New insights into the mechanisms of the vasorelaxant effects of apocynin in rat thoracic aorta. (11th January 2012)

• Record Type: Journal Article
• Authors: Senejoux, François; Girard‐Thernier, Corine; Berthelot, Alain; Bévalot, Françoise; Demougeot, Céline
• Is Part Of: Fundamental & clinical pharmacology. Volume 27:Number 3(2013:Jun.)
• Page Start: 262
• Page End: 270
• Publication Date: 2012-01-11
• Subjects: Pharmacology -- Periodicals; 615.1
• DOI: 10.1111/j.1472-8206.2011.01025.x
• Languages: English
• ISSNs: 0767-3981

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Apocynin is a naturally occurring acetophenone widely used as an inhibitor of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. Recent data suggested that apocynin might exert NADPH oxidase‐independent pharmacological properties. Among them, vasorelaxant properties have been described, but the mechanisms still give rise to debates. The present study investigated the mechanisms involved in the vasorelaxant effect of apocynin on the in vitro model of rat isolated thoracic aortic rings. Apocynin (30 μ<sc>m</sc> to 10 m<sc>m</sc>) induced a dose‐dependent relaxation in both endothelium‐intact and endothelium‐denuded aortic rings with respective EC<sub>50</sub> values of 0.78 ± 0.08 and 1.91 ± 0.21 m<sc>m</sc>. Endothelium removal or inhibition of nitric oxide (NO) synthase with <italic>N</italic><sup>ω</sup>‐nitro‐<sc>l</sc>‐arginine‐methyl ester (<sc>l</sc>‐NAME) significantly decreased but did not abolish the effect of apocynin. By contrast, apocynin‐induced relaxation was unchanged after incubation with indomethacin or charybdotoxin plus apamin. In endothelium‐denuded aortas, the vasorelaxant effect of apocynin was significantly reduced by glibenclamide but not by 4‐aminopyridine nor by iberiotoxin. Apocynin significantly decreased Ca<sup>2+</sup>‐induced contraction and inhibited intracellular Ca<sup>2+</sup>mobilization after contraction with phenylephrine. Finally, the acute intravenous injection of apocynin led to an immediate and transient hypotensive effect in spontaneously hypertensive rats (SHR). In conclusion, our data demonstrated that apocynin induces both endothelium‐independent relaxant effects involving inhibition of Ca<sup>2+</sup>mobilization and activation of K<sub>ATP</sub> channels in vascular smooth muscle cells and endothelium‐dependent effects mediated by NO. These results should provide a basis for caution when interpreting results on the vascular effects of apocynin.</p> </abstract>