Carrette L L G, Santos A, Brennan M, Othman D, Collazo A, George O
Department of Psychiatry, UC San Diego, La Jolla, CA, United States.
Beckman Institute, CalTech, Passadena, CA, United States.
bioRxiv. 2024 Jan 14:2023.09.30.560339. doi: 10.1101/2023.09.30.560339.
Chronic alcohol consumption leads to dependence and withdrawal symptoms upon cessation, contributing to persistent use. However, the brain network mechanisms by which the brain orchestrates alcohol withdrawal and how these networks are affected by pharmacological treatments remain elusive. Recent work revealed that alcohol withdrawal produces a widespread increase in coordinated brain activity and a decrease in modularity of the whole-brain functional network using single-cell whole-brain imaging of immediate early genes. This decreased modularity and functional hyperconnectivity are hypothesized to be novel biomarkers of alcohol withdrawal in alcohol dependence, which could potentially be used to evaluate the efficacy of new medications for alcohol use disorder. However, there is no evidence that current FDA-approved medications or experimental treatments known to reduce alcohol drinking in animal models can normalize the changes in whole-brain functional connectivity. In this report, we tested the effect of R121919, a CRF1 antagonist, and naltrexone, an FDA-approved treatment for alcohol use disorder, on whole-brain functional connectivity using the cellular marker FOS combined with graph theory and advanced network analyses. Results show that both R121919 and naltrexone restored the functional connectivity of the prefrontal cortex during alcohol withdrawal, but through divergent mechanisms. Specifically, R121919 increased FOS activation in the prefrontal cortex, partially restored modularity, and normalized connectivity, particularly in CRF1-rich regions, including the prefrontal, pallidum, and extended amygdala circuits. On the other hand, naltrexone decreased FOS activation throughout the brain, decreased modularity, and increased connectivity overall except for the Mu opioid receptor-rich regions, including the thalamus. These results identify the brain networks underlying the pharmacological effects of R121919 and naltrexone and demonstrate that these drugs restored different aspects of functional connectivity of the prefrontal cortex, pallidum, amygdala, and thalamus during alcohol withdrawal. Notably, these effects were particularly prominent in CRF1- and Mu opioid receptors-rich regions highlighting the potential of whole-brain functional connectivity using FOS as a tool for identifying neuronal network mechanisms underlying the pharmacological effects of existing and new medications for alcohol use disorder.
长期饮酒会导致依赖,戒断时会出现戒断症状,从而促使持续饮酒。然而,大脑协调酒精戒断的脑网络机制以及这些网络如何受到药物治疗的影响仍然不清楚。最近的研究表明,使用即时早期基因的单细胞全脑成像技术发现,酒精戒断会导致全脑功能网络的协调性广泛增加,模块性降低。这种降低的模块性和功能超连接性被认为是酒精依赖中酒精戒断的新型生物标志物,有可能用于评估治疗酒精使用障碍新药的疗效。然而,没有证据表明目前美国食品药品监督管理局(FDA)批准的药物或已知能减少动物模型中酒精摄入的实验性治疗方法可以使全脑功能连接的变化恢复正常。在本报告中,我们使用细胞标记物FOS结合图论和先进的网络分析方法,测试了促肾上腺皮质激素释放因子1(CRF1)拮抗剂R121919和FDA批准的酒精使用障碍治疗药物纳曲酮对全脑功能连接的影响。结果表明,R121919和纳曲酮在酒精戒断期间均恢复了前额叶皮质的功能连接,但机制不同。具体而言,R121919增加了前额叶皮质中FOS的激活,部分恢复了模块性,并使连接性正常化,特别是在富含CRF1的区域,包括前额叶、苍白球和扩展杏仁核回路。另一方面,纳曲酮降低了全脑的FOS激活,降低了模块性,并总体上增加了连接性,但富含μ阿片受体的区域(包括丘脑)除外。这些结果确定了R121919和纳曲酮药理作用背后的脑网络,并表明这些药物在酒精戒断期间恢复了前额叶皮质、苍白球、杏仁核和丘脑功能连接的不同方面。值得注意的是,这些作用在富含CRF1和μ阿片受体的区域尤为突出,突出了使用FOS进行全脑功能连接作为一种工具来识别现有和新的酒精使用障碍治疗药物药理作用背后神经元网络机制的潜力。