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Postpartum depression (PPD) causes maternal mortality, and has a high disability rate. In recent years, studies have suggested the Sirt1 gene to be involved in the pathogenesis of depression. Resveratrol (RSV), an activator of Sirt1, has been investigated in depressive behavior. However, its effect on PPD remains to be thoroughly elucidated.We employed a mice model with bilateral oophorectomy combined with hormone-simulated pregnancy to assess postpartum depression-like behavior. The behavioral tests were performed 2 days after the withdrawal of estradiol benzoate. RSV was administered subcutaneously to the PPD model mice. Several behavioral tests were executed, including the open field test, forced swimming test, and tail suspension test. Western blot analyses and immunofluorescence staining were used to evaluate protein expression levels of SIRT1, autophagy markers, and the AKT/mTOR.Postpartum depressive-like behavior was triggered following the withdrawal of estradiol benzoate after hormone-stimulated-pregnancy. RSV improved postpartum depressive-like behavior of mice via its upregulation of the SIRT1 and autophagy markers, such as Beclin1, ATG5 and LC3B. Also, the downregulation of the p62 protein expression was observed. More importantly, we also detected the inhibition of phosphorylated AKT and mTOR in the hippocampus of postpartum depressive-like mice.RSV could alleviate postpartum depression-like behavior in mice by stimulating the SIRT1, induce autophagy and inhibit the AKT/ mTOR signaling pathway.

Post-traumatic stress disorder is a major public health problem due to its frequency, chronicity, and disability that impact daily life. Studies have evidenced that the activation/inhibition of autophagy and excessive activation of microglia have a relationship with PTSD. For this purpose, C57BL/6 mice were employed to establish the post-traumatic stress disorder pathology mice model by conditioned fear and single prolonged stress (CF + SPS). Fluoxetine and PLX3397 were administered. PTSD-like behaviors were alleviated following fluoxetine treatment, evidenced via open field and conditioned fear test. Autophagy-associated proteins were upregulated, and inflammation factors were reduced after fluoxetine treatment. Microglia depletion mice showed a lower inflammatory level. In conclusion, fluoxetine can promote autophagy and inhibit neuroinflammation in mice model of PTSD, providing a theoretical basis for fluoxetine in treating PTSD.

Rag1 plays a critical role in the development and maturation of lymphocytes, and is related to immune memory functions. Deletion of Rag1 results in a lack of mature functional B and T lymphocytes. Rag1 transcription is most apparent in regions of the postnatal brain with high neuronal cell density - the cerebellum and the hippocampal formation, both of which are relevant to learning and memory function. In this research, three pairs of shRNA targeting Rag1 and a pair of scrambled sequences were constructed, packaged within a lentiviral vector system, and transferred into the cultured rat hippocampal neuron cells in vitro. Meanwhile, the lentivirus was injected stereotaxically into CA3 of the rat hippocampus, where the positive immunofluorescence for GFP expression was located. Rag1 mRNA expression was detected by RT-PCR 7, 14 and 28 days after stereotaxic injection. Assessment in the Morris water maze test 28 days post stereotaxic injection showed a loss of spatial learning and memory in the experimental rats. In long-term potentiation research, the experimental group did not display remarkable disparity in comparison with the control group. These findings indicate that the knockdown of Rag1 expression in the hippocampus may impair spatial learning and memory ability in rats.