The neural network of OCD, linking NHP and human studies
连接 NHP 和人类研究的强迫症神经网络
基本信息
- 批准号:9069072
- 负责人:
- 金额:$ 31.87万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:AbbreviationsAffectAmygdaloid structureAnimalsAnisotropyAnteriorAreaBasal GangliaBehaviorBiological Neural NetworksBrainCognitiveCorpus CallosumCorpus striatum structureDataDiffusion Magnetic Resonance ImagingDorsalEmotionalEmotionsFiberFunctional disorderGoalsHumanInternal CapsuleLinkLocationMonkeysMotorMotor CortexObsessive-Compulsive DisorderPathway interactionsPatientsPositioning AttributePrefrontal CortexRadialTestingTracerTravelVentral Striatumanatomical tracingbasecingulate cortexcingulotomycognitive controlcognitive systemfrontal lobehuman subjectinsightmotor controlneuroregulationnonhuman primateresearch studywhite matter
项目摘要
Project Summary
The pathophysiology of Obsessive Compulsive Disorder (OCD) is associated with dysfunction in prefrontal
cortical and basal-ganglia circuits, in particular the dorsal anterior cingulate cortex (dACC), orbital frontal cortex
(OFC), ventrolateral prefrontal cortex (vlPFC) and dorsal striatum. These areas are linked to regions involved
in both emotion (amygdala (amyg) and ventromedial PFC (vmPFC)) and higher cognitive and motor control
(dorsolateral PFC (dlPFC) and presupplementary motor cortex (pSMA)), placing them in a pivotal position for
bottom-up and top-down control for adapting behaviors appropriately. The dACC, vlPFC, and OFC fibers are
connected by the cingulum bundle (CB), corpus callosum (CC) and uncinate fasciculus (UF). These white
matter (WM) bundles, along with the internal capsule (IC) also show abnormalities in OCD. The overall goal of
P1 is to determine the connectivity between the dACC, vlPFC, OFC, and striatum, and the amyg/vmPFC, and
the dlPFC/ pSMA. We will use these data to explore connectivity abnormalities in OCD and the effects of
noninvasive stimulation and cingulotomy on the WM. Our first hypothesis is that within the dACC, OFC, vlPFC,
and striatum, there are specific regions (referred to as critical nodes) that contain converging terminal fields
from each other, and from the amyg and/or vmPFC, and from the dlPFC and/or pSMA. These critical nodes
would provide an anatomical substrate for modulation between emotional and cognitive systems. Our second
hypothesize is that the abnormalities in the WM found in OCD will be located within specific WM segments that
connect the critical nodes. Aim 1 will determine where critical nodes are located within the dACC, vlPFC, and
OFC and aim 2 will segment the CB, CC, UF, and IC based on where node connections travel. Aims 1 and 2
combine tracer experiments and diffusion MRI (dMRI) animals and dMRI in humans to locate the nodes and
segment the WM. Aim 3 will use the segmentation of WM is to evaluate more specifically connectivity
differences between OCD and healthy subjects and changes due to neuromodulation. The combination of
anatomical and dMRI experiments will provide a translational link for understanding the structural
underpinnings of connectivity changes associated with OCD.
项目摘要
强迫症(OCD)的病理生理学与前额叶功能障碍有关
皮质和基底囊式电路,尤其
(OFC),腹外侧前额叶皮层(VLPFC)和背纹状体。这些领域与涉及的地区有关
在情感(杏仁核(Amyg)和腹侧PFC(VMPFC))中,以及更高的认知和运动控制
(背外侧PFC(DLPFC)和预设运动皮层(PSMA)),将它们放在关键位置的位置
适当适当调整行为的自下而上和自上而下的控制。 DACC,VLPFC和OFC纤维是
由c束(CB),callosum callosum(CC)和Uncinate fasciculus(UF)连接。这些白色
物质(WM)束,以及内部胶囊(IC)也显示出强迫症的异常。总体目标
P1是确定DACC,VLPFC,OFC和Striatum和Amyg/vmpfc和
DLPFC/ PSMA。我们将使用这些数据来探索强迫症的连通性异常以及
WM上的非侵入性刺激和扣带切开术。我们的第一个假设是在DACC,OFC,VLPFC中,
和纹状体,有特定区域(称为关键节点)包含收敛的终端场
彼此,来自Amyg和/或VMPFC,以及DLPFC和/或PSMA。这些关键节点
将为情绪和认知系统之间的调节提供解剖基板。我们的第二个
假设是,OCD中发现的WM的异常将位于特定的WM段中
连接关键节点。 AIM 1将确定关键节点位于DACC,VLPFC和
OFC和AIM 2将根据节点连接的位置进行分割CB,CC,UF和IC。目标1和2
将示踪剂实验和扩散MRI(DMRI)动物和DMRI组合在人类中,以定位节点和
细分Wm。 AIM 3将使用WM的分割是为了评估更具体的连接性
强迫症和健康受试者之间的差异以及神经调节引起的变化。结合
解剖学和DMRI实验将为理解结构性提供转化链接
连通性变化的基础与强迫症相关。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Suzanne N Haber其他文献
Suzanne N Haber的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Suzanne N Haber', 18)}}的其他基金
BRAIN CONNECTS: The center for Large-scale Imaging of Neural Circuits (LINC)
大脑连接:神经回路大规模成像中心 (LINC)
- 批准号:
10672681 - 财政年份:2023
- 资助金额:
$ 31.87万 - 项目类别:
Persistent, Maladaptive Behaviors: Why We Make Bad Choices
持续的、适应不良的行为:为什么我们会做出错误的选择
- 批准号:
9261170 - 财政年份:2016
- 资助金额:
$ 31.87万 - 项目类别:
相似国自然基金
海洋缺氧对持久性有机污染物入海后降解行为的影响
- 批准号:42377396
- 批准年份:2023
- 资助金额:49 万元
- 项目类别:面上项目
氮磷的可获得性对拟柱孢藻水华毒性的影响和调控机制
- 批准号:32371616
- 批准年份:2023
- 资助金额:50 万元
- 项目类别:面上项目
还原条件下铜基催化剂表面供-受电子作用表征及其对CO2电催化反应的影响
- 批准号:22379027
- 批准年份:2023
- 资助金额:50 万元
- 项目类别:面上项目
CCT2分泌与内吞的机制及其对毒性蛋白聚集体传递的影响
- 批准号:32300624
- 批准年份:2023
- 资助金额:10 万元
- 项目类别:青年科学基金项目
在轨扰动影响下空间燃料电池系统的流动沸腾传质机理与抗扰控制研究
- 批准号:52377215
- 批准年份:2023
- 资助金额:50 万元
- 项目类别:面上项目
相似海外基金
Kappa Opioid Receptor in Paraventricular Nucleus of Thalamus
丘脑室旁核中的 Kappa 阿片受体
- 批准号:
10659960 - 财政年份:2023
- 资助金额:
$ 31.87万 - 项目类别:
Effects of binge ethanol on neuroinflammation and neurodegeneration with high fat diets
暴饮乙醇对高脂肪饮食引起的神经炎症和神经变性的影响
- 批准号:
10668068 - 财政年份:2023
- 资助金额:
$ 31.87万 - 项目类别:
Do allergens contribute to neurodegeneration?
过敏原会导致神经退行性变吗?
- 批准号:
10190052 - 财政年份:2021
- 资助金额:
$ 31.87万 - 项目类别:
Neural substrates of recent and remote cocaine memories
最近和遥远的可卡因记忆的神经基质
- 批准号:
8253308 - 财政年份:2012
- 资助金额:
$ 31.87万 - 项目类别:
Stressor controllability and anxiety: role of serotonin and prefrontal cortex.
压力源可控性和焦虑:血清素和前额叶皮层的作用。
- 批准号:
7918261 - 财政年份:2008
- 资助金额:
$ 31.87万 - 项目类别: