Publication | Open Access
Xiao Yao San Improves Depressive‐Like Behavior in Rats through Modulation of <i>β</i>‐Arrestin 2‐Mediated Pathways in Hippocampus
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Citations
39
References
2014
Year
Social IsolationXiao Yao SanPsychopharmacologySynaptic SignalingPsychologySocial SciencesMolecular PharmacologyDepressive‐like BehaviorNeuroendocrine MechanismHypothalamic PeptideDepression PathogenesisNeurochemistryStress BiomarkersNeurogeneticsMolecular NeuroscienceStress HormonePsychiatryBehavioral NeuroscienceXys ExtractsDepressionNeuropharmacologyPsychiatric DisorderEndocrinologyPharmacologyClinical DisordersSynaptic PlasticityNeuroscienceBiological PsychiatryMood DisordersMedicinePsychopathology
Xiao Yao San (XYS) is a classical Chinese medicine formula that has been widely used to treat mood disorders for hundreds of years. To confirm the effect of XYS and better understand its underlying mechanism, high-performance liquid chromatography-mass spectrometry analysis-based quality control of XYS extracts and proteomics-based identification of differential proteins in the hippocampus were adopted in social isolation and chronic unpredictable mild stress- (CUMS-) treated rats. The depressive-like behavior of rats induced by CUMS resembled the manifestation of human depression. The upregulated corticosterone (CORT) and urocortin 2 (UCN2) levels demonstrated the existence of hypothalamic-pituitary-adrenal (HPA) axis hyperactivity. XYS was effective in ameliorating the depressive-like behavior and downregulating UCN2 and CORT. XYS decreased the expression of serine/threonine-protein phosphatase 2A subunit B and increased the expression of β-arrestin 2. The expressions of brain-derived neurotrophic factor (BDNF), tyrosine receptor kinase B (TrkB), and mammalian target of rapamycin (mTOR) were also elevated by XYS. In conclusion, XYS improves social isolation and CUMS-induced depressive-like behavior and ameliorates HPA hyperactivation through the downregulation of corticotrophin releasing hormone (CRH) receptor 2. The upregulation of BDNF/TrkB and the phosphorylation of mTOR require β-arrestin 2 as a scaffold to regulate stress signaling.
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