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Nephrology Dialysis Transplantation, Vol 13, Issue 3 594-601, Copyright © 1998 by Oxford University Press


ORIGINAL ARTICLES

Role of nitric oxide-related mechanisms in renal function in ageing rats

D Tan, M Cernadas, P Aragoncillo, M Castilla, M Arroyo, A Farre, S Casad and C Caramelo
Laboratoire de Nefrologia, Fundacion Jimenez Diaz, Universidad Autonoma de Madrid, Reyes Catolicos 2, E-28040 Madrid,Spain; Servicio de Anatomia Patologica, Hospital Clinico de San Carlos, Universidad Complutense, Madrid, Spain; Corresponding author

Background: The impaired renal function and vasodilatation that accompany age need to be re-addressed based upon the new knowledge concerning vascular nitric oxide (NO)-dependent systems. The present study examined the effects of age on the NO-related renal response. Methods: The study was performed in euvolaemic, conscious Wistar rats, aged 5 and 18 months. Renal function and haemodynamic measurements with fluorescent microspheres were employed to assess differences between groups. Results: A first set of experiments showed that ageing rats had a reduced natriuretic and diuretic response to acetylcholine, whereas the response to sodium nitroprusside was preserved. In the same regard, a reduction of the renal functional effects of L-arginine (L-Arg) and L-glycine (L-Gly) was found in the older rats. In the ageing rats, these responses were accompanied by an enhanced effect of the L-Arg competitive analogue NwNLA, which provoked marked reduction on renal function. This effect of NwNLA was blocked by the simultaneous administration of a small dose of L-Arg in the ageing but not in the young rats. Systemic haemodynamic studies revealed that in ageing rats, NwNLA reduced renal blood flow and increased renal vascular resistances in a significantly higher proportion than in younger animals. However flow to other organs, namely, brain, spleen or liver, was affected in a similar manner in both young and old rats. Ultrastructural alterations were found in endothelial cells, which might constitute the anatomical basis for the observed functional derangements. Conclusions: The present experiments reveal that ageing is accompanied by significant differences in NO-related responses in the kidney which do not appear to affect blood flow to other organs. The response to L-Arg and L-Arg competitive analogues supports the existence of a marked dependency on NO-related mechanisms in the ageing rats, but not of a decreased baseline activity of the NO-dependent pathways. Key words: ageing; L-arginine; L-glycine; renal function
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