In:
American Journal of Physiology-Renal Physiology, American Physiological Society, Vol. 290, No. 4 ( 2006-04), p. F844-F853
Kurzfassung:
Experiments were performed to characterize renal hemodynamics in Thy-1 nephritic rats. A monoclonal antibody against Thy-1 was intravenously injected to induce mesangiolysis in rats, and 2 days later renal hemodynamic responses to variations in blood pressure were determined. In the first series of experiments, autoregulation of renal plasma flow (RPF) or glomerular filtration rate (GFR) was impaired in nephritic rats. In response to a reduction in blood pressure (98 ± 2 to 80 ± 1 mmHg), both RPF (4.17 ± 0.63 to 3.20 ± 0.45 ml·min −1 ·g kidney wt −1 , P 〈 0.05, n = 6) and GFR (0.88 ± 0.05 to 0.75 ± 0.06 ml·min −1 ·g kidney wt −1 , P 〈 0.05) were decreased in nephritic rats. Intravenous administration of furosemide and 30% albumin, both of which inhibit tubuloglomerular feedback, diminished renal autoregulation in control but not nephritic rats. In the second studies, the infusion of 5′-nucleotidase, an enzyme expressed on mesangial cells, into a renal artery ameliorated the magnitude of autoregulatory decrements in GFR in nephritic rats (−16 ± 5 to −6 ± 2%, P 〈 0.05, n = 6), but this enzyme failed to alter renal autoregulation in control rats. In the third studies, the effects of indomethacin were examined in nephritic rats. Inhibition of prostaglandin synthesis reduced RPF (4.07 ± 0.30 to 1.54 ± 0.22 ml·min −1 ·g kidney wt −1 , P 〈 0.05, n = 5) and GFR (1.03 ± 0.18 to 0.69 ± 0.13 ml·min −1 ·g kidney wt −1 , P 〈 0.05) in nephritic rats. However, cyclooxygenase inhibition failed to restore renal autoregulation in nephritic rats. Our results indicate that renal autoregulation is impaired in Thy-1 nephritis. Furthermore, the present data provide evidence that prostanoids contribute to maintain renal circulation in nephritic rats. Finally, our findings suggest that mesangial cells and/or 5′-nucleotidase plays an important role in mediating renal autoregulation.
Materialart:
Online-Ressource
ISSN:
1931-857X
,
1522-1466
DOI:
10.1152/ajprenal.00112.2005
Sprache:
Englisch
Verlag:
American Physiological Society
Publikationsdatum:
2006
ZDB Id:
1477287-5
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