%0 Journal Article
%T Role of mitochondria-associated membranes in the hippocampus in the pathogenesis of depression.
%A Zhang JR
%A Shen SY
%A Shen ZQ
%A Yin SY
%A Ye K
%A Li W
%A Li HY
%A Liang LF
%A Wang YQ
%A Guo XY
%A Yu J
%J J Affect Disord
%V 361
%N 0
%D 2024 Jun 22
%M 38914161
%F 6.533
%R 10.1016/j.jad.2024.06.076
%X <B>BACKGROUND: </B>Pathological changes, such as microglia activation in the hippocampus frequently occur in individuals with animal models of depression; however, they may share a common cellular mechanism, such as endoplasmic reticulum (ER) stress and mitochondrial dysfunction. Mitochondria associated membranes (MAMs) are communication platforms between ER and mitochondria. This study aimed to investigate the role of intracellular stress responses, especially structural and functional changes of MAMs in depression.<BR><B>METHODS: </B>We used chronic social defeat stress (CSDS) to mimic depression in C57 mice to investigate the pathophysiological changes in the hippocampus associated with depression and assess the antidepressant effect of electroacupuncture (EA). Molecular, histological, and electron microscopic techniques were utilized to study intracellular stress responses, including the ER stress pathway reaction, mitochondrial damage, and structural and functional changes in MAMs in the hippocampus after CSDS. Proteomics technology was employed to explore protein-level changes in MAMs caused by CSDS.<BR><B>RESULTS: </B>CSDS caused mitochondrial dysfunction, ER stress, closer contact between ER and mitochondria, and enrichment of functional protein clusters at MAMs in hippocampus along with depressive-like behaviors. Also, EA showed beneficial effects on intracellular stress responses and depressive-like behaviors in CSDS mice.<BR><B>CONCLUSIONS: </B>The cellular specificity of MAMs related protein changes in CSDS mice was not explored.<BR><B>CONCLUSIONS: </B>In the hippocampus, ER stress and mitochondrial damage occur, along with enriched mitochondria-ER interactions and MAM-related protein enrichment, which may contribute to depression's pathophysiology. EA may improve depression by regulating intracellular stress responses.