Suppr超能文献

豚鼠脑中右美沙芬结合位点

Dextromethorphan binding sites in the guinea pig brain.

作者信息

Musacchio J M, Klein M

机构信息

Department of Pharmacology, New York University Medical Center, New York 10016.

出版信息

Cell Mol Neurobiol. 1988 Jun;8(2):149-56. doi: 10.1007/BF00711241.

Abstract
  1. Dextromethorphan (DM), a dextrorotatory nonopioid antitussive, binds to specific high-affinity sites in the central nervous system. These sites are distinct from the opioid and other known neurotransmitter receptor sites. Antitussives such as carbetapentane and caramiphen also bind to DM sites with a nanomolar affinity. 2. The anticonvulsant drugs phenytoin and ropizine produce an allosteric enhancement of the binding of [3H]DM to guinea pig brain. DM, carbetapentane, and caramiphen also are efficacious anticonvulsant agents in the rat maximal electroshock seizures test, and DM enhances the anticonvulsant effects of phenytoin (PHT). 3. These results suggest that drugs that bind to the DM sites could be used alone as anticonvulsants or in combination with PHT to lower its effective dose and reduce its side effects. 4. The investigation of the DM binding sites may help to open new approaches for the treatment of convulsive disorders and to explain further some of the molecular mechanisms of neutronal excitability.
摘要
  1. 右美沙芬(DM)是一种右旋非阿片类镇咳药,可与中枢神经系统中的特定高亲和力位点结合。这些位点与阿片类及其他已知神经递质受体位点不同。卡比喷托和卡拉美芬等镇咳药也以纳摩尔亲和力与DM位点结合。2. 抗惊厥药物苯妥英和罗匹嗪可对[3H]DM与豚鼠脑的结合产生变构增强作用。DM、卡比喷托和卡拉美芬在大鼠最大电休克惊厥试验中也是有效的抗惊厥剂,且DM可增强苯妥英(PHT)的抗惊厥作用。3. 这些结果表明,与DM位点结合的药物可单独用作抗惊厥药,或与PHT联合使用以降低其有效剂量并减少其副作用。4. 对DM结合位点的研究可能有助于开辟治疗惊厥性疾病的新方法,并进一步解释神经元兴奋性的一些分子机制。

相似文献

1
Dextromethorphan binding sites in the guinea pig brain.豚鼠脑中右美沙芬结合位点
Cell Mol Neurobiol. 1988 Jun;8(2):149-56. doi: 10.1007/BF00711241.
3
Allosteric modulation of dextromethorphan binding sites.右美沙芬结合位点的变构调节
Neuropharmacology. 1987 Jul;26(7B):997-1001. doi: 10.1016/0028-3908(87)90078-5.

引用本文的文献

2
Sigma-1 receptor and seizures.Sigma-1 受体与癫痫发作。
Pharmacol Res. 2023 May;191:106771. doi: 10.1016/j.phrs.2023.106771. Epub 2023 Apr 15.
3
Repurposing Sigma-1 Receptor Ligands for COVID-19 Therapy?将西格玛-1受体配体重新用于治疗新冠病毒肺炎?
Front Pharmacol. 2020 Nov 9;11:582310. doi: 10.3389/fphar.2020.582310. eCollection 2020.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验