Vasorelaxant effect of propentofylline in isolated equine digital veins

• Published in: European journal of pharmacology 2013-10, Vol.718 (1-3), p.124-130
• Main Authors: Kabbesh, Nasr, Gogny, Marc, Chatagnon, Gérard, Noireaud, Jacques, Desfontis, Jean-Claude, Mallem, Mohamed Yassine
• Format: Article
• Language: English
• Subjects: adenosine; adenylate cyclase; Animals; antagonists; cGMP-dependent protein kinase; Colforsin - pharmacology; cyclic AMP; Cyclic AMP - metabolism; cyclic GMP; Cyclic GMP - metabolism; EDVs; Endothelium; Endothelium - drug effects; Endothelium - metabolism; Forelimb - blood supply; forskolin; guanylate cyclase; Horses; In Vitro Techniques; indomethacin; mechanism of action; Nitric oxide; nitric oxide synthase; nitroprusside; Nitroprusside - pharmacology; phenylephrine; Phenylephrine - pharmacology; Propentofylline; prostaglandin synthase; Receptors, Purinergic P1 - metabolism; Vasoconstriction - drug effects; Vasodilation - drug effects; Vasodilator Agents - pharmacology; Vasorelaxation; Veins - cytology; Veins - drug effects; Veins - physiology; Xanthines - pharmacology
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/j.ejphar.2013.09.003

We evaluated the vasorelaxant effect of propentofylline (PPF), a methylxanthine derivative, and its mechanism of action in equine digital veins (EDVs). Cumulative concentration-response curves to PPF (1nM–300µM) were recorded in phenylephrine-precontracted EDV rings under different experimental conditions. PPF-induced relaxation was partially inhibited by endothelium removal, but was unaltered by CGS-15943 (an adenosine receptor antagonist; 3µM). PPF-induced relaxation was partially inhibited in the presence of L-NAME (a nitric oxide (NO) synthase inhibitor; 100µM), ODQ (an inhibitor of soluble guanylyl cyclase; 30µM) or Rp-8-Br-PET-cGMP-S (a protein kinase G inhibitor; 3µM). It was not modified by indomethacin (a non-selective cyclooxygenase (COX) inhibitor; 10µM), and was slightly potentiated by H-89 (a protein kinase A inhibitor; 2µM). In endothelium-intact EDVs, PPF-induced relaxation was associated with a 2.4- and 24.1-fold increase in the tissue cGMP and cAMP content respectively. PPF (100μM) did not shift the concentration–response curve to phenylephrine (1nM–300µM) but reduced the maximal effect. To investigate whether PPF can affect cAMP- and cGMP-induced relaxations, relaxation curves to forskolin (an activator of adenylate cyclase) and to sodium nitroprusside (SNP, a NO donor) were recorded in EDV rings pretreated with PPF (100µM). PPF only slightly potentiated the forskolin-induced relaxation without affecting the SNP-induced relaxation. We demonstrated that PPF-induced relaxation in EDVs is partially endothelium-dependent. The PPF-induced relaxation partially occurred via NO release and both cAMP and cGMP generation, through COX-independent mechanisms but could also result from the inhibition of cAMP-phosphodiesterase activity for the highest concentrations. [Display omitted]