Effects of Endothelium-Derived Nitric Oxide on Renal Hemodynamics and Function in the Sheep Fetus View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1993-12

AUTHORS

Guy A Bogaert, Barry A Kogan, Robert A Mevorach

ABSTRACT

ABSTRACT: We investigated the effects of the endothelium-derived nitric oxide system on renal hemodynamics and function during the 3rd trimester in a chronically catheterized fetal sheep preparation. Acetylcholine caused a significant decrease in renal vascular resistance (60% of the baseline value) as compared with aortic constriction (142% of the baseline value). The effects of acetylcholine could be blocked by prior administration of Nω-nitro-L-arginine (renal vascular resistance = 102% of baseline). Sodium nitroprusside also caused a significant drop in renal vascular resistance (63% of baseline), but this could not be blocked by Nω-nitro-L-arginine (77% of baseline). Infusion of Nω-nitro-L-arginine with blood pressure maintained at a constant level resulted in a significant increase in renal vascular resistance (148% of the baseline value) as compared with saline alone (94% of baseline). Glomerular filtration rate increased after saline infusion (156% of the baseline value), but this increase was blocked by Nω-nitro-L-arginine (87% of baseline). Sodium excretion also increased (340%), and this increase was blunted by Nω-nitro-L-arginine (235%). We conclude that basal production of endothelium-derived nitric oxide results in ongoing renal vasodilation in 3rd-trimester fetal sheep, maintaining baseline renal blood flow. The endothelium-derived nitric oxide system can also be stimulated to an increased level of activity, and its blockade partially prevents the homeostatic response of the fetus to volume and salt overload. More... »

PAGES

755-761

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1203/00006450-199312000-00011

DOI

http://dx.doi.org/10.1203/00006450-199312000-00011

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1021403163

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/8108188


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