DIFFERENTIAL RESPONSES TO PROSTAGLANDINS IN THE CIRCULAR AND LONGITUDINAL MUSCLE LAYERS OF THE MURINE ILEUM.

IF 3.9 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Joong Goo Kwon, Sung Jin Hwang, Elizabeth A H Beckett, Kenton M Sanders, Sean Ward
{"title":"DIFFERENTIAL RESPONSES TO PROSTAGLANDINS IN THE CIRCULAR AND LONGITUDINAL MUSCLE LAYERS OF THE MURINE ILEUM.","authors":"Joong Goo Kwon, Sung Jin Hwang, Elizabeth A H Beckett, Kenton M Sanders, Sean Ward","doi":"10.1152/ajpgi.00400.2024","DOIUrl":null,"url":null,"abstract":"<p><p>Prostaglandin E<sub>2</sub> (PGE<sub>2</sub>) actions on intestinal motility are complex due the differential expression of the PGE<sub>2</sub> receptors EP1-EP4. We sought to determine the actions of PGE<sub>2</sub> on electrical pacemaker and contractile activity of the circular and longitudinal muscle layers of the murine small intestine. Intracellular microelectrode and isometric force measurements were performed to examine the effects of PGE<sub>2</sub> receptor activation on circular and longitudinal muscle layers. In the two muscle layers PGE<sub>2</sub> produced differential responses. In the circular muscle layer PGE<sub>2</sub> caused dose-dependent membrane hyperpolarization and reduction in slow wave amplitude, accompanied by a decrease in the amplitude of phasic contractions. Membrane hyperpolarization and the reduction in slow wave amplitude and phasic contractions were insensitive to TTX and L-NNA, but inhibited by the K<sub>ATP</sub> channel antagonist, glibenclamide. The actions of PGE<sub>2</sub> on the circular muscle layer were mimicked by the selective EP<sub>2</sub> and EP<sub>4</sub> agonists ONO AE1-259 and ONO AE1-329, respectively. The actions of PGE<sub>2</sub> were partially inhibited by the EP4 antagonist ONO AE3-208. The EP<sub>1</sub> agonist ONO DI-004 produced little effect while the EP3 agonist ONO AE-248 caused dose-dependent membrane depolarization. In comparison, PGE<sub>2</sub> produced increased tone and phasic contractions in the longitudinal muscle layer that was mimicked by ONO DI-004 and ONO AE-248, while EP<sub>2</sub> and EP<sub>4</sub> agonists had little effect on contractile activity. These data suggest that differential expression of PGE<sub>2</sub> receptors on intestinal muscle layers can produce antagonistic actions on intestinal motility.</p>","PeriodicalId":7725,"journal":{"name":"American journal of physiology. Gastrointestinal and liver physiology","volume":" ","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Gastrointestinal and liver physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpgi.00400.2024","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Prostaglandin E2 (PGE2) actions on intestinal motility are complex due the differential expression of the PGE2 receptors EP1-EP4. We sought to determine the actions of PGE2 on electrical pacemaker and contractile activity of the circular and longitudinal muscle layers of the murine small intestine. Intracellular microelectrode and isometric force measurements were performed to examine the effects of PGE2 receptor activation on circular and longitudinal muscle layers. In the two muscle layers PGE2 produced differential responses. In the circular muscle layer PGE2 caused dose-dependent membrane hyperpolarization and reduction in slow wave amplitude, accompanied by a decrease in the amplitude of phasic contractions. Membrane hyperpolarization and the reduction in slow wave amplitude and phasic contractions were insensitive to TTX and L-NNA, but inhibited by the KATP channel antagonist, glibenclamide. The actions of PGE2 on the circular muscle layer were mimicked by the selective EP2 and EP4 agonists ONO AE1-259 and ONO AE1-329, respectively. The actions of PGE2 were partially inhibited by the EP4 antagonist ONO AE3-208. The EP1 agonist ONO DI-004 produced little effect while the EP3 agonist ONO AE-248 caused dose-dependent membrane depolarization. In comparison, PGE2 produced increased tone and phasic contractions in the longitudinal muscle layer that was mimicked by ONO DI-004 and ONO AE-248, while EP2 and EP4 agonists had little effect on contractile activity. These data suggest that differential expression of PGE2 receptors on intestinal muscle layers can produce antagonistic actions on intestinal motility.

小鼠回肠环形和纵肌层对前列腺素的不同反应。
前列腺素E2 (PGE2)对肠道蠕动的作用是复杂的,因为PGE2受体EP1-EP4的差异表达。我们试图确定PGE2对电起搏器和小鼠小肠环形和纵向肌肉层收缩活动的作用。通过细胞内微电极和等距力测量来检测PGE2受体激活对圆形和纵向肌肉层的影响。在两个肌肉层中,PGE2产生了不同的反应。在圆形肌层,PGE2引起剂量依赖性膜超极化和慢波振幅降低,同时伴有相收缩幅度的降低。TTX和L-NNA对细胞膜超极化、慢波振幅降低和相性收缩不敏感,但被KATP通道拮抗剂格列本脲抑制。EP2和EP4选择性激动剂ONO AE1-259和ONO AE1-329分别模拟了PGE2对圆形肌层的作用。EP4拮抗剂ONO AE3-208可部分抑制PGE2的作用。EP1激动剂ONO DI-004对膜去极化作用不明显,而EP3激动剂ONO AE-248对膜去极化作用呈剂量依赖性。相比之下,ONO DI-004和ONO AE-248可以增强PGE2在纵肌层的张力和相性收缩,而EP2和EP4激动剂对收缩活性的影响很小。这些数据提示PGE2受体在肠肌层上的差异表达可对肠蠕动产生拮抗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.40
自引率
2.20%
发文量
104
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Gastrointestinal and Liver Physiology publishes original articles pertaining to all aspects of research involving normal or abnormal function of the gastrointestinal tract, hepatobiliary system, and pancreas. Authors are encouraged to submit manuscripts dealing with growth and development, digestion, secretion, absorption, metabolism, and motility relative to these organs, as well as research reports dealing with immune and inflammatory processes and with neural, endocrine, and circulatory control mechanisms that affect these organs.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信