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

Nephrol Dial Transplant. 1998 Mar;13(3):594-601. doi: 10.1093/ndt/13.3.594.

Abstract

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 a marked reduction of 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Aging / physiology*
  • Animals
  • Antihypertensive Agents / pharmacology
  • Arginine / analogs & derivatives
  • Glomerular Filtration Rate
  • Hemodynamics
  • Kidney / blood supply
  • Kidney / physiology*
  • Kidney Function Tests
  • Male
  • Microspheres
  • Nitric Oxide / physiology*
  • Nitroprusside / pharmacology
  • Rats
  • Rats, Wistar

Substances

  • Antihypertensive Agents
  • Nitroprusside
  • Nitric Oxide
  • Arginine
  • Acetylcholine