We found a clear trend towards lower baseline OCR and ATP production from oxidative phosphorylation ( Figures 8A, D ) with metformin treatment.
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Low glucose availability potentiates the effects of metformin on model T cell activation and exhaustion markers <i>in vitro</i>.
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Metformin treatment had no significant effect on IL-2 secretion after 24h, although a weak trend may be noted towards higher IL-2 levels at both 0.3 mM and 5 mM ( Figure 10C ; Supplementary Figure 7G ).
Low glucose even showed a trend towards lower mitochondrial mass.