pyruvate
dehydrogenase kinase (PDK) inhibitor, augments usage of the glycolysis-produced pyruvate in the mitochondria increasing oxidative phosphorylation (OXPHOS). In several animal models, DCA decreases plasma cholesterol and triglycerides. Thus, DCA was used in the 70 s to treat diabetes mellitus, hyperlipoproteinemia and hypercholesterolemia with satisfactory results. However, the mechanism of action remained unknown and we describe it here. DCA increases LDLR mRNA and protein levels as well as LDL intake in several cell lines, primary human hepatocytes and two different mouse models. This effect is mediated by transcriptional activation as evidenced by H3 acetylation on lysine 27 on the LDLR promoter. DCA induces expression of the MAPK ERK5 that turns on the transcription factor MEF2. Inhibition of this ERK5/MEF2 pathway by genetic or pharmacological means decreases LDLR expression and LDL intake. In summary, our results indicate that DCA, by inducing OXPHOS, promotes ERK5/MEF2 activation leading to LDLR expression. The ERK5/MEF2 pathway offers an interesting pharmacological target for drug development.
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http://hdl.handle.net/10459.1/62933
DOI
https://doi.org/10.1038/s41598-017-10339-5
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Scientific Reports, 2017, vol. 7, p. 10654
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cc-by (c) Khan, Abrar Ul Haq et al., 2017
Except where otherwise noted, this item's license is described as cc-by (c) Khan, Abrar Ul Haq et al., 2017