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酒精使用障碍的代谢型谷氨酸 5 受体多模态神经影像学及功能连接研究

Multimodal neuroimaging of metabotropic glutamate 5 receptors and functional connectivity in alcohol use disorder.

机构信息

Yale PET Center, Yale School of Medicine, New Haven, Connecticut, USA.

Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut, USA.

出版信息

Alcohol Clin Exp Res. 2022 May;46(5):770-782. doi: 10.1111/acer.14816. Epub 2022 Apr 21.

Abstract

BACKGROUND

People recovering from alcohol use disorder (AUD) show altered resting brain connectivity. The metabotropic glutamate 5 (mGlu5) receptor is an important regulator of synaptic plasticity potentially linked with synchronized brain activity and a target of interest in treating AUD. The goal of this work was to assess potential relationships of brain connectivity at rest with mGlu5 receptor availability in people with AUD at two time points early in abstinence.

METHODS

Forty-eight image data sets were acquired with a multimodal neuroimaging battery that included resting-state functional magnetic resonance imaging (fMRI) and mGlu5 receptor positron emission tomography (PET) with the radiotracer [ F]FPEB. Participants with AUD (n = 14) were scanned twice, at approximately 1 and 4 weeks after beginning supervised abstinence. [ F]FPEB PET results were published previously. Primary comparisons of fMRI outcomes were performed between the AUD group and healthy controls (HCs; n = 23) and assessed changes over time within the AUD group. Relationships between resting-state connectivity measures and mGlu5 receptor availability were explored within groups.

RESULTS

Compared to HCs, global functional connectivity of the orbitofrontal cortex was higher in the AUD group at 4 weeks of abstinence (p = 0.003), while network-level functional connectivity within the default mode network (DMN) was lower (p < 0.04). Exploratory multimodal analyses showed that mGlu5 receptor availability was correlated with global connectivity across all brain regions (HCs, r = 0.41; AUD group at 1 week of abstinence, r = 0.50 and at 4 weeks, r = 0.46; all p < 0.0001). Furthermore, a component of cortical and striatal mGlu5 availability was correlated with connectivity between the DMN and salience networks in HCs (r = 0.60, p = 0.003) but not in the AUD group (p > 0.3).

CONCLUSIONS

These preliminary findings of altered global and network connectivity during the first month of abstinence from drinking may reflect the loss of efficient network function, while exploratory relationships with mGlu5 receptor availability suggest a potential glutamatergic relationship with network coherence.

摘要

背景

从酒精使用障碍 (AUD) 中恢复的人表现出静息大脑连接的改变。代谢型谷氨酸 5 (mGlu5) 受体是突触可塑性的重要调节剂,可能与同步脑活动有关,也是治疗 AUD 的目标。这项工作的目的是评估 AUD 患者在开始戒酒后的头两个时间点,静息状态下的大脑连接与 mGlu5 受体可用性之间的潜在关系。

方法

使用包括静息态功能磁共振成像 (fMRI) 和放射性示踪剂 [F]FPEB 的代谢型谷氨酸 5 受体正电子发射断层扫描 (PET) 的多模态神经影像学组合,共采集了 48 个图像数据集。14 名 AUD 患者在开始监督性戒酒后的大约 1 周和 4 周时进行了两次扫描。[F]FPEB PET 结果之前已发表。在 AUD 组和健康对照组 (HCs; n=23) 之间进行了 fMRI 结果的主要比较,并评估了 AUD 组内的时间变化。在组内探索了静息状态连接测量值与 mGlu5 受体可用性之间的关系。

结果

与 HCs 相比,在戒酒后 4 周时,AUD 组的眶额皮质的全局功能连接更高(p=0.003),而默认模式网络 (DMN) 内的网络级功能连接更低(p<0.04)。探索性多模态分析显示,mGlu5 受体可用性与所有脑区的全局连接相关(HCs,r=0.41;AUD 组在戒酒后 1 周,r=0.50;在戒酒后 4 周,r=0.46;所有 p<0.0001)。此外,皮质和纹状体 mGlu5 可用性的一个成分与 HCs 中 DMN 和突显网络之间的连接相关(r=0.60,p=0.003),但在 AUD 组中不相关(p>0.3)。

结论

这些从饮酒中戒断的第一个月期间大脑全局和网络连接改变的初步发现可能反映了有效网络功能的丧失,而与 mGlu5 受体可用性的探索性关系表明与网络相干性的潜在谷氨酸能关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c46b/9117461/8fd85b867c7f/nihms-1793215-f0001.jpg

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