Aging blunts the dynamics of vasodilation in isolated skeletal muscle resistance vessels

Behnke BJ, Delp MD. Aging blunts the dynamics of vasodilation in isolated skeletal muscle resistance vessels. J Appl Physiol 108: 14-20, 2010. First published October 1, 2009; doi:10.1152/japplphysiol.00970.2009.-Aging is associated with an altered ability to match oxygen delivery (Q(O2)) to consumption ((V) over dot(O2)) in skeletal muscle and differences in the temporal profile of vasodilation may provide a mechanistic basis for the Q(O2)-to-(V) over dot(O2) mismatching during the rest-to-exercise transition. Therefore, we tested the hypothesis that the speed of vasodilation will be blunted in skeletal muscle first-order arterioles from old vs. young rats. Arterioles from the soleus and the red portion of the gastrocnemius (Gast(Red)) muscles were isolated from young (Y, 6 mo; n = 9) and old (O, 24 mo; n = 9) Fischer 344 rats and studied in vitro. Vessels were exposed to acetylcholine (ACh; 10(-6) M), sodium nitroprusside (SNP; 10(-4) M), and increased intraluminal flow, and the subsequent vasodilation was recorded at 30 frames/s. The data were fit to a monoexponential model and the dynamics of vasodilation [i.e., time delay, time constant (tau), and rate of change (delta/tau)] were calculated. With old age, the rate of vasodilation was significantly blunted in resistance vessels from the soleus to ACh (Y, 27.9 +/- 3.6; O, 8.8 +/- 2.6 mu m/s) and flow (Y, 12.8 +/- 2.1; O, 3.1 +/- 0.9 mu m/s). In the GastRed the old age-associated impairment of endothelium-dependent vasodilator dynamics was even greater than that of the soleus. With SNP neither the magnitude nor time constant of vasodilation was affected by age in either muscle. The results indicate that aging impairs the dynamics of vasodilation in resistance vessels from the soleus and GastRed muscles mediated, in part, through the endothelium. Thus the old age-associated slower rate and magnitude of vasodilation could inhibit the delivery of O-2 during the critical transition from rest to exercise in moderate to highly oxidative skeletal muscle.