C. Hill et al., BASAL AND STIMULATED NITRIC-OXIDE IN CONTROL OF KIDNEY-FUNCTION IN THE AGING RAT, American journal of physiology. Regulatory, integrative and comparative physiology, 41(6), 1997, pp. 1747-1753
To investigate the activity of nitric oxide (NO) in control of renal h
emodynamics during aging, studies were conducted on conscious Sprague-
Dawley rats aged 3-5 mo (young, Y) and 18-22 mo (old, O). Blood pressu
re (BP) and renal vascular resistance (RVR) were higher in O vs. Y in
control, and acute systemic NO synthesis inhibition (NOSI) increased B
P and RVR, with an enhanced renal vasoconstrictor response in O. Infus
ion of the NO substrate L-arginine produced similar, selective renal v
asodilation in both groups. The endothelium-dependent vasodilator acet
ylcholine caused similar falls in BP and RVR, whereas sodium nitroprus
side produced an exaggerated depressor response in O vs. Y without fal
ls in RVR in either age group. Urinary excretion of the stable NO oxid
ation products (NOx) decreased with age, suggesting a decline in the o
verall somatic NO production. In conclusion, basal tonically produced
NO has a more pronounced role in maintenance of renal perfusion in agi
ng, whereas L-arginine- and agonist-stimulated renal vasodilation is n
ot impaired with age. NO production from some source may be reduced wi
th aging, as indicated by falls in 24-h NOx excretion, although the si
milarity in presser response and enhanced renal vasoconstrictor respon
se to NOSI suggests that the role of NO in control of total peripheral
and renal vascular resistance is maintained.