Maurer, J.* ; Zhao, X.* ; Irmler, M. ; Gudiksen, A.* ; Pilmark, N.S.* ; Li, Q.* ; Goj, T.* ; Beckers, J. ; Hrabě de Angelis, M. ; Birkenfeld, A.L. ; Peter, A. ; Lehmann, R. ; Pilegaard, H.* ; Karstoft, K.* ; Xu, G.* ; Weigert, C.
Redox state and altered pyruvate metabolism contribute to a dose-dependent metformin-induced lactate production of human myotubes.
Am. J. Physiol.-Cell Physiol. 325, C1131-C1143 (2023)
Metformin-induced glycolysis and lactate production can lead to acidosis as a life-threatening side effect, but slight increases in blood lactate levels in a physiological range were also reported in metformin-treated patients. However, how metformin increases systemic lactate concentrations is only partly understood. Because human skeletal muscle has a high capacity to produce lactate, the aim was to elucidate the dose-dependent regulation of metformin-induced lactate production and the potential contribution of skeletal muscle to blood lactate levels under metformin treatment. This was examined by using metformin treatment (16-776 μM) of primary human myotubes and by 17 days of metformin treatment in humans. As from 78 µM, metformin induced lactate production and secretion and glucose consumption. Investigating the cellular redox state by mitochondrial respirometry, we found metformin to inhibit the respiratory chain complex I (776 µM, P < 0.01) along with decreasing the [NAD+]:[NADH] ratio (776 µM, P < 0.001). RNA sequencing and phospho-immunoblot data indicate inhibition of pyruvate oxidation mediated through phosphorylation of the pyruvate dehydrogenase (PDH) complex (39 µM, P < 0.01). On the other hand, in human skeletal muscle, phosphorylation of PDH was not altered by metformin. Nonetheless, blood lactate levels were increased under metformin treatment (P < 0.05). In conclusion, the findings suggest that metformin-induced inhibition of pyruvate oxidation combined with altered cellular redox state shifts the equilibrium of the lactate dehydrogenase (LDH) reaction leading to a dose-dependent lactate production in primary human myotubes.NEW & NOTEWORTHY Metformin shifts the equilibrium of lactate dehydrogenase (LDH) reaction by low dose-induced phosphorylation of pyruvate dehydrogenase (PDH) resulting in inhibition of pyruvate oxidation and high dose-induced increase in NADH, which explains the dose-dependent lactate production of differentiated human skeletal muscle cells.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Typ der Hochschulschrift
Herausgeber
Schlagwörter
Lactate ; Metformin ; Pyruvate Dehydrogenase Complex ; Respiration ; Skeletal Muscle; Respiratory Complex I; Skeletal-muscle; Lactic-acidosis; Dehydrogenase; Phosphorylation; Inhibition; Activation; Therapy
Keywords plus
Sprache
englisch
Veröffentlichungsjahr
2023
Prepublished im Jahr
0
HGF-Berichtsjahr
2023
ISSN (print) / ISBN
0363-6143
e-ISSN
1522-1563
ISBN
Bandtitel
Konferenztitel
Konferzenzdatum
Konferenzort
Konferenzband
Quellenangaben
Band: 325,
Heft: 4,
Seiten: C1131-C1143
Artikelnummer: ,
Supplement: ,
Reihe
Verlag
American Physiological Society
Verlagsort
6120 Executive Blvd, Suite 600, Rockville, Md, United States
Tag d. mündl. Prüfung
0000-00-00
Betreuer
Gutachter
Prüfer
Topic
Hochschule
Hochschulort
Fakultät
Veröffentlichungsdatum
0000-00-00
Anmeldedatum
0000-00-00
Anmelder/Inhaber
weitere Inhaber
Anmeldeland
Priorität
Begutachtungsstatus
Peer reviewed
POF Topic(s)
90000 - German Center for Diabetes Research
30201 - Metabolic Health
Forschungsfeld(er)
Helmholtz Diabetes Center
Genetics and Epidemiology
PSP-Element(e)
G-502400-001
G-500600-004
G-500600-001
Förderungen
King Christian X Foundation
Research Foundation of Rigshospitalet(Denmark)
Aase and Ejnar Danielsen Foundation
Key Foundation from the National Natural Science Foundation of China
Mobility Programme of the Sino-German Center for Research Promotion
German Federal Ministry of Education and Research (BMBF)
Copyright
Erfassungsdatum
2023-11-28