• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

盐酸芬氟拉明治疗帕金森病。

Fenfluramine hydrochloride treatment of parkinsonism.

作者信息

Beasley B L, Davenport R W, Chase T N

出版信息

Arch Neurol. 1977 Apr;34(4):255-6. doi: 10.1001/archneur.1977.00500160069016.

DOI:10.1001/archneur.1977.00500160069016
PMID:843263
Abstract

The oral administration of fenfluramine hydrochloride, which acts centrally to augment serotonin-mediated synaptic function, did not alter extrapyramidal signs in either untreated or levodopa-treated parkinsolian patients. These results support the contention that biochemical indices of serotonergic dysfunction in Parkinson disease do not reflect a critical role for serotonin-containing neural systems in the pathophysiology of parkinsonism and that serotonin-active drugs afford no significant therapeutic benefit to patients with this disorder.

摘要

口服盐酸芬氟拉明,其作用于中枢以增强5-羟色胺介导的突触功能,在未治疗的或左旋多巴治疗的帕金森病患者中均未改变锥体外系体征。这些结果支持以下观点:帕金森病中5-羟色胺能功能障碍的生化指标并不反映含5-羟色胺的神经系统在帕金森病病理生理学中的关键作用,并且5-羟色胺活性药物对患有这种疾病的患者没有显著的治疗益处。

相似文献

1
Fenfluramine hydrochloride treatment of parkinsonism.盐酸芬氟拉明治疗帕金森病。
Arch Neurol. 1977 Apr;34(4):255-6. doi: 10.1001/archneur.1977.00500160069016.
2
Fenfluramine and Parkinson's disease.芬氟拉明与帕金森病
Arch Neurol. 1977 Nov;34(11):720. doi: 10.1001/archneur.1977.00500230090018.
3
[Regulation of food intake and the treatment of obesity using centrally-active serotonergic drugs].[食物摄入的调节及使用中枢活性5-羟色胺能药物治疗肥胖症]
Ned Tijdschr Geneeskd. 1991 Apr 20;135(16):700-3.
4
Serotonergic neurotransmission in early Parkinson's disease: a pilot study to assess implications for depression in this disorder.早期帕金森病中的 5-羟色胺能神经传递:一项评估该疾病中抑郁影响的初步研究。
World J Biol Psychiatry. 2010 Sep;11(6):781-7. doi: 10.3109/15622975.2010.491127.
5
Serotonergic function in obsessive-compulsive disorder. Behavioral and neuroendocrine responses to oral m-chlorophenylpiperazine and fenfluramine in patients and healthy volunteers.
Arch Gen Psychiatry. 1992 Jan;49(1):21-8. doi: 10.1001/archpsyc.1992.01820010021003.
6
[Correlation of clinico-physiologic indices and the serotonin content of the blood of patients with parkinsonism].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1988;88(10):50-2.
7
Interaction between bromocriptine and levodopa. Biochemical basis for an improved treatment for parkinsonism.溴隐亭与左旋多巴的相互作用。帕金森病改善治疗的生化基础。
Neurology. 1977 Jun;27(6):503-10.
8
Blood serotonin concentrations and fenfluramine therapy in autistic children.自闭症儿童的血液血清素浓度与芬氟拉明疗法
J Pediatr. 1986 Mar;108(3):465-9. doi: 10.1016/s0022-3476(86)80903-9.
9
Fenfluramine and dextroamphetamine treatment of childhood hyperactivity. Clinical and biochemical findings.氟苯丙胺和右旋苯丙胺治疗儿童多动症。临床及生化研究结果。
Arch Gen Psychiatry. 1989 Mar;46(3):205-12. doi: 10.1001/archpsyc.1989.01810030011002.
10
Fenfluramine augmentation of serotonin reuptake blockade antiobsessional treatment.氟苯丙胺增强5-羟色胺再摄取阻断抗强迫治疗。
J Clin Psychiatry. 1990 Mar;51(3):119-23.

引用本文的文献

1
Monoamine reuptake inhibitors in Parkinson's disease.单胺再摄取抑制剂在帕金森病中的应用。
Parkinsons Dis. 2015;2015:609428. doi: 10.1155/2015/609428. Epub 2015 Feb 25.
2
Serotonergic mechanisms in Parkinson's disease: opposing results from preclinical and clinical data.帕金森病中的5-羟色胺能机制:临床前和临床数据的相反结果
J Neural Transm (Vienna). 2006 Jan;113(1):59-73. doi: 10.1007/s00702-005-0368-3. Epub 2005 Oct 27.
3
Noradrenaline and 5-hydroxytryptamine modulation of brain dopamine function: implications for the treatment of Parkinson's disease.
去甲肾上腺素和5-羟色胺对脑多巴胺功能的调节:对帕金森病治疗的意义。
Br J Clin Pharmacol. 1983;15 Suppl 2(Suppl 2):277S-289S. doi: 10.1111/j.1365-2125.1983.tb05876.x.
4
Aetiology and natural history of Parkinson's disease.帕金森病的病因及自然史。
Br Med J. 1978 Dec 16;2(6153):1664-6. doi: 10.1136/bmj.2.6153.1664-a.