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IntroductionAs an insulin sensitive tissue, the heart decreases glucose usage during fasting. This response is mediated, in part, by decreasing phosphofructokinase-2 (PFK-2) activity and levels of its product fructose-2,6-bisphosphate. However, the importance of fructose-2,6-bisphosphate in the fasting response on other metabolic pathways has not been evaluated.ObjectivesThe goal of this study is to determine how sustaining cardiac fructose-2,6-bisphosphate levels during fasting affects the metabolomic profile.MethodsControl and transgenic mice expressing a constitutively active form of PFK-2 (Glyco(Hi)) were subjected to either 12-h fasting or regular feeding. Animals (n=4 per group) were used for whole-heart extraction, followed by gas chromatography-mass spectrometry metabolic profiling and multivariate data analysis.ResultsPrincipal component analysis displayed differences between Control and Glyco(Hi) groups under both fasting and fed conditions while a clear response to fasting was observed only for Control animals. However, pathway analysis revealed that these smaller changes in the Glyco(Hi) group were significantly associated with branched-chain amino acid (BCAA) metabolism (similar to 40% increase in all BCAAs). Correlation network analysis demonstrated clear differences in response to fasting between Control and Glyco(Hi) groups amongst most parameters. Notably, fasting caused an increase in network density in the Control group from 0.12 to 0.14 while the Glyco(Hi) group responded oppositely (0.17-0.15).ConclusionsElevated cardiac PFK-2 activity during fasting selectively increases BCAAs levels and decreases global changes in metabolism.