Kuhn Marion, Mainberger Florian, Feige Bernd, Maier Jonathan G, Wirminghaus Mailies, Limbach Lotte, Mall Volker, Jung Nicolai H, Reis Janine, Klöppel Stefan, Normann Claus, Nissen Christoph
Department of Psychiatry and Psychotherapy, University Medical Center Freiburg, Freiburg, Germany.
Department of Pediatrics, Technische Universität München, Munich, Germany.
Neuropsychopharmacology. 2016 May;41(6):1521-9. doi: 10.1038/npp.2015.310. Epub 2015 Oct 7.
The synaptic plasticity hypothesis of major depressive disorder (MDD) posits that alterations in synaptic plasticity represent a final common pathway underlying the clinical symptoms of the disorder. This study tested the hypotheses that patients with MDD show an attenuation of cortical synaptic long-term potentiation (LTP)-like plasticity in comparison with healthy controls, and that this attenuation recovers after remission. Cortical synaptic LTP-like plasticity was measured using a transcranial magnetic stimulation protocol, ie, paired associative stimulation (PAS), in 27 in-patients with MDD according to ICD-10 criteria and 27 sex- and age-matched healthy controls. The amplitude of motor-evoked potentials was measured before and after PAS. Patients were assessed during the acute episode and at follow-up to determine the state- or trait-character of LTP-like changes. LTP-like plasticity, the PAS-induced increase in motor-evoked potential amplitudes, was significantly attenuated in patients with an acute episode of MDD compared with healthy controls. Patients with remission showed a restoration of synaptic plasticity, whereas the deficits persisted in patients without remission, indicative for a state-character of impaired LTP-like plasticity. The results provide first evidence for a state-dependent partial occlusion of cortical LTP-like plasticity in MDD. This further identifies impaired LTP-like plasticity as a potential pathomechanism and treatment target of the disorder.
重度抑郁症(MDD)的突触可塑性假说认为,突触可塑性的改变是该疾病临床症状背后的最终共同途径。本研究检验了以下假说:与健康对照相比,MDD患者的皮质突触长时程增强(LTP)样可塑性减弱,且这种减弱在缓解后恢复。根据ICD - 10标准,对27例住院的MDD患者和27例性别及年龄匹配的健康对照,使用经颅磁刺激方案,即配对联想刺激(PAS),来测量皮质突触LTP样可塑性。在PAS前后测量运动诱发电位的幅度。在急性期和随访期间对患者进行评估,以确定LTP样变化的状态或特质特征。与健康对照相比,MDD急性期患者的LTP样可塑性,即PAS诱导的运动诱发电位幅度增加,显著减弱。缓解的患者显示突触可塑性恢复,而未缓解的患者缺陷持续存在,表明LTP样可塑性受损具有状态特征。这些结果为MDD中皮质LTP样可塑性的状态依赖性部分阻断提供了首个证据。这进一步确定了受损的LTP样可塑性是该疾病的潜在发病机制和治疗靶点。