Partial resistance to citalopram in a Wistar–Kyoto rat model of depression: An evaluation using resting-state functional MRI and graph analysis

西酞普兰 纹状体 生理盐水 内分泌学 内科学 心理学 再摄取抑制剂 难治性抑郁症 血清素 行为绝望测验 抗抑郁药 再摄取 神经科学 化学 药理学 医学 多巴胺 海马体 受体
作者
Qi Li,Wentao Zhao,Sha Li,Yu Zhao,Wei‐Xing Pan,Xiao Wang,Zhifen Liu,Yong Xu
出处
期刊:Journal of Psychiatric Research [Elsevier]
卷期号:151: 242-251 被引量:6
标识
DOI:10.1016/j.jpsychires.2022.04.010
摘要

Wistar–Kyoto (WKY) rats as an endogenous depression model partially lack a response to classic selective serotonin reuptake inhibitors (SSRIs). Thus, this strain has the potential to be established as a model of treatment-resistant depression (TRD). However, the SSRI resistance in WKY rats is still not fully understood. In this study, WKY and control rats were subjected to a series of tests, namely, a forced swim test (FST), a sucrose preference test (SPT), and an open field test (OFT), and were scanned in a 7.0-T MRI scanner before and after three-week citalopram or saline administration. Behavioral results demonstrated that WKY rats had increased immobility in the FST and decreased sucrose preference in the SPT and central time spent in the OFT. However, citalopram did not improve immobility in the FST. The amplitude of low-frequency fluctuation (ALFF) analysis showed regional changes in the striatum and hippocampus of WKY rats. However, citalopram partially reversed the ALFF value in the dorsal part of the two regions. Functional connectivity (FC) analysis showed that FC strengths were decreased in WKY rats compared with controls. Nevertheless, citalopram partially increased FC strengths in WKY rats. Based on FC, global graph analysis demonstrated decreased network efficiency in WKY + saline group compared with control + saline group, but citalopram showed weak network efficiency improvement. In conclusion, resting-state fMRI results implied widely affected brain function at both regional and global levels in WKY rats. Citalopram had only partial effects on these functional changes, indicating a potential treatment resistance mechanism.
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