氯胺酮快速缓解抑郁:探索复杂的作用机制

K. Blum, T. Pappas, B. Clifton, D. Baron, Margaret A. Madigan, L. Lott, M. Moran, C. Clifton, Scott Worrich, E. Clarke, B. Boyett, A. Bowirrat, M. Gold
{"title":"氯胺酮快速缓解抑郁:探索复杂的作用机制","authors":"K. Blum, T. Pappas, B. Clifton, D. Baron, Margaret A. Madigan, L. Lott, M. Moran, C. Clifton, Scott Worrich, E. Clarke, B. Boyett, A. Bowirrat, M. Gold","doi":"10.2174/2211556008666190827150018","DOIUrl":null,"url":null,"abstract":"\n\nSuicide rates and narcotic overdose have doubled since 2000.\nAt least 30 percent of people with major depression are Treatment-Resistant (TR) and\nrequire novel therapeutics. ketamine at low doses has been shown in clinical trials to\ninduce a rapid, short-lived anti-suicide and anti-depressant effect.\n\n\n\nTo review the potential mechanism of action of ketamines’ alleviation of\ndepressive symptoms from both animal and available human literature.\n\n\n\nThis is a synthesis of information from papers listed in PUBMED Central.\nAlthough not exhaustive, this review highlights the most compelling work in the field\nrelated to this remarkable clinical rapid anti-depressant effect.\n\n\n\nWhile there have been several theories and with some scientific evidence to\ndate, the conclusion here is that currently, an exact and acceptable mechanism of\naction (MOA) for ketamines’ rapid anti-depressant effect is not apparent. The MOA of\nthis compound with psychoactive abuse potential at a higher dosage and acute antidepressive\neffect in the most resistant patients is unknown.\n\n\n\nPossible MOAs reviewed, include dopamine receptor modulation through\nepigenetic neuroadaptation via specific D1/D2 antagonism, D1 activation using optogenetic\nstimulation, and the role of D2/D3 availability in the ketamine therapeutic action.\n\n\n\nUnraveling MOA could guide the development of other unique Psychoplastogens\ncapable of rapidly promoting structural and functional neural plasticity in\ncases of TR Major Depressive Episodes (MDE) and unipolar Major Depression Disorder\n(MDD).\n","PeriodicalId":10751,"journal":{"name":"Current Psychopharmacology","volume":"15 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Rapid Anti-Depressant Relief by Ketamine: Exploring A Complex Mechanism of Action\",\"authors\":\"K. Blum, T. Pappas, B. Clifton, D. Baron, Margaret A. Madigan, L. Lott, M. Moran, C. Clifton, Scott Worrich, E. Clarke, B. Boyett, A. Bowirrat, M. Gold\",\"doi\":\"10.2174/2211556008666190827150018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nSuicide rates and narcotic overdose have doubled since 2000.\\nAt least 30 percent of people with major depression are Treatment-Resistant (TR) and\\nrequire novel therapeutics. ketamine at low doses has been shown in clinical trials to\\ninduce a rapid, short-lived anti-suicide and anti-depressant effect.\\n\\n\\n\\nTo review the potential mechanism of action of ketamines’ alleviation of\\ndepressive symptoms from both animal and available human literature.\\n\\n\\n\\nThis is a synthesis of information from papers listed in PUBMED Central.\\nAlthough not exhaustive, this review highlights the most compelling work in the field\\nrelated to this remarkable clinical rapid anti-depressant effect.\\n\\n\\n\\nWhile there have been several theories and with some scientific evidence to\\ndate, the conclusion here is that currently, an exact and acceptable mechanism of\\naction (MOA) for ketamines’ rapid anti-depressant effect is not apparent. The MOA of\\nthis compound with psychoactive abuse potential at a higher dosage and acute antidepressive\\neffect in the most resistant patients is unknown.\\n\\n\\n\\nPossible MOAs reviewed, include dopamine receptor modulation through\\nepigenetic neuroadaptation via specific D1/D2 antagonism, D1 activation using optogenetic\\nstimulation, and the role of D2/D3 availability in the ketamine therapeutic action.\\n\\n\\n\\nUnraveling MOA could guide the development of other unique Psychoplastogens\\ncapable of rapidly promoting structural and functional neural plasticity in\\ncases of TR Major Depressive Episodes (MDE) and unipolar Major Depression Disorder\\n(MDD).\\n\",\"PeriodicalId\":10751,\"journal\":{\"name\":\"Current Psychopharmacology\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-10-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Psychopharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2211556008666190827150018\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Psychopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2211556008666190827150018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

自2000年以来,自杀率和吸毒过量增加了一倍。至少30%的重度抑郁症患者有治疗耐药性,需要新的治疗方法。临床试验显示,低剂量氯胺酮可产生快速、短期的抗自杀和抗抑郁效果。从动物和人类文献中回顾氯胺酮缓解抑郁症状的潜在作用机制。这是PUBMED Central中列出的论文信息的综合。虽然不是详尽的,但这篇综述强调了与这种显著的临床快速抗抑郁作用相关的领域中最引人注目的工作。虽然目前有几种理论和一些科学证据,但这里的结论是,目前,氯胺酮快速抗抑郁作用的确切和可接受的机制(MOA)尚不明显。这种化合物在高剂量时具有精神活性滥用的可能性,在最耐药的患者中具有急性抗抑郁作用,其MOA未知。综述了可能的MOAs,包括通过特异性D1/D2拮抗剂通过遗传神经适应调节多巴胺受体,利用光遗传刺激激活D1,以及D2/D3可用性在氯胺酮治疗作用中的作用。揭示MOA可以指导其他独特的心理成因的发展,这些心理成因能够快速促进TR型重度抑郁发作(MDE)和单极型重度抑郁障碍(MDD)患者的结构和功能神经可塑性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid Anti-Depressant Relief by Ketamine: Exploring A Complex Mechanism of Action
Suicide rates and narcotic overdose have doubled since 2000. At least 30 percent of people with major depression are Treatment-Resistant (TR) and require novel therapeutics. ketamine at low doses has been shown in clinical trials to induce a rapid, short-lived anti-suicide and anti-depressant effect. To review the potential mechanism of action of ketamines’ alleviation of depressive symptoms from both animal and available human literature. This is a synthesis of information from papers listed in PUBMED Central. Although not exhaustive, this review highlights the most compelling work in the field related to this remarkable clinical rapid anti-depressant effect. While there have been several theories and with some scientific evidence to date, the conclusion here is that currently, an exact and acceptable mechanism of action (MOA) for ketamines’ rapid anti-depressant effect is not apparent. The MOA of this compound with psychoactive abuse potential at a higher dosage and acute antidepressive effect in the most resistant patients is unknown. Possible MOAs reviewed, include dopamine receptor modulation through epigenetic neuroadaptation via specific D1/D2 antagonism, D1 activation using optogenetic stimulation, and the role of D2/D3 availability in the ketamine therapeutic action. Unraveling MOA could guide the development of other unique Psychoplastogens capable of rapidly promoting structural and functional neural plasticity in cases of TR Major Depressive Episodes (MDE) and unipolar Major Depression Disorder (MDD).
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
自引率
0.00%
发文量
0
×
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