Fa. Dinenno et al., Reductions in basal limb blood flow and vascular conductance with human ageing: role for augmented alpha-adrenergic vasoconstriction, J PHYSL LON, 536(3), 2001, pp. 977-983
1. Basal whole-limb blood flow and vascular conductance decrease with age i
n men. We determined whether these age-associated changes in limb haemodyna
mics are mediated by tonically augmented sympathetic alpha -adrenergic vaso
constriction.
2. Seven young (28 +/- 2 years; mean +/- S.E.M) and eight older (64 +/- 2 y
ears) healthy, normotensive adult men were studied. Baseline femoral artery
blood flow (Doppler ultrasound) and calculated vascular conductance were 2
9 and 31 % lower, respectively, and vascular resistance was 53 % higher in
the older men (all P < 0.001).
3. Local (intra-femoral artery) alpha -adrenergic receptor blockade with ph
entolamine evoked greater increases in femoral blood flow (105 +/- 11 vs. 6
0 +/- 6 %) and vascular conductance (125 +/- 13 vs. 66 +/- 7 %), and reduct
ions in vascular resistance (55 +/- 2 vs. 39 +/- 3 %) in the experimental l
imb of the older compared with the young men (all P < 0.001). As a result,
alpha -adrenergic receptor blockade eliminated the significance of the age-
associated differences in absolute levels of femoral blood flow (500 +/- 51
vs. 551 +/- 35 ml min(-1)), vascular conductance (6.02 +/- 0.73 vs. 6.33 /- 0.26 U), and vascular resistance (0.17 +/- 0.03 vs. 0.16 +/- 0.01 U; P =
0.4-0.8, n.s.). Femoral haemodynamics in the control limb were unaffected
by phentolamine administration in the contralateral (experimental) limb. Co
mplete alpha -adrenergic receptor blockade was demonstrated by the absence
of vasoconstriction in the experimental limb in response to the cold presso
r test. Local propranolol was administered to control for any beta -adrener
gic effects of phentolamine. Propranolol did not affect haemodynamics in th
e experimental or control limbs.
4. Our results indicate that the age-related reductions in basal limb blood
flow and vascular conductance are mediated largely by chronically elevated
sympathetic alpha -adrenergic vasoconstriction. This may have important ph
ysiological and pathophysiological implications for the ageing human.