Ellagic Acid and Its Metabolites as Potent and Selective Allosteric Inhibitors of Liver Pyruvate Kinase

Author:

Battisti Umberto Maria12ORCID,Gao Chunixa12,Akladios Fady12,Kim Woonghee2,Yang Hong2,Bayram Cemil3,Bolat Ismail4,Kiliclioglu Metin4,Yuksel Nursena5,Tozlu Ozlem Ozdemir5ORCID,Zhang Cheng26,Sebhaoui Jihad7ORCID,Iqbal Shazia7,Shoaie Saeed28,Hacimuftuoglu Ahmet3,Yildirim Serkan4,Turkez Hasan9,Uhlen Mathias2,Boren Jan1011ORCID,Mardinoglu Adil28ORCID,Grøtli Morten1ORCID

Affiliation:

1. Department of Chemistry and Molecular Biology, University of Gothenburg, 412 96 Gothenburg, Sweden

2. Science for Life Laboratory, KTH–Royal Institute of Technology, 104 50 Stockholm, Sweden

3. Department of Medical Pharmacology, Faculty of Medicine, Atatürk University, Erzurum 25240, Turkey

4. Department of Pathology, Faculty of Veterinary, Atatürk University, Erzurum 25240, Turkey

5. Department of Molecular Biology and Genetics, Faculty of Science, Erzurum Technical University, Erzurum 25050, Turkey

6. School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China

7. Trustlife Labs, Drug Research & Development Center, Istanbul 34774, Turkey

8. Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King’s College London, London SE1 9RT, UK

9. Department of Medical Biology, Faculty of Medicine, Atatürk University, Erzurum 25240, Turkey

10. Department of Molecular and Clinical Medicine, University of Gothenburg, 405 30 Gothenburg, Sweden

11. Sahlgrenska University Hospital, 405 30 Gothenburg, Sweden

Abstract

Liver pyruvate kinase (PKL) has recently emerged as a new target for non-alcoholic fatty liver disease (NAFLD), and inhibitors of this enzyme could represent a new therapeutic option. However, this breakthrough is complicated by selectivity issues since pyruvate kinase exists in four different isoforms. In this work, we report that ellagic acid (EA) and its derivatives, present in numerous fruits and vegetables, can inhibit PKL potently and selectively. Several polyphenolic analogues of EA were synthesized and tested to identify the chemical features responsible for the desired activity. Molecular modelling studies suggested that this inhibition is related to the stabilization of the PKL inactive state. This unique inhibition mechanism could potentially herald the development of new therapeutics for NAFLD.

Funder

Knut and Alice Wallenberg Foundation

Swedish Research Council

Ogonoris Foundation

ScandiEdge Therapeutics

Torsten Söderberg Foundation

Publisher

MDPI AG

Subject

Food Science,Nutrition and Dietetics

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