(Hypertension. 1999;33:924-926.)
© 1999 American Heart Association, Inc.
Scientific Contributions |
From INSERM U525, Hôpital Saint-Louis, Paris, France.
Correspondence to Dr Florent Soubrier, INSERM U525, Hôpital Saint-Louis, 1 Av Claude Vellefaux, 75475 Paris Cedex 10, France. E-mail soubrier@inserm.chu-stlouis.fr
| Introduction |
|---|
Two studies published in this issue illustrate the interest and the limits of this approach on 2 genes responsible for the enzymatic generation of nitric oxide (NO).1 2 Among the multiple actions of NO, those involving the cardiovascular system were extensively documented and designate the genes coding for NO-generating enzymes as candidate genes.3
Because, in the mammalian genome, 3 genes encoding 3 different nitric oxide synthases (NOS) are responsible for enzymatic generation of NO from L-arginine in various cells and under various stimuli, the role of each gene in NO generation defines its place as a candidate gene in hypertension.
Transgenic experiments supply the best arguments that the
endothelial NOS (eNOS) is a strong candidate since
pharmacological inhibition of this isoform is not available. Homozygous
mice for the knockout of the eNOS gene have a level of blood
pressure
15 mm Hg higher than control mice, a result obtained
independently by 2 groups.4 5 More recently, the
mouse eNOS cDNA was transduced in mice under the transcriptional
control of a heterologous endothelial celltargeting
promoter, the preproendothelin gene promoter.6 Basal
systolic and diastolic blood pressure were both
reduced by
20 mm Hg in
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