MD-354: What is It Good For?

Małgorzata Dukat, Richard A. Glennon, Shawquia Young
{"title":"MD-354: What is It Good For?","authors":"Małgorzata Dukat,&nbsp;Richard A. Glennon,&nbsp;Shawquia Young","doi":"10.1111/j.1527-3458.2007.00002.x","DOIUrl":null,"url":null,"abstract":"<p>MD-354 (<i>meta</i>-chlorophenylguanidine) has been identified as a member of a novel class of 5-HT<sub>3</sub> serotonin receptor agonists. MD-354 is a 5-HT<sub>3</sub> receptor partial agonist that has been shown to behave as an agonist in some assays, and as an antagonist in others. MD-354 also binds at α-adrenoceptors (ARs) and displays an affinity for α<sub>2B</sub>-ARs comparable to its affinity for 5-HT<sub>3</sub> receptors. Although devoid of antinociceptive actions following systemic administration alone, MD-354 markedly enhances the antinociceptive actions of clonidine in the mouse tail-flick assay without potentiating the sedative side effects of clonidine. Although studies with MD-354 are still in progress, some pharmacological findings are described here. MD-354-related agents may represent drug adjuvants for the relief of severe pain.</p>","PeriodicalId":94307,"journal":{"name":"CNS drug reviews","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2007-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1527-3458.2007.00002.x","citationCount":"16","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CNS drug reviews","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/j.1527-3458.2007.00002.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 16

Abstract

MD-354 (meta-chlorophenylguanidine) has been identified as a member of a novel class of 5-HT3 serotonin receptor agonists. MD-354 is a 5-HT3 receptor partial agonist that has been shown to behave as an agonist in some assays, and as an antagonist in others. MD-354 also binds at α-adrenoceptors (ARs) and displays an affinity for α2B-ARs comparable to its affinity for 5-HT3 receptors. Although devoid of antinociceptive actions following systemic administration alone, MD-354 markedly enhances the antinociceptive actions of clonidine in the mouse tail-flick assay without potentiating the sedative side effects of clonidine. Although studies with MD-354 are still in progress, some pharmacological findings are described here. MD-354-related agents may represent drug adjuvants for the relief of severe pain.

Abstract Image

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
MD-354:它有什么用?
MD-354(间氯苯胍)已被确定为一类新的5-HT3血清素受体激动剂的成员。MD-354是一种5-HT3受体部分激动剂,在一些试验中表现为激动剂,在另一些试验中表现为拮抗剂。MD-354也与α-肾上腺素受体(ARs)结合,并表现出与α2B-ARs的亲和力,其与5-HT3受体的亲和力相当。在小鼠摇尾实验中,MD-354虽然在全身单独给药后没有抗痛觉作用,但它能显著增强可乐定的抗痛觉作用,而不会增强可乐定的镇静副作用。虽然对MD-354的研究仍在进行中,但这里描述了一些药理学发现。md -354相关药物可能是缓解剧烈疼痛的药物佐剂。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
ERRATUM Cortagine: Behavioral and Autonomic Function of the Selective CRF Receptor Subtype 1 Agonist Guanfacine and Guanfacine Extended Release: Treatment for ADHD and Related Disorders Pharmacology of the β-Carboline FG-7142, a Partial Inverse Agonist at the Benzodiazepine Allosteric Site of the GABAA Receptor: Neurochemical, Neurophysiological, and Behavioral Effects AUTHOR INDEX FOR VOLUME 13
×
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