19th World Congress of Basic & Clinical Pharmacology 2023, Glasgow, İngiltere, 2 - 07 Temmuz 2023, ss.1124-1227
Introduction Hydrogen sulfide (H2S) is a gaseous signaling molecule with an inhibitory effect in the gastrointestinal system. We previously demonstrated the relaxant effect of NaHS and L-Cysteine and the role of Glibenclamide and TEA on EFS-mediated Nitric oxide (NO)-dependent and -independent contractile responses in rabbit lower esophageal sphincter (LES) [1]. The present study addressed the question of whether potassium channels and NO were involved in the relaxant effects of H2S in rabbit LES.
Method
LES was obtained from thirty-six New Zealand Albino male adult rabbits following euthanasia with ketamine/xylazine (50 mg/kg/5mg/kg, IV). LES
was carefully dissected out and two strips were obtained from each animal. For isometric tension studies, strips were mounted in a 20-ml organ
bath containing Krebs solution, which was bubbled with 95% O2 and 5% CO2 and maintained at 37◦C with a pH of 7.4. EFS was applied 16 Hz.,
60 V, 1 ms., 10 s. A tension of 1 g was applied, and tissues were allowed to equilibrate for 1 hour. Effective concentrations of H2S were based on
our preliminary studies [2]. Our experimental protocols are presented inTable 1.
Results
NaHS, L-Cysteine, PAG, and AOAA significantly reduced EFS-mediated NO-dependent and -independent contractile responses. The relaxation
responses significantly varied between the NO-dependent and NO-independent groups (Table 1,2,3,4). NaHS caused statistically significant relaxation meanwhile L-Cysteine and PAG and AOAA did not induce significant relaxation in tissues contracted with KCl and Ca2+. Statistical comparison between the groups was performed by the Kruskal–Wallis test followed by Mann–Whitney U test.
Conclusions
These results suggested that the relaxing effects of hydrogen sulfide on EFS-mediated cholinergic contractile responses may be mediated by nitric
oxide and potassium channels, specifically KV channels in the lower esophageal sphincter.