Kobayashi Katsunori, Imoto Yuki, Yamamoto Fumi, Kawasaki Mayu, Ueno Miyuki, Segi-Nishida Eri, Suzuki Hidenori
Department of Pharmacology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan;
Japan Science and Technology Agency, Core Research for Evolutional Science and Technology, Saitama, Japan.
J Neurophysiol. 2017 Jan 1;117(1):284-289. doi: 10.1152/jn.00740.2016. Epub 2016 Oct 26.
Electroconvulsive therapy (ECT) is an established effective treatment for medication-resistant depression with the rapid onset of action. However, its cellular mechanism of action has not been revealed. We have previously shown that chronic antidepressant drug treatments enhance dopamine D-like receptor-dependent synaptic potentiation at the hippocampal mossy fiber (MF)-CA3 excitatory synapse. In this study we show that ECT-like treatments in mice also have marked effects on the dopaminergic synaptic modulation. Repeated electroconvulsive stimulation (ECS), an animal model of ECT, strongly enhanced the dopamine-induced synaptic potentiation at the MF synapse in hippocampal slices. Significant enhancement was detectable after the second ECS, and further repetition of ECS up to 11 times monotonously increased the magnitude of enhancement. After repeated ECS, the dopamine-induced synaptic potentiation remained enhanced for more than 4 wk. These synaptic effects of ECS were accompanied by increased expression of the dopamine D receptor gene. Our results demonstrate that robust neuronal activation by ECS induces rapid and long-lasting enhancement of dopamine-induced synaptic potentiation at the MF synapse, likely via increased expression of the D receptor, at least in part. This rapid enhancement of dopamine-induced potentiation at the excitatory synapse may be relevant to the fast-acting antidepressant effect of ECT.
NEW & NOTEWORTHY: We show that electroconvulsive therapy (ECT)-like stimulation greatly enhances synaptic potentiation induced by dopamine at the excitatory synapse formed by the hippocampal mossy fiber in mice. The effect of ECT-like stimulation on the dopaminergic modulation was rapidly induced, maintained for more than 4 wk after repeated treatments, and most likely mediated by increased expression of the dopamine D1 receptor. These effects may be relevant to fast-acting strong antidepressant action of ECT.
电休克疗法(ECT)是一种公认的对药物抵抗性抑郁症有效的治疗方法,起效迅速。然而,其细胞作用机制尚未明确。我们之前已经表明,慢性抗抑郁药物治疗可增强海马苔藓纤维(MF)-CA3兴奋性突触处多巴胺D样受体依赖性的突触增强。在本研究中,我们发现小鼠中类似ECT的治疗对多巴胺能突触调制也有显著影响。重复电惊厥刺激(ECS),一种ECT的动物模型,强烈增强了海马切片中MF突触处多巴胺诱导的突触增强。在第二次ECS后可检测到显著增强,进一步重复ECS达11次可单调增加增强幅度。重复ECS后,多巴胺诱导的突触增强持续增强超过4周。ECS的这些突触效应伴随着多巴胺D受体基因表达的增加。我们的结果表明,ECS引起的强烈神经元激活至少部分地通过增加D受体的表达,诱导了MF突触处多巴胺诱导的突触增强的快速和持久增强。这种兴奋性突触处多巴胺诱导增强的快速增强可能与ECT的快速抗抑郁作用有关。
我们表明,类似电休克疗法(ECT)的刺激极大地增强了小鼠海马苔藓纤维形成的兴奋性突触处多巴胺诱导的突触增强。类似ECT的刺激对多巴胺能调制的作用在重复治疗后迅速诱导,持续超过4周,最有可能由多巴胺D1受体表达增加介导。这些效应可能与ECT快速强效的抗抑郁作用有关。