The additive effect between citalopram and muscimol upon induction of antinociceptive effect in male mice

IF 2 Q3 NEUROSCIENCES
Taha Shokrnejad-namin , Elnaz Amini , Fatemeh Khakpai , Mohammad-Reza Zarrindast
{"title":"The additive effect between citalopram and muscimol upon induction of antinociceptive effect in male mice","authors":"Taha Shokrnejad-namin ,&nbsp;Elnaz Amini ,&nbsp;Fatemeh Khakpai ,&nbsp;Mohammad-Reza Zarrindast","doi":"10.1016/j.ibneur.2024.05.003","DOIUrl":null,"url":null,"abstract":"<div><p>Previous investigations have revealed the role of GABAergic and serotonergic systems in the modulation of pain behavior. This research aimed to examine the effects of intracerebroventricular (i.c.v.) infusion of GABA<sub>A</sub> receptor agonist and antagonist as well as citalopram on pain behavior in male mice. For i.c.v. microinjection, a guide cannula was surgically implanted in the left lateral ventricle of male mice. Pain behavior was evaluated using a tail-flick test. Tail flick latency was measured in each experimental group of mice every 15 min (for 60 min). I.c.v. microinjection of muscimol (0.5 and 1 µg/mouse; GABA<sub>A</sub> receptor agonist) into the left lateral ventricle dose-dependently induced an antinociceptive effect. On the other hand, i.c.v. infusion of bicuculline (1 µg/mouse; GABA<sub>A</sub> receptor antagonist) induced a hyperalgesia response. Moreover, intraperitoneally (i.p.) administration of citalopram (8 mg/kg) produced an antinociceptive effect. Co-treatment of citalopram (8 mg/kg) along with muscimol (0.25 µg/mouse) or bicuculline (0.25 µg/mouse) potentiated the antinociceptive effect produced by citalopram. We found an additive antinociceptive effect of citalopram and muscimol in male mice. In conclusion, our results suggested an interaction between citalopram and GABAergic agents on the modulation of pain behavior in male mice.</p></div>","PeriodicalId":13195,"journal":{"name":"IBRO Neuroscience Reports","volume":null,"pages":null},"PeriodicalIF":2.0000,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667242124000472/pdfft?md5=2e897424261be5d41af55ff0dec10a42&pid=1-s2.0-S2667242124000472-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IBRO Neuroscience Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667242124000472","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Previous investigations have revealed the role of GABAergic and serotonergic systems in the modulation of pain behavior. This research aimed to examine the effects of intracerebroventricular (i.c.v.) infusion of GABAA receptor agonist and antagonist as well as citalopram on pain behavior in male mice. For i.c.v. microinjection, a guide cannula was surgically implanted in the left lateral ventricle of male mice. Pain behavior was evaluated using a tail-flick test. Tail flick latency was measured in each experimental group of mice every 15 min (for 60 min). I.c.v. microinjection of muscimol (0.5 and 1 µg/mouse; GABAA receptor agonist) into the left lateral ventricle dose-dependently induced an antinociceptive effect. On the other hand, i.c.v. infusion of bicuculline (1 µg/mouse; GABAA receptor antagonist) induced a hyperalgesia response. Moreover, intraperitoneally (i.p.) administration of citalopram (8 mg/kg) produced an antinociceptive effect. Co-treatment of citalopram (8 mg/kg) along with muscimol (0.25 µg/mouse) or bicuculline (0.25 µg/mouse) potentiated the antinociceptive effect produced by citalopram. We found an additive antinociceptive effect of citalopram and muscimol in male mice. In conclusion, our results suggested an interaction between citalopram and GABAergic agents on the modulation of pain behavior in male mice.

西酞普兰和麝香草酚在诱导雄性小鼠抗痛觉作用时的相加效应
以往的研究揭示了 GABA 能和血清素能系统在疼痛行为调节中的作用。本研究旨在探讨脑室内注射GABAA受体激动剂和拮抗剂以及西酞普兰对雄性小鼠疼痛行为的影响。在进行 i.c.v. 显微注射时,通过手术将导管植入雄性小鼠的左外侧脑室。疼痛行为通过弹尾试验进行评估。每组小鼠每 15 分钟(60 分钟)测量一次弹尾潜伏期。向左侧脑室静注麝香草酚(0.5 和 1 µg/只小鼠;GABAA 受体激动剂)可产生剂量依赖性的抗痛觉效应。另一方面,静脉注射比库库林(1微克/只小鼠;GABAA受体拮抗剂)会引起痛觉减退反应。此外,腹腔注射(i.p.)西酞普兰(8 毫克/千克)可产生抗痛觉作用。同时服用西酞普兰(8 毫克/千克)和麝香草酚(0.25 微克/只小鼠)或双桉碱(0.25 微克/只小鼠)可增强西酞普兰产生的抗痛觉作用。我们发现,西酞普兰和麝香草酚对雄性小鼠的抗痛觉作用是相加的。总之,我们的研究结果表明,西酞普兰和 GABA 能药物对雄性小鼠疼痛行为的调节具有相互作用。
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
IBRO Neuroscience Reports
IBRO Neuroscience Reports Neuroscience-Neuroscience (all)
CiteScore
2.80
自引率
0.00%
发文量
99
审稿时长
14 weeks
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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