As of June 12, 2018 our Privacy Policy has been updated. For individuals in the European Union, CIL uses cookies on this website. Please review the new privacy statement to see how. By continuing to use this website you agree to us using cookies in accordance with our privacy statement. Click here for the new privacy statement..OK

Corporate Overview

IsoTopics™ - May 2022

Fructose Reprograms Glutamine-Dependent Oxidative Metabolism to Support LPS-Induced Inflammation

Jones, N.; Blagih, L.; Zani, F.; et al.

Fructose consumption has been demonstrated to exacerbate various non-communicable disorders; however, its metabolic and mechanistic impact on immune cells is not well established. This article examined how human monocytes and mouse macrophages respond metabolically and functionally to fructose exposure.  Among the experiments performed was MS-based metabolic analysis of cells cultured with stable isotope tracers (e.g., U-13C6 D-glucose, U-13C6 D-fructose). Overall, the works results have pathophysiological significance by showing, for the first time, that fructose promotes an inflammatory phenotype in both human and mouse mononuclear phagocytes.

Read article






Stable Isotope Newsletters | Cambridge Isotope Laboratories
stable isotope, stable isotope labeled compounds, environmental contaminant standards
CIL has been ready to help with the analytical standards critical to the task of defining and resolving any major environmental contamination problems.