D. M. Sorokina, I. F. Shaidullov, D. Buchareb, F. G. Sitdikov, G. F. Sitdikova
{"title":"硫化氢对大鼠空肠自发收缩的影响:KV、KCa 和 Kir 通道的作用","authors":"D. M. Sorokina, I. F. Shaidullov, D. Buchareb, F. G. Sitdikov, G. F. Sitdikova","doi":"10.1134/S1990747823060089","DOIUrl":null,"url":null,"abstract":"<p>In this study we investigated the role of voltage dependent (K<sub>V</sub>), Ca<sup>2+</sup>-activated (K<sub>Ca</sub>), and inward rectifier (K<sub>ir</sub>) potassium channels in the effects of hydrogen sulfide donor (H<sub>2</sub>S) sodium hydrosulfide (NaHS) on spontaneous contractile activity of rat jejunum. It was shown that NaHS dose-dependently (10–500 μM) reduced the tonus of the preparation, as well as the amplitude and frequency of spontaneous contractions of jejunum preparations under isometric conditions; the half-maximal effective concentration (EC<sub>50</sub>) of the inhibitory effect of NaHS on the amplitude of contractions was 165 μM. The blocker of K<sub>V</sub> channels 4-AP (200 μM) caused an increase in the amplitude of spontaneous contractions. NaHS (200 μM) decreased the amplitude and frequency of spontaneous activity of the preparation in the presence of 4-AP as well as in the control, and the effect on basal tonus was less pronounced. Blockers of large conductance K<sub>Ca</sub> channels (BK), non-specific TEA (3 mM) and specific paxillin (1 μM), increased the amplitude of spontaneous contractions, while the depressing effect of NaHS was completely preserved. The selective blocker of small conductance K<sub>Ca</sub> channels (SK) NS8593 (4 μM) did not affect the tonus of the preparation and the parameters of spontaneous contractions; it did not prevent the effect of NaHS. The activator of K<sub>ATP</sub> channels diazoxide (100 μM) caused a decrease in the basal tonus of the preparation, as well as the amplitude and frequency of spontaneous contractions. Diazoxide and the K<sub>ATP</sub> channel blocker glibenclamide (50 μM) prevented the effect of NaHS on the tonus of the preparation. BaCl<sub>2</sub>, the K<sub>ir</sub> channel blocker (30 μM), caused an increase in the amplitude of spontaneous contractions and prevented the development of the NaHS inhibitory effects on the frequency and amplitude of spontaneous contractions; the decrease in tonus was less pronounced than in the control. Thus, a decrease in the basal tonus of the rat jejunum preparation under the action of the H<sub>2</sub>S donor was associated with activation of K<sub>ir</sub> channels, including K<sub>ATP</sub> channels, whereas the effect of H<sub>2</sub>S on amplitude and frequency was mediated by an increase in Ba<sup>2+</sup>-sensitive conductivity.</p>","PeriodicalId":484,"journal":{"name":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","volume":"17 4","pages":"301 - 310"},"PeriodicalIF":1.1000,"publicationDate":"2023-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of Hydrogen Sulphide on Spontaneous Contractions of the Rat Jejunum: Role of KV, KCa, and Kir Channels\",\"authors\":\"D. M. Sorokina, I. F. Shaidullov, D. Buchareb, F. G. Sitdikov, G. F. Sitdikova\",\"doi\":\"10.1134/S1990747823060089\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In this study we investigated the role of voltage dependent (K<sub>V</sub>), Ca<sup>2+</sup>-activated (K<sub>Ca</sub>), and inward rectifier (K<sub>ir</sub>) potassium channels in the effects of hydrogen sulfide donor (H<sub>2</sub>S) sodium hydrosulfide (NaHS) on spontaneous contractile activity of rat jejunum. It was shown that NaHS dose-dependently (10–500 μM) reduced the tonus of the preparation, as well as the amplitude and frequency of spontaneous contractions of jejunum preparations under isometric conditions; the half-maximal effective concentration (EC<sub>50</sub>) of the inhibitory effect of NaHS on the amplitude of contractions was 165 μM. The blocker of K<sub>V</sub> channels 4-AP (200 μM) caused an increase in the amplitude of spontaneous contractions. NaHS (200 μM) decreased the amplitude and frequency of spontaneous activity of the preparation in the presence of 4-AP as well as in the control, and the effect on basal tonus was less pronounced. Blockers of large conductance K<sub>Ca</sub> channels (BK), non-specific TEA (3 mM) and specific paxillin (1 μM), increased the amplitude of spontaneous contractions, while the depressing effect of NaHS was completely preserved. The selective blocker of small conductance K<sub>Ca</sub> channels (SK) NS8593 (4 μM) did not affect the tonus of the preparation and the parameters of spontaneous contractions; it did not prevent the effect of NaHS. The activator of K<sub>ATP</sub> channels diazoxide (100 μM) caused a decrease in the basal tonus of the preparation, as well as the amplitude and frequency of spontaneous contractions. Diazoxide and the K<sub>ATP</sub> channel blocker glibenclamide (50 μM) prevented the effect of NaHS on the tonus of the preparation. BaCl<sub>2</sub>, the K<sub>ir</sub> channel blocker (30 μM), caused an increase in the amplitude of spontaneous contractions and prevented the development of the NaHS inhibitory effects on the frequency and amplitude of spontaneous contractions; the decrease in tonus was less pronounced than in the control. 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Effect of Hydrogen Sulphide on Spontaneous Contractions of the Rat Jejunum: Role of KV, KCa, and Kir Channels
In this study we investigated the role of voltage dependent (KV), Ca2+-activated (KCa), and inward rectifier (Kir) potassium channels in the effects of hydrogen sulfide donor (H2S) sodium hydrosulfide (NaHS) on spontaneous contractile activity of rat jejunum. It was shown that NaHS dose-dependently (10–500 μM) reduced the tonus of the preparation, as well as the amplitude and frequency of spontaneous contractions of jejunum preparations under isometric conditions; the half-maximal effective concentration (EC50) of the inhibitory effect of NaHS on the amplitude of contractions was 165 μM. The blocker of KV channels 4-AP (200 μM) caused an increase in the amplitude of spontaneous contractions. NaHS (200 μM) decreased the amplitude and frequency of spontaneous activity of the preparation in the presence of 4-AP as well as in the control, and the effect on basal tonus was less pronounced. Blockers of large conductance KCa channels (BK), non-specific TEA (3 mM) and specific paxillin (1 μM), increased the amplitude of spontaneous contractions, while the depressing effect of NaHS was completely preserved. The selective blocker of small conductance KCa channels (SK) NS8593 (4 μM) did not affect the tonus of the preparation and the parameters of spontaneous contractions; it did not prevent the effect of NaHS. The activator of KATP channels diazoxide (100 μM) caused a decrease in the basal tonus of the preparation, as well as the amplitude and frequency of spontaneous contractions. Diazoxide and the KATP channel blocker glibenclamide (50 μM) prevented the effect of NaHS on the tonus of the preparation. BaCl2, the Kir channel blocker (30 μM), caused an increase in the amplitude of spontaneous contractions and prevented the development of the NaHS inhibitory effects on the frequency and amplitude of spontaneous contractions; the decrease in tonus was less pronounced than in the control. Thus, a decrease in the basal tonus of the rat jejunum preparation under the action of the H2S donor was associated with activation of Kir channels, including KATP channels, whereas the effect of H2S on amplitude and frequency was mediated by an increase in Ba2+-sensitive conductivity.
期刊介绍:
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology is an international peer reviewed journal that publishes original articles on physical, chemical, and molecular mechanisms that underlie basic properties of biological membranes and mediate membrane-related cellular functions. The primary topics of the journal are membrane structure, mechanisms of membrane transport, bioenergetics and photobiology, intracellular signaling as well as membrane aspects of cell biology, immunology, and medicine. The journal is multidisciplinary and gives preference to those articles that employ a variety of experimental approaches, basically in biophysics but also in biochemistry, cytology, and molecular biology. The journal publishes articles that strive for unveiling membrane and cellular functions through innovative theoretical models and computer simulations.