Wu Bin, Guo Yuanyuan, Deng Jie, Chen Qibin, Min Su
Department of Anesthesiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Neuropsychiatr Dis Treat. 2021 May 11;17:1433-1442. doi: 10.2147/NDT.S304075. eCollection 2021.
Depression is a common mood disorder in humans worldwide. Electroconvulsive therapy (ECT) remains the most effective treatment for patients with drug-resistant or severe depression; however, during ECT, electrical resistance can occur, antagonizing ECT efficacy. We aimed to investigate how depressed patients develop resistance to electric shocks during ECT.
Rats exposed to chronic unpredictable stress exert similar impairments in hippocampal synaptic plasticity as those in depressed humans, including hippocampal neuronal atrophy and reduced synaptic function and synapse-related proteins. Therefore, a rat model was used to model depressive-like behaviors in the current study. Depression-like behavior was stimulated in Sprague Dawley (SD) rats that were then randomized into six groups: control group (C); a rat model of stress-induced depression group (D); and four groups in which a rat model of stress-induced depression received one, three, five, or seven electroconvulsive shocks (ECS; DE1, DE3, DE5, and DE7). The sucrose preference test (SPT) and Morris water maze (MWM) were utilized to evaluate anhedonia and spatial learning and memory in rats, respectively. Synaptic plasticity was recorded electrophysiologically in terms of field excitatory postsynaptic potential (fEPSP) and long-term potentiation (LTP).
The rat model of stress-induced depression triggered a decrease in the sucrose preference percentage (SPP) and the baseline fEPSP slope relative to those observed for the C group, and these changes were significantly rescued by ECT in a shock number-dependent manner within five shocks. However, the rat model of stress-induced depression displayed an increase in the escape latency and a decrease in space exploration time, in addition to decreased LTP relative to those in the C group, which was further augmented by ECT in a shock number-dependent manner within five shocks.
Changes in synaptic plasticity might be responsible for the development of resistance against constant-stimulus ECT in a rat model of stress-induced depression.
抑郁症是全球人类常见的情绪障碍。电休克疗法(ECT)仍然是治疗耐药性或重度抑郁症患者最有效的方法;然而,在ECT治疗期间,可能会出现电阻,对抗ECT的疗效。我们旨在研究抑郁症患者在ECT治疗期间如何产生电击抵抗。
暴露于慢性不可预测应激的大鼠在海马突触可塑性方面表现出与抑郁症患者类似的损伤,包括海马神经元萎缩、突触功能降低以及与突触相关的蛋白质减少。因此,在本研究中使用大鼠模型来模拟抑郁样行为。在斯普拉格-道利(SD)大鼠中诱导出抑郁样行为,然后将其随机分为六组:对照组(C);应激诱导抑郁症大鼠模型组(D);以及四组,其中应激诱导抑郁症大鼠模型分别接受1次、3次、5次或7次电休克(ECS;DE1、DE3、DE5和DE7)。分别利用蔗糖偏好试验(SPT)和莫里斯水迷宫(MWM)评估大鼠的快感缺失以及空间学习和记忆能力。根据场兴奋性突触后电位(fEPSP)和长时程增强(LTP),通过电生理记录突触可塑性。
应激诱导抑郁症大鼠模型相对于C组,蔗糖偏好百分比(SPP)和基线fEPSP斜率降低,并且在五次电击内,ECT以电击次数依赖的方式显著挽救了这些变化。然而,应激诱导抑郁症大鼠模型相对于C组,逃避潜伏期增加,空间探索时间减少,此外LTP降低,在五次电击内,ECT以电击次数依赖的方式进一步加剧了这些变化。
在应激诱导抑郁症大鼠模型中,突触可塑性的变化可能是对恒定刺激ECT产生抵抗的原因。