硫化氢对大鼠空肠自发收缩的影响:KV、KCa 和 Kir 通道的作用

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,&nbsp;I. F. Shaidullov,&nbsp;D. Buchareb,&nbsp;F. G. Sitdikov,&nbsp;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":null,"pages":null},"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,&nbsp;I. F. Shaidullov,&nbsp;D. Buchareb,&nbsp;F. G. Sitdikov,&nbsp;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\":null,\"pages\":null},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2023-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1990747823060089\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology","FirstCategoryId":"2","ListUrlMain":"https://link.springer.com/article/10.1134/S1990747823060089","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

本研究探讨了硫化氢供体(H2S)硫氢化钠(NaHS)对大鼠空肠自发收缩活动的影响中电压依赖性(KV)、Ca2+激活(KCa)和内向整流(Kir)钾通道的作用。研究表明,NaHS 可剂量依赖性地(10-500 μM)降低空肠制备物的张力,以及等长条件下空肠制备物自发收缩的幅度和频率;NaHS 对收缩幅度抑制作用的半最大有效浓度(EC50)为 165 μM。KV 通道阻断剂 4-AP(200 μM)会导致自发收缩幅度增加。NaHS(200 μM)可降低制备物在 4-AP 存在下的自发活动幅度和频率,与对照组相同,但对基础张力的影响不明显。大电导 KCa 通道(BK)阻断剂、非特异性 TEA(3 mM)和特异性 paxillin(1 μM)增加了自发收缩的幅度,而 NaHS 的抑制作用则完全保留。小电导 KCa 通道(SK)选择性阻断剂 NS8593(4 μM)不影响制备物的张力和自发收缩的参数,也不能阻止 NaHS 的作用。KATP 通道激活剂二氮氧化物(100 μM)导致制备物的基础张力以及自发收缩的幅度和频率下降。重氮氧化物和 KATP 通道阻断剂格列本脲(50 μM)可防止 NaHS 对制备物的张力产生影响。Kir通道阻断剂BaCl2(30 μM)会导致自发收缩幅度的增加,并阻止NaHS对自发收缩频率和幅度的抑制作用的发展;与对照组相比,强直性的下降并不那么明显。因此,在 H2S 供体的作用下,大鼠空肠制备的基础张力下降与 Kir 通道(包括 KATP 通道)的激活有关,而 H2S 对振幅和频率的影响是由 Ba2+ 敏感传导性的增加介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
1.40
自引率
0.00%
发文量
28
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.
期刊最新文献
The Rhodopsin Project To the 90th Anniversary of the Birth of Academician Yuri Anatolievich Ovchinnikov Alterations of Store-Operated Calcium Entry in Neurodegenerative Pathologies: History, Facts, and Prospects Structural Studies of Ion Channels: Achievements, Problems, and Perspectives Structure and Functions of the OTOP1 Proton Channel
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1