• 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

氟哌啶醇激发试验对精神分裂症反应性和无反应性患者脑区代谢的影响。

Effect of a haloperidol challenge on regional brain metabolism in neuroleptic-responsive and nonresponsive schizophrenic patients.

作者信息

Bartlett E J, Brodie J D, Simkowitz P, Schlösser R, Dewey S L, Lindenmayer J P, Rusinek H, Wolkin A, Cancro R, Schiffer W

机构信息

Department of Psychiatry, New York University Medical Center, NY 10016, USA.

出版信息

Am J Psychiatry. 1998 Mar;155(3):337-43. doi: 10.1176/ajp.155.3.337.

DOI:10.1176/ajp.155.3.337
PMID:9501742
Abstract

OBJECTIVE

The CNS metabolic response to a neuroleptic challenge in treatment-responsive and nonresponsive schizophrenic patients was measured in order to examine the relation between treatment outcome and the capacity to alter neurochemical function in response to acute receptor blockade.

METHOD

Positron emission tomography (PET) and [18F]fluorodeoxyglucose (FDG) were used to measure regional cerebral metabolism in seven schizophrenic patients judged to have been responsive to drug treatment previously and seven nonresponsive schizophrenic patients after a drug-free period of at least 3 weeks (baseline) and again 12 hours after administration of 5.0 mg of haloperidol.

RESULTS

The haloperidol challenge caused widespread decreases in absolute metabolism in the nonresponsive patients but not the responsive patients. These group differences reflect the findings on the second (challenge) scans, since metabolic values at baseline were not statistically different in the two groups. The pattern of decreased metabolic activity in the nonresponders after the haloperidol challenge is similar to that previously observed in normal subjects.

CONCLUSIONS

The metabolic response to drug challenge separates treatment responders from nonresponders and normal subjects. The results suggest that subtyping of schizophrenia (and other psychiatric disorders) can be achieved by measuring the physiologic response to a pharmacologic challenge in vivo with chemical brain-imaging techniques.

摘要

目的

测量治疗反应性和无反应性精神分裂症患者对神经阻滞剂激发试验的中枢神经系统代谢反应,以研究治疗结果与急性受体阻断后改变神经化学功能能力之间的关系。

方法

使用正电子发射断层扫描(PET)和[18F]氟脱氧葡萄糖(FDG)测量7名先前被判定对药物治疗有反应的精神分裂症患者和7名无反应性精神分裂症患者在至少3周的无药期(基线)以及给予5.0毫克氟哌啶醇12小时后的局部脑代谢。

结果

氟哌啶醇激发试验导致无反应性患者的绝对代谢普遍降低,但反应性患者未出现这种情况。这些组间差异反映了第二次(激发)扫描的结果,因为两组基线时的代谢值无统计学差异。氟哌啶醇激发试验后无反应者代谢活性降低的模式与先前在正常受试者中观察到的相似。

结论

对药物激发试验的代谢反应可区分治疗反应者与无反应者及正常受试者。结果表明,通过用化学脑成像技术在体内测量对药物激发试验的生理反应,可以实现精神分裂症(及其他精神障碍)的亚型分类。

相似文献

1
Effect of a haloperidol challenge on regional brain metabolism in neuroleptic-responsive and nonresponsive schizophrenic patients.氟哌啶醇激发试验对精神分裂症反应性和无反应性患者脑区代谢的影响。
Am J Psychiatry. 1998 Mar;155(3):337-43. doi: 10.1176/ajp.155.3.337.
2
Functional sites of neuroleptic drug action in the human brain: PET/FDG studies with and without haloperidol.抗精神病药物在人脑中的作用功能位点:使用和不使用氟哌啶醇的PET/FDG研究
Am J Psychiatry. 1996 Jan;153(1):41-9. doi: 10.1176/ajp.153.1.41.
3
Blunted change in cerebral glucose utilization after haloperidol treatment in schizophrenic patients with prominent negative symptoms.在具有显著阴性症状的精神分裂症患者中,氟哌啶醇治疗后脑葡萄糖利用变化减弱。
Am J Psychiatry. 1996 Mar;153(3):346-54. doi: 10.1176/ajp.153.3.346.
4
Effects of haloperidol challenge on regional cerebral glucose utilization in normal human subjects.氟哌啶醇激发试验对正常人体受试者局部脑葡萄糖利用的影响。
Am J Psychiatry. 1994 May;151(5):681-6. doi: 10.1176/ajp.151.5.681.
5
High levels of dopamine D2 receptor occupancy with low-dose haloperidol treatment: a PET study.
Am J Psychiatry. 1996 Jul;153(7):948-50. doi: 10.1176/ajp.153.7.948.
6
D2 dopamine receptor occupancy during low-dose treatment with haloperidol decanoate.癸酸氟哌啶醇低剂量治疗期间的D2多巴胺受体占有率。
Am J Psychiatry. 1995 Feb;152(2):173-8. doi: 10.1176/ajp.152.2.173.
7
Effects of methylphenidate on regional brain glucose metabolism in humans: relationship to dopamine D2 receptors.哌甲酯对人类大脑局部葡萄糖代谢的影响:与多巴胺D2受体的关系。
Am J Psychiatry. 1997 Jan;154(1):50-5. doi: 10.1176/ajp.154.1.50.
8
Iodine-123-iodobenzamide SPECT assessment of dopamine D2 receptor occupancy in riperidone-treated schizophrenic patients.碘-123-碘苯甲酰胺单光子发射计算机断层扫描评估利培酮治疗的精神分裂症患者多巴胺D2受体占有率
J Nucl Med. 1998 Jul;39(7):1138-42.
9
[123I]IBZM SPECT for imaging of striatal D2 dopamine receptors in 56 schizophrenic patients taking various neuroleptics.用[123I]碘苄酰胺单光子发射计算机断层扫描(SPECT)对56例服用各种抗精神病药物的精神分裂症患者的纹状体D2多巴胺受体进行成像。
Am J Psychiatry. 1996 Feb;153(2):183-90. doi: 10.1176/ajp.153.2.183.
10
Effect of haloperidol dose on iodine-123-IBZM brain SPECT imaging in schizophrenic patients.氟哌啶醇剂量对精神分裂症患者碘-123-IBZM脑单光子发射计算机断层扫描成像的影响。
J Nucl Med. 1997 Feb;38(2):203-7.

引用本文的文献

1
PET/CT imaging of the late-gestation fetal brain in pregnant rats: A proof-of-concept study.孕鼠妊娠晚期胎儿脑部的PET/CT成像:一项概念验证研究。
J Cereb Blood Flow Metab. 2025 Sep 8:271678X251370861. doi: 10.1177/0271678X251370861.
2
Neuroimaging glutamatergic mechanisms differentiating antipsychotic treatment-response.神经影像学谷氨酸能机制区分抗精神病药物治疗反应。
Sci Rep. 2023 Jun 2;13(1):8938. doi: 10.1038/s41598-022-26702-0.
3
Altered Patterns of Brain Glucose Metabolism Involve More Extensive and Discrete Cortical Areas in Treatment-resistant Schizophrenia Patients Compared to Responder Patients and Controls: Results From a Head-to-Head 2-[18F]-FDG-PET Study.
与应答者患者和对照相比,治疗抵抗性精神分裂症患者大脑葡萄糖代谢模式改变涉及更广泛和更离散的皮质区域:一项头对头 2-[18F]-FDG-PET 研究的结果。
Schizophr Bull. 2023 Mar 15;49(2):474-485. doi: 10.1093/schbul/sbac147.
4
Treatment-Resistant Schizophrenia: Genetic and Neuroimaging Correlates.难治性精神分裂症:遗传与神经影像学关联
Front Pharmacol. 2019 Apr 16;10:402. doi: 10.3389/fphar.2019.00402. eCollection 2019.
5
Treatment resistant schizophrenia: Clinical, biological, and therapeutic perspectives.治疗抵抗性精神分裂症:临床、生物学和治疗学视角。
Neurobiol Dis. 2019 Nov;131:104257. doi: 10.1016/j.nbd.2018.08.016. Epub 2018 Aug 29.
6
Distinguishing Between Treatment-Resistant and Non-Treatment-Resistant Schizophrenia Using Regional Homogeneity.利用局部一致性区分难治性与非难治性精神分裂症
Front Psychiatry. 2018 Aug 6;9:282. doi: 10.3389/fpsyt.2018.00282. eCollection 2018.
7
HAP1 Is Required for Endocytosis and Signalling of BDNF and Its Receptors in Neurons.HAP1 对于神经元中 BDNF 及其受体的内吞作用和信号转导是必需的。
Mol Neurobiol. 2018 Mar;55(3):1815-1830. doi: 10.1007/s12035-016-0379-0. Epub 2017 Jan 12.
8
Evidence for impaired glucose metabolism in the striatum, obtained postmortem, from some subjects with schizophrenia.在一些精神分裂症患者死后获得的纹状体葡萄糖代谢受损的证据。
Transl Psychiatry. 2016 Nov 15;6(11):e949. doi: 10.1038/tp.2016.226.
9
Brain-imaging studies of treatment-resistant schizophrenia: a systematic review.难治性精神分裂症的脑成像研究:一项系统综述
Lancet Psychiatry. 2016 May;3(5):451-63. doi: 10.1016/S2215-0366(15)00540-4. Epub 2016 Mar 4.
10
Treatment-Resistant Schizophrenia Patients Show Elevated Anterior Cingulate Cortex Glutamate Compared to Treatment-Responsive.与治疗有反应的精神分裂症患者相比,难治性精神分裂症患者前扣带回皮质谷氨酸水平升高。
Schizophr Bull. 2016 May;42(3):744-52. doi: 10.1093/schbul/sbv151. Epub 2015 Dec 17.