The Effects of Different Doses of Sildenafil on Coronary Blood Flow and Oxidative Stress in Isolated Rat Hearts

• Published in: Pharmaceuticals (Basel, Switzerland) Vol. 16; no. 1; p. 118
• Main Authors: Banjac, Nada, Vasović, Velibor, Stilinović, Nebojša, Tomas, Ana, Vasović, Lucija, Martić, Nikola, Prodanović, Dušan, Jakovljević, Vladimir
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01-01-2023; MDPI
• Subjects: Blood flow; coronary flow; Dosage and administration; Dose-response relationship (Biochemistry); Drug dosages; Health aspects; Heart; Ischemia; isolated rat heart; Kinases; Nitric oxide; Oxidative stress; Pharmacology, Experimental; phosphodiesterase; Physiological aspects; Sildenafil; Statistical significance; Serbia; phosphodiesterase; coronary flow; isolated rat heart; sildenafil; oxidative stress
• ISSN: 1424-8247; 1424-8247
• DOI: 10.3390/ph16010118

The dose-response relationship of sildenafil effects on cardiac function is not completely elucidated. The aim of this study was to assess the effects of different doses of sildenafil on coronary flow and oxidative stress in isolated rat hearts. Coronary flow and markers of oxidative stress, including nitrite outflow, and superoxide anion production in coronary effluent, were determined for isolated rat hearts. The experiments were performed during control conditions and in the presence of sildenafil (10, 20, 50, 200 nM) alone or with Nω-nitro-L-arginine monomethyl ester (L-NAME) (30 μM). Sildenafil was shown to result in a significant increase in coronary flow at lower coronary perfusion pressure (CPP) values at all administered doses, whereas, with an increase in CPP, a reduction in coronary flow was observed. An increase in nitric oxide (NO) was most pronounced in the group treated with the lowest dose of sildenafil at the highest CPP value. After the inhibition of the NO-cyclic guanosine monophosphate (cGMP) signaling (NOS) system by L-NAME, only a dose of 200 nM sildenafil was high enough to overcome the inhibition and to boost release of O
. That effect was CPP-dependent, with statistical significance reached at 80, 100 and 120 mmHg. Our findings indicate that sildenafil causes changes in heart vasculature in a dose-dependent manner, with a shift from a vasodilatation effect to vasoconstriction with a pressure increase. The highest dose administered is capable of producing superoxide anion radicals in terms of NOS system inhibition.