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Products of Sulfide/Selenite Interaction Possess Antioxidant Properties, Scavenge Superoxide-Derived Radicals, React with DNA, and Modulate Blood Pressure and Tension of Isolated Thoracic Aorta

Selenium (Se), an essential trace element, and hydrogen sulfide (H(2)S), an endogenously produced signalling molecule, affect many physiological and pathological processes. However, the biological effects of their mutual interaction have not yet been investigated. Herein, we have studied the biologi...

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Detalles Bibliográficos
Autores principales: Grman, Marian, Misak, Anton, Kurakova, Lucia, Brezova, Vlasta, Cacanyiova, Sona, Berenyiova, Andrea, Balis, Peter, Tomasova, Lenka, Kharma, Ammar, Domínguez-Álvarez, Enrique, Chovanec, Miroslav, Ondrias, Karol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899273/
https://www.ncbi.nlm.nih.gov/pubmed/31885828
http://dx.doi.org/10.1155/2019/9847650
Descripción
Sumario:Selenium (Se), an essential trace element, and hydrogen sulfide (H(2)S), an endogenously produced signalling molecule, affect many physiological and pathological processes. However, the biological effects of their mutual interaction have not yet been investigated. Herein, we have studied the biological and antioxidant effects of the products of the H(2)S (Na(2)S)/selenite (Na(2)SeO(3)) interaction. As detected by the UV-VIS and EPR spectroscopy, the product(s) of the H(2)S-Na(2)SeO(3) and H(2)S-SeCl(4) interaction scavenged superoxide-derived radicals and reduced (·)cPTIO radical depending on the molar ratio and the preincubation time of the applied interaction mixture. The results confirmed that the transient species are formed rapidly during the interaction and exhibit a noteworthy biological activity. In contrast to H(2)S or selenite acting on their own, the H(2)S/selenite mixture cleaved DNA in a bell-shaped manner. Interestingly, selenite protected DNA from the cleavage induced by the products of H(2)S/H(2)O(2) interaction. The relaxation effect of H(2)S on isolated thoracic aorta was eliminated when the H(2)S/selenite mixture was applied. The mixture inhibited the H(2)S biphasic effect on rat systolic and pulse blood pressure. The results point to the antioxidant properties of products of the H(2)S/selenite interaction and their effect to react with DNA and influence cardiovascular homeostasis. The effects of the products may contribute to explain some of the biological effects of H(2)S and/or selenite, and they may imply that a suitable H(2)S/selenite supplement might have a beneficial effect in pathological conditions arisen, e.g., from oxidative stress.