Pharmacological vasodilation improves insulin-stimulated muscle protein anabolism but not glucose utilization in older adults
- Kyle L. Timmerman1,
- Jessica L. Lee1,
- Satoshi Fujita1,2,
- Shaheen Dhanani1,
- Hans C. Dreyer3,4,
- Christopher S. Fry4,
- Micah J. Drummond4,
- Melinda Sheffield-Moore1,2,
- Blake B. Rasmussen1,3,4 and
- Elena Volpi ()1,2
Objective. Skeletal muscle protein metabolism is resistant to the anabolic action of insulin in healthy, non-diabetic older adults. This defect is associated with impaired insulin-induced vasodilation and mTORC1 signaling. We hypothesized that, in older subjects, pharmacological restoration of insulin-induced capillary recruitment would improve the response of muscle protein synthesis and anabolism to insulin.
Research Design and Methods. Twelve healthy, non-diabetic older subjects (71±2 yrs) were randomized to two groups. Subjects were studied at baseline and during local infusion in one leg of insulin alone (Control) or insulin plus sodium nitroprusside (SNP) at variable rate to double leg blood flow. We measured leg blood flow by dye dilution; muscle microvascular perfusion with contrast enhanced ultrasound; Akt/mTORC1 signaling by Western blotting; and muscle protein synthesis, amino acid and glucose kinetics using stable isotope methodologies.
Results. There were no baseline differences between groups. Blood flow, muscle perfusion, phenylalanine delivery to the leg, and intracellular availability of phenylalanine increased significantly (P<0.05) in SNP only. Akt phosphorylation increased in both groups, but increased more in SNP (P<0.05). Muscle protein synthesis and net balance (NB) (nmol·min−1·100ml leg−1) increased significantly (P<0.05) in SNP (Synthesis: 43±6 to 129±25; NB: −16±3 to 26±12), but not in Control (Synthesis: 41±10 to 53±8, NB: −17±3 to −2±3).
Conclusion. Pharmacological enhancement of muscle perfusion and amino acid availability during hyperinsulinemia improves the muscle protein anabolic effect of insulin in older adults.
- Received March 26, 2010.
- Accepted August 6, 2010.
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