Op den Kamp 2022 Mol Metab

From Bioblast
Publications in the MiPMap
Op den Kamp YJM, Gemmink A, de Ligt M, Dautzenberg B, Kornips E, Jorgensen JA, Schaart G, Esterline R, Pava DA, Hoeks J, Schrauwen-Hinderling VB, Kersten S, Havekes B, Koves TR, Muoio DM, Hesselink MKC, Oscarsson J, Phielix E, Schrauwen P (2022) Effects of SGLT2 inhibitor dapagliflozin in patients with type 2 diabetes on skeletal muscle cellular metabolism. https://doi.org/10.1016/j.molmet.2022.101620

Β» Mol Metab 66:101620. PMID: 36280113 Open Access

Op den Kamp Yvo JM, Gemmink Anne, de Ligt Marlies, Dautzenberg Bas, Kornips Esther, Jorgensen Johanna A, Schaart Gert, Esterline Russell, Pava Diego A, Hoeks Joris, Schrauwen-Hinderling Vera B, Kersten Sander, Havekes Bas, Koves Timothy R, Muoio Deborah M, Hesselink Matthijs KC, Oscarsson Jan, Phielix Esther, Schrauwen Patrick (2022) Mol Metab

Abstract: SGLT2 inhibitors increase urinary glucose excretion and have beneficial effects on cardiovascular and renal outcomes; the underlying mechanism may be metabolic adaptations due to urinary glucose loss. Here, we investigated the cellular and molecular effects of 5 weeks of dapagliflozin treatment on skeletal muscle metabolism in type 2 diabetes patients.

Twenty-six type 2 diabetes mellitus patients were randomized to a 5-week double-blind, cross-over study with 6-8-week wash-out. Skeletal muscle acetylcarnitine levels, intramyocellular lipid (IMCL) content and phosphocreatine (PCr) recovery rate were measured by magnetic resonance spectroscopy (MRS). Ex vivo mitochondrial respiration was measured in skeletal muscle fibers using high resolution respirometry. Intramyocellular lipid droplet and mitochondrial network dynamics were investigated using confocal microscopy. Skeletal muscle levels of acylcarnitines, amino acids and TCA cycle intermediates were measured. Expression of genes involved in fatty acid metabolism were investigated.

Mitochondrial function, mitochondrial network integrity and citrate synthase and carnitine acetyltransferase activities in skeletal muscle were unaltered after dapagliflozin treatment. Dapagliflozin treatment increased intramyocellular lipid content (0.060 (0.011, 0.110) %, p=0.019). Myocellular lipid droplets increased in size (0.03 ΞΌm2 (0.01-0.06), p<0.05) and number (0.003 ΞΌm-2 (-0.001-0.007), p=0.09) upon dapagliflozin treatment. CPT1A, CPT1B and malonyl CoA-decarboxylase mRNA expression was increased by dapagliflozin. Fasting acylcarnitine species and C4-OH carnitine levels (0.4704 (0.1246, 0.8162) pmoles*mg tissue-1, p<0.001) in skeletal muscle were higher after dapagliflozin treatment, while acetylcarnitine levels were lower (-40.0774 (-64.4766, -15.6782) pmoles*mg tissue-1, p<0.001). Fasting levels of several amino acids, succinate, alpha-ketoglutarate and lactate in skeletal muscle were significantly lower after dapagliflozin treatment. Dapagliflozin treatment for 5 weeks leads to adaptive changes in skeletal muscle substrate metabolism favoring metabolism of fatty acid and ketone bodies and reduced glycolytic flux. β€’ Keywords: Acylcarnitines, Dapagliflozin, Mitochondrial function, Myocellular lipid metabolism, SGLT2i, TCA cycle intermediates β€’ Bioblast editor: Plangger M β€’ O2k-Network Lab: NL Maastricht Schrauwen P, US NC Durham Koves TR

Labels: MiParea: Respiration 

HRR: Oxygraph-2k 


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