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First published online on May 7, 2004.
Copyright © 2004 by The Physiological Society
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jphysiol.2004.064055v1
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Received March 5, 2004
Revised April 19, 2004
Accepted after revision May 4, 2004

Tetrahydrobiopterin Improves Endothelial Dysfunction and Vascular Oxidative Stress in Microvessels of Intrauterine Undernourished Rats

Maria do Carmo P Franco1*, Eliana H Akamine1, Zuleica B Fortes1, Elisa M Kawamoto1, Cristoforo Scavone1, Luiz Roberto Giorgetti Britto1, Marcelo N Muscara1, Simone A Teixeira1, Rita CA Tostes1, Maria Helena C Carvalho1, and Dorothy Nigro1

1 University of Sao Paolo

* To whom correspondence should be addressed. E-mail: mdcfranco{at}yahoo.com.

In the present study, we investigated the effects of the exogenous application of tetrahydrobiopterin on the endothelium-dependent vasorelaxation and superoxide anion generation in the mesenteric microvessels of intrauterine undernourished rats. In addition, we investigated the presence of peroxynitrite in these rats by evaluation of nitrotyrosine-containing proteins, a stable end-product of peroxynitrite oxidation. For this, female pregnant Wistar rats were fed either normal or 50% of the normal intake diets, during the whole gestational period. Male offspring (16-weeks of age) were studied for assessment of microvascular reactivity; hydroethidine staining assay; nitric oxide synthase (NOS) activity; nitric oxide (NO) measurement, Western blot analysis for nitrotyrosine-containing proteins and endothelial NOS (eNOS) mRNA expression. Superfusion with tetrahydrobiopterin significantly decreased superoxide generation and improved vascular function. Intrauterine malnutrition induced a decrement of NOS activity and NO production without affecting the gene expression of eNOS. However, incubation with tetrahydrobiopterin significantly improved NO production after stimulation with acetylcholine or bradykinin in intrauterine undernourished rats. The fact that the nitrotyrosine-containing proteins were increased could, at first sight, suggest that the peroxynitrite is the mediator responsible for the excessive oxidation and depletion of tetrahydrobiopterin. Our study shows that exogenous application of tetrahydrobiopterin leads to a significant improvement of endothelium-dependent vasodilatation, enhanced NO production and decreased superoxide generation in microvessels of intrauterine undernourished rats. Since we found decrease in NOS activity without alteration in gene expression of eNOS, we suggest that impaired NOS-dependent responses of mesenteric arterioles are related to impairment of tetrahydrobiopterin pathways.


Key words: Endothelium • Nitric oxide • Nitric oxide synthase







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