Serotonin modulates hepatic 6-phosphofructo-1-kinase in an insulin synergistic manner.


Human and rat hepatic tissue express many serotonin (5-HT) receptor subtypes, such as 5-HT(1B), 5-HT(2A), 5-HT(2B) and 5-HT(7) receptors, which mediate diverse effects. 5-HT is known to regulate several key aspects of liver biology including hepatic blood flow, innervations and wound healing. 5-HT is also known to enhance net glucose uptake during glucose infusion in fasted dogs, but little is known about the ability of 5-HT to control hepatic glucose metabolism, especially glycolysis. This study addresses the potential of 5-HT to regulate PFK activity and the mechanisms related to the enzyme activity. Based on our results, we are the first to provide evidence that 5-HT up-regulates PFK in mouse hepatic tissue. Activation of the enzyme occurs through the 5-HT(2A) receptor and phospholipase C (PLC), resulting in PFK intracellular redistribution and favoring PFK association to the cytoskeletal f-actin-enriched fractions. Interestingly, 5-HT and insulin act in a synergistic manner, likely because of the ability of insulin to increase fructose-2,6-bisphosphate because the presence of this PFK allosteric regulator enhances the 5-HT effect on the enzyme activity. Together, these data demonstrate the ability of 5-HT to control hepatic glycolysis and present clues about the mechanisms involved in these processes, which may be important in understanding the action of 5-HT during the hepatic wound healing process.

DOI: 10.1016/j.biocel.2011.10.010
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@article{Coelho2012SerotoninMH, title={Serotonin modulates hepatic 6-phosphofructo-1-kinase in an insulin synergistic manner.}, author={Wagner Santos Coelho and Daniel Schuch da Silva and M{\^o}nica Mesquita Marinho-Carvalho and Mauro Sola-Penna}, journal={The international journal of biochemistry & cell biology}, year={2012}, volume={44 1}, pages={150-7} }