mGluR5 Facilitates Long-Term Synaptic Depression in a Stress-Induced Depressive Mouse Model

Xiangzhi Jiang, Wei Lin, Yuanyuan Cheng, Dongming Wang
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引用次数: 9

Abstract

Background Glutamatergic system has been known to play a role in the pathogenesis of major depression disorder by inducing N-methyl-d-aspartate receptor-dependent long-term depression (LTD) or metabotropic glutamate receptors (mGluR)-dependent LTD. Here, we characterized the LTD in a chronic social defeat stress (CSDS)-induced depressive mouse model. Methods CSDS was used to induce the depressive-like behaviors in C57BL/6 male mice, which were assessed using sucrose preference test and social interaction test. The synaptic strength including LTD and long-term potentiation (LTP) induced by paired-pulse low frequency stimulation (PP-LFS) was measured using whole-cell recording technique. Results CSDS induced depressive-like behaviors and facilitated PP-LFS-induced LTD in hippocampal CA3-CA1 pathway in the susceptible mice. Interestingly, mGluR5 but not N-methyl-d-aspartate receptor mediated the PP-LFS-induced LTD. In addition, mGluR5 agonist dihydroxyphenylglycine promoted PP-LFS-induced LTD specifically in susceptible mice, which was diminished by activating the BDNF/TrkB signaling pathway. Conclusions Our results suggest that mGluR5-dependent LTD might be responsible for the development of depressive-like behaviors in CSDS-induced depression mice model.
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mGluR5促进应激诱导抑郁小鼠模型的长期突触抑制
已知谷氨酸能系统通过诱导n -甲基-d-天冬氨酸受体依赖性长期抑郁(LTD)或代谢性谷氨酸受体(mGluR)依赖性长期抑郁(LTD)在重度抑郁症的发病机制中发挥作用。在这里,我们在慢性社会失败应激(CSDS)诱导的抑郁小鼠模型中表征了LTD。方法用CSDS诱导C57BL/6雄性小鼠抑郁样行为,采用蔗糖偏好测试和社会互动测试对其进行评价。采用全细胞记录技术测定配对脉冲低频刺激(PP-LFS)诱导的突触强度,包括LTP和LTP。结果CSDS诱导易感小鼠抑郁样行为,促进pp - lfs诱导的海马CA3-CA1通路的LTD。有趣的是,mGluR5而不是n -甲基-d-天冬氨酸受体介导pp - lfs诱导的LTD。此外,mGluR5激动剂二羟基苯基甘氨酸在易感小鼠中特异性地促进了pp - lfs诱导的LTD,通过激活BDNF/TrkB信号通路减少了LTD。结论mglur5依赖性LTD可能与csds诱导的抑郁小鼠模型中抑郁样行为的发生有关。
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