1. Mechanisms underlying the vasorelaxant effect of hydrogen sulfide on human saphenous vein
- Author
-
Predrag Milojevic, Hai-Tao Hou, Dragoslav Nenezic, Guo-Wei He, Ivan Stojanovic, Aleksandra Novakovic, Qin Yang, Marija Marinko, and Vladimir Kanjuh
- Subjects
Potassium Channels ,Vasodilator Agents ,hydrogen sulfide ,Vasodilation ,Sodium hydrosulfide ,Prostacyclin ,Pharmacology ,Apamin ,030226 pharmacology & pharmacy ,Glibenclamide ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,medicine ,Humans ,Saphenous Vein ,Pharmacology (medical) ,Channel blocker ,Hydrogen Sulfide ,Phenylephrine ,vasorelaxation ,Dose-Response Relationship, Drug ,NO pathway ,Iberiotoxin ,chemistry ,human saphenous vein ,K+ channels ,030217 neurology & neurosurgery ,medicine.drug - Abstract
Hydrogen sulfide (H2 S) represents the third and the youngest member of the gaseous transmitters family. The dominant effect of H2 S on isolated vessels is vasodilation. As the mechanism of H2 S-induced relaxation in human vessels remains unclear, the present study aimed to investigate the effects of H2 S donor, sodium hydrosulfide (NaHS), on isolated human saphenous vein (HSV) and to determine the mechanism of action. Our results showed that NaHS (1 µM-3 mM) induced a concentration-dependent relaxation of endothelium-intact HSV rings pre-contracted by phenylephrine. Pre-treatment with L-NAME, ODQ and KT5823 significantly inhibited NaHS-induced relaxation, while indomethacin induced partial inhibition. Among K+ channel blockers, the combination of apamin and TRAM-34 significantly affected the relaxation produced by NaHS, while iberiotoxin and glibenclamide only reduced maximal relaxation of HSV. NaHS partially relaxed endothelium-intact rings pre-contracted by high K+ , as well as phenylephrine-contracted rings in the presence of nifedipine. Additionally, the incubation of HSV rings with NaHS increased NO production. These results demonstrate that NaHS produces the concentration- and endothelium-dependent relaxation of isolated HSV. Vasorelaxation to NaHS probably involves activation of NO/cGMP/PKG pathway and partially prostacyclin. In addition, different K+ channels subtypes, especially SKCa and IKCa , as well as BKCa and KATP channels in high concentrations of NaHS, probably participate in the NaHS-induced vasorelaxation.
- Published
- 2021
- Full Text
- View/download PDF