通过小鼠大脑新皮层结合试验评估抗抑郁药对毒蕈碱受体的抑制作用

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of pharmacological sciences Pub Date : 2024-09-11 DOI:10.1016/j.jphs.2024.09.001
Keisuke Obara, Yuki Usami, Risa Okamoto, Kento Yoshioka, Yoshio Tanaka
{"title":"通过小鼠大脑新皮层结合试验评估抗抑郁药对毒蕈碱受体的抑制作用","authors":"Keisuke Obara,&nbsp;Yuki Usami,&nbsp;Risa Okamoto,&nbsp;Kento Yoshioka,&nbsp;Yoshio Tanaka","doi":"10.1016/j.jphs.2024.09.001","DOIUrl":null,"url":null,"abstract":"<div><div>We investigated the inhibitory effects of 32 antidepressants on [<sup>3</sup>H]<em>N</em>-methylscopolamine ([<sup>3</sup>H]NMS)-specific binding in the mouse cerebral neocortex to determine which antidepressants should be recommended for patients with Alzheimer's disease (AD). Of those tested, nine antidepressants (10<sup>−4</sup> M) exhibited less inhibitory effect on [<sup>3</sup>H]NMS-specific binding (&lt;35%): tianeptine (a tricyclic); trazodone (a serotonin 5-HT<sub>2A</sub> blocker); sulpiride (a dopamine D<sub>2</sub> blocker); fluvoxamine (a selective serotonin reuptake inhibitor (RI)); milnacipran, levomilnacipran, venlafaxine, and desvenlafaxine (serotonin and noradrenaline RIs); and bupropion (a noradrenaline and dopamine RI). Therefore, these antidepressants show little anticholinergic effect in the brain and are recommended for use in patients with AD.</div></div>","PeriodicalId":16786,"journal":{"name":"Journal of pharmacological sciences","volume":"156 4","pages":"Pages 214-217"},"PeriodicalIF":3.0000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of inhibitory actions of antidepressants on muscarinic receptors assessed by a binding assay in the mouse cerebral neocortex\",\"authors\":\"Keisuke Obara,&nbsp;Yuki Usami,&nbsp;Risa Okamoto,&nbsp;Kento Yoshioka,&nbsp;Yoshio Tanaka\",\"doi\":\"10.1016/j.jphs.2024.09.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>We investigated the inhibitory effects of 32 antidepressants on [<sup>3</sup>H]<em>N</em>-methylscopolamine ([<sup>3</sup>H]NMS)-specific binding in the mouse cerebral neocortex to determine which antidepressants should be recommended for patients with Alzheimer's disease (AD). Of those tested, nine antidepressants (10<sup>−4</sup> M) exhibited less inhibitory effect on [<sup>3</sup>H]NMS-specific binding (&lt;35%): tianeptine (a tricyclic); trazodone (a serotonin 5-HT<sub>2A</sub> blocker); sulpiride (a dopamine D<sub>2</sub> blocker); fluvoxamine (a selective serotonin reuptake inhibitor (RI)); milnacipran, levomilnacipran, venlafaxine, and desvenlafaxine (serotonin and noradrenaline RIs); and bupropion (a noradrenaline and dopamine RI). Therefore, these antidepressants show little anticholinergic effect in the brain and are recommended for use in patients with AD.</div></div>\",\"PeriodicalId\":16786,\"journal\":{\"name\":\"Journal of pharmacological sciences\",\"volume\":\"156 4\",\"pages\":\"Pages 214-217\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pharmacological sciences\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1347861324000641\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmacological sciences","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1347861324000641","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

我们研究了32种抗抑郁药对小鼠大脑新皮层中[3H]N-甲基东莨菪碱([3H]NMS)特异性结合的抑制作用,以确定哪些抗抑郁药应推荐给阿尔茨海默病患者(AD)。在接受测试的药物中,有九种抗抑郁药(10-4 M)对[3H]NMS特异性结合的抑制作用较小(35%):噻奈普汀(一种三环类药物);曲唑酮(一种血清素 5-HT2A 阻断剂);舒必利(一种多巴胺 D2 阻断剂);氟伏沙明(一种选择性血清素再摄取抑制剂 (RI));米那西普兰、左米那西普兰、文拉法辛和去文拉法辛(血清素和去甲肾上腺素 RI);以及安非他酮(一种去甲肾上腺素和多巴胺 RI)。因此,这些抗抑郁药对大脑的抗胆碱能作用很小,建议用于注意力缺失症患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Evaluation of inhibitory actions of antidepressants on muscarinic receptors assessed by a binding assay in the mouse cerebral neocortex
We investigated the inhibitory effects of 32 antidepressants on [3H]N-methylscopolamine ([3H]NMS)-specific binding in the mouse cerebral neocortex to determine which antidepressants should be recommended for patients with Alzheimer's disease (AD). Of those tested, nine antidepressants (10−4 M) exhibited less inhibitory effect on [3H]NMS-specific binding (<35%): tianeptine (a tricyclic); trazodone (a serotonin 5-HT2A blocker); sulpiride (a dopamine D2 blocker); fluvoxamine (a selective serotonin reuptake inhibitor (RI)); milnacipran, levomilnacipran, venlafaxine, and desvenlafaxine (serotonin and noradrenaline RIs); and bupropion (a noradrenaline and dopamine RI). Therefore, these antidepressants show little anticholinergic effect in the brain and are recommended for use in patients with AD.
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
6.20
自引率
2.90%
发文量
104
审稿时长
31 days
期刊介绍: Journal of Pharmacological Sciences (JPS) is an international open access journal intended for the advancement of pharmacological sciences in the world. The Journal welcomes submissions in all fields of experimental and clinical pharmacology, including neuroscience, and biochemical, cellular, and molecular pharmacology for publication as Reviews, Full Papers or Short Communications. Short Communications are short research article intended to provide novel and exciting pharmacological findings. Manuscripts concerning descriptive case reports, pharmacokinetic and pharmacodynamic studies without pharmacological mechanism and dose-response determinations are not acceptable and will be rejected without peer review. The ethnopharmacological studies are also out of the scope of this journal. Furthermore, JPS does not publish work on the actions of biological extracts unknown chemical composition.
期刊最新文献
Rehmannioside A promotes the osteoblastic differentiation of MC3T3-E1 cells via the PI3K/AKT signaling pathway and inhibits glucocorticoid-induced bone loss in vivo Targeting TMEM16A ion channels suppresses airway hyperreactivity, inflammation, and remodeling in an experimental Guinea pig asthma model Glucosylceramide synthase inhibitor ameliorates chronic inflammatory pain TND1128, a 5-deazaflavin derivative with auto-redox ability, facilitates polarization of mitochondrial membrane potential (ΔΨm) and on-demand ATP synthesis in mice brain slices Analgesic effect of Keishinieppiittokajutsubu on low barometric pressure-induced pain response in arthritic model rats
×
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