Coronaridine congeners induce sedative and anxiolytic-like activity in naïve and stressed/anxious mice by allosteric mechanisms involving increased GABAA receptor affinity for GABA
Author:
Funder
Center for Health Sciences, Oklahoma State University
Office of the Vice President for Research, University of Minnesota
Vienna Science and Technology Fund
Publisher
Elsevier BV
Subject
Pharmacology
Reference34 articles.
1. A possible mechanism for anxiolytic and antidepressant effects of alpha- and beta-amyrin from Protium heptaphyllum (Aubl.) March;Aragão;Pharmacol. Biochem. Behav.,2006
2. (+)-Catharanthine potentiates the GABA(A) receptor by binding to a transmembrane site at the β(+)/α(-) interface near the TM2-TM3 loop;Arias;Biochem. Pharmacol.,2022
3. (+)-Catharanthine and (-)-18-methoxycoronaridine induce antidepressant-like activity in mice by differently recruiting serotonergic and norepinephrinergic neurotransmission;Arias;Eur. J. Pharmacol.,2023
4. (+)-Catharanthine and (-)-18-methoxycoronaridine induce antidepressant-like activity in mice by differently recruiting serotonergic and norepinephrinergic neurotransmission;Arias;Eur. J. Pharmacol.,2023
5. Coronaridine congeners potentiate GABA(A) receptors and induce sedative activity in mice in a benzodiazepine-insensitive manner;Arias;Prog. Neuro-Psychopharmacol. Biol. Psychiatry,2020
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. ANXIOLYTICS: Origins, drug discovery, and mechanisms;Pharmacology Biochemistry and Behavior;2024-12
2. GABAergic implications in anxiety and related disorders;Biochemical and Biophysical Research Communications;2024-09
3. Tabernanthalog and ibogainalog inhibit the α7 and α9α10 nicotinic acetylcholine receptors via different mechanisms and with higher potency than the GABAA receptor and CaV2.2 channel;Biochemical Pharmacology;2024-05
4. The novel non-hallucinogenic compound DM506 (3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole) induces sedative- and anxiolytic-like activity in mice by a mechanism involving 5-HT2A receptor activation;European Journal of Pharmacology;2024-03
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3