The Effects of Novel Triazolopyrimidine Derivatives on H<sub>2</sub>S Production in Lung and Vascular Tonus in Aorta

Author:

Ozbek Emine Nur,Istanbullu Huseyin,Kızrak Umran,Alan Albayrak Elif,Sevin Gülnur,Yetik-Anacak Gunay

Abstract

<b><i>Introduction:</i></b> Hydrogen sulfide (H<sub>2</sub>S), known as a third gasotransmitter, is a signaling molecule that plays a regulatory role in physiological and pathophysiological processes. Decreased H<sub>2</sub>S levels were reported in inflammatory respiratory diseases such as asthma, chronic obstructive pulmonary disease, and pulmonary hypertension. H<sub>2</sub>S donors or drugs that increase H<sub>2</sub>S have emerged as novel treatments for inflammatory respiratory diseases. We previously showed that resveratrol (RVT) causes vascular relaxation and antioxidant effects by inducing H<sub>2</sub>S production. In the current study, we synthesized a new molecule Cpd2, as an RVT analog. We examined the effect of Cpd2 and its precursor chalcone compound (Cpd1) on H<sub>2</sub>S formation under both healthy and oxidative stress conditions in the lung, as well as vascular relaxation in the aorta. <b><i>Methods:</i></b> Cpd2 synthesized from Cpd1 with microwaved in basic conditions. H<sub>2</sub>S formation was measured by H<sub>2</sub>S biosensor in the mice lungs under both healthy and pyrogallol-induced oxidative stress conditions in the presence/absence of H<sub>2</sub>S synthesis inhibitor aminooxyacetic acid (AOAA). The effect of compounds on vascular tonus is investigated in mice aorta by DMT myograph. <b><i>Results:</i></b> RVT and Cpd2 significantly increased <sc>l</sc>-cysteine (<sc>l</sc>-cys) induced-H<sub>2</sub>S formation in the lung homogenates of healthy mice, but Cpd1 did not. Superoxide anion generator pyrogallol caused a decrease in H<sub>2</sub>S levels in mice lungs and Cpd2 restored it. Inhibition of Cpd2-induced H<sub>2</sub>S formation by AOAA confirmed that Cpd2 increases endogenous H<sub>2</sub>S formation in both healthy and oxidative stress conditions. Furthermore, we found that both Cpd1 and Cpd2 (10<sup>−8</sup>–10<sup>−4</sup> M) caused vascular relaxation in mice aorta. <b><i>Discussion and Conclusion:</i></b> We found that Cpd2, a newly synthesized RVT analog, is an H<sub>2</sub>S-inducing molecule and vasorelaxant similar to RVT. Since H<sub>2</sub>S has antioxidant and anti-inflammatory effects, Cpd2 has a potential for the treatment of respiratory diseases where oxidative stress and decreased H<sub>2</sub>S levels are present.

Publisher

S. Karger AG

Subject

Pharmacology,General Medicine

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