Research progress in animal models and mechanism of depression
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    Abstract:

    The incidence of depressive illness is high worldwide, and the inadequacy of currently available drug treatments contributes to the significant health burden associated with depression. Animal models of depression used as the main methods to study the pathogenesis mechanism and select effective drugs receive increasing concerns. Current popular models of depression creatively merge ethologically valid behavioral assays with the latest technological advances in molecular biology. In this context, this study aims to review the animal models of depression and pathogenesis related with face validity, construct validity, and predictive validity of these models. These models include stress-induced models, injury-induced models, drug-induced models and transgenic models which all mimic the depression symptoms of human to some degree and are of great value for developing new antidepressant drugs and studying the pathogenesis of this disease.

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    [1] Whiteford HA, Degenhardt L, Rehm J,et al. Global burden of disease attributable to mental and substance use disorders:findings from the Global Burden of Disease Study 2010[J]. Lancet,2013, 382(9904):1575-1586.
    [2] 邓佳慧,李素霞,董问天,等. 难治性抑郁症治疗的研究进展[J]. 中国神经精神疾病杂志, 2014,40(3):189-192.
    [3] Abelaira HM, Reus GZ, Quevedo J. Animal models as tools to study the pathophysiology of depression[J]. Revista Brasil Psiquiatria, 2013, 35(Suppl 2):112-120.
    [4] Stepanichev M, Dygalo NN, Grigoryan G,et al. Rodent models of depression:neurotrophic and neuroinflammatory biomarkers[J]. BioMed Res Int, 2014,932757.
    [5] Nabeshima T, Kim HC. Involvement of genetic and environmental factors in the onset of depression[J]. Exp Neurobiol, 2013, 22(4):235-243.
    [6] Wiborg O. Chronic mild stress for modeling anhedonia[J]. Cell Tissue Res, 2013,354(1):155-169.
    [7] Sun JD, Liu Y, Yuan YH,et al. Gap junction dysfunction in the prefrontal cortex induces depressive-like behaviors in rats[J]. Neuropsychopharmacology, 2012, 37(5):1305-1320.
    [8] Cao X, Li LP, Wang Q,et al. Astrocyte-derived ATP modulates depressive-like behaviors[J]. Nature Med, 2013,19(6):773-777.
    [9] Henningsen K, Palmfeldt J, Christiansen S, et al. Candidate hippocampal biomarkers of susceptibility and resilience to stress in a rat model of depression[J]. Mol Cellul Proteomics,2012, 11(70):1-35.
    [10] Bergstrom A, Jayatissa MN, Thykjaer T,et al. Molecular pathways associated with stress resilience and drug resistance in the chronic mild stress rat model of depression:a gene expression study[J]. J Mol Neurosci,2007,33(2):201-215.
    [11] Farhang S, Barar J, Fakhari A,et al. Asymmetrical expression of BDNF and NTRK3 genes in frontoparietal cortex of stress-resilient rats in an animal model of depression[J]. Synapse, 2014,68(9):387-393.
    [12] Fortune ES, Rose GJ. Short-term synaptic plasticity as a temporal filter[J]. Trends Neurosci, 2001,24(7):381-385.
    [13] Vollmayr B, Gass P. Learned helplessness:unique features and translational value of a cognitive depression model[J]. Cell Tissue Res, 2013, 354(1):171-178.
    [14] Li K, Zhou T, Liao L,et al. betaCaMKⅡ in lateral habenula mediates core symptoms of depression[J]. Science, 2013,341(6149):1016-1020.
    [15] Ridder S, Chourbaji S, Hellweg R,et al. Mice with genetically altered glucocorticoid receptor expression show altered sensitivity for stress-induced depressive reactions[J]. J Neurosci,2005,25(26):6243-6250.
    [16] Nishi M, Horii-Hayashi N, Sasagawa T. Effects of early life adverse experiences on the brain:implications from maternal separation models in rodents[J]. Fronti Neurosci, 2014,17(8):ecollection2014.00166.
    [17] Ellenbroek BA, Cools AR. The long-term effects of maternal deprivation depend on the genetic background[J]. Neuropsychopharmacology,2000,23(1):99-106.
    [18] 薛晓芳,李曼,王玮文,等. 母婴分离的动物模型及其神经生物学机制[J]. 心理科学进展,2013, 21(6):990-998.
    [19] O'Connor RM, Grenham S, Dinan TG,et al. microRNAs as novel antidepressant targets:converging effects of ketamine and electroconvulsive shock therapy in the rat hippocampus[J]. Int J Neuropsychopharmacol,2013, 16(8):1885-1892.
    [20] Patel PD, Lopez JF, Lyons DM,et al. Glucocorticoid and mineralocorticoid receptor mRNA expression in squirrel monkey brain[J]. J Psychiatr Res, 2000,34(6):383-392.
    [21] Rawashdeh O, Dubocovich ML. Long-term effects of maternal separation on the responsiveness of the circadian system to melatonin in the diurnal nonhuman primate (Macaca mulatta)[J]. J Pineal Res, 2014,56(3):254-263.
    [22] 祁可可,冯敏,孟肖路,等. 树鼩的社会挫败抑郁模型[J].心理科学进展2012,20(11):1787-1793.
    [23] Willard SL, Riddle DR, Forbes ME,et al. Cell number and neuropil alterations in subregions of the anterior hippocampus in a female monkey model of depression[J]. Biol Psychiatr, 2013,74(12):890-897.
    [24] Song C, Leonard BE. The olfactory bulbectomised rat as a model of depression[J]. Neurosci Biobehav Rev, 2005,29(4-5):627-647.
    [25] Morales-Medina JC, Juarez I, Venancio-Garcia E,et al. Impaired structural hippocampal plasticity is associated with emotional and memory deficits in the olfactory bulbectomized rat[J]. Neuroscience, 2013,236(16):233-243.
    [26] El-Bakly WM, Hasanin AH. Hypericum perforatum decreased hippocampus TNF-alpha and corticosterone levels with no effect on kynurenine/tryptophan ratio in bilateral ovariectomized rats[J]. Korean J Physiol pharmacol,2014,18(3):233-239.
    [27] Sukoff Rizzo SJ, Neal SJ, Hughes ZA,et al. Evidence for sustained elevation of IL-6 in the CNS as a key contributor of depressive-like phenotypes[J]. Translat Psychiatr, 2012,2:e199.
    [28] Kubera M, Curzytek K, Duda W,et al. A new animal model of (chronic) depression induced by repeated and intermittent lipopolysaccharide administration for 4 months[J]. Brain Behav Immunity, 2013,31:96-104.
    [29] Felger JC, Mun J, Kimmel HL,et al. Chronic interferon-alpha decreases dopamine 2 receptor binding and striatal dopamine release in association with anhedonia-like behavior in nonhuman primates[J].Neuropsychopharmacology,2013,38(11):2179-2187.
    [30] Lee MJ, Wei JW. The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortex[J]. Chin J Physiol, 2013,56(4):199-208.
    [31] Bao S, Fei J, Shen J,et al. Reserpine-induced model of stress suppresses mucosal immunity[J]. Immunol Cell Biol, 2006,84(6):537-542.
    [32] Arora V, Chopra K. Possible involvement of oxido-nitrosative stress induced neuro-inflammatory cascade and monoaminergic pathway:underpinning the correlation between nociceptive and depressive behaviour in a rodent model[J]. J Affect Disorders[J]. 2013,151(3):1041-1052.
    [33] Renoir T, Pang TY, Lanfumey L. Drug withdrawal-induced depression:serotonergic and plasticity changes in animal models[J]. Neurosci Biobehav Rev, 2012,36(1):696-726.
    [34] Fernandez SP, Gaspar P. Investigating anxiety and depressive-like phenotypes in genetic mouse models of serotonin depletion[J]. Neuropharmacology, 2012,62(1):144-154.
    [35] Gass P, Reichardt HM, Strekalova T,et al. Mice with targeted mutations of glucocorticoid and mineralocorticoid receptors:models for depression and anxiety?[J].Physiol Behav, 2001,73(5):811-825.
    [36] Willner P, Belzung C.Treatment-resistant depression:are animal models of depression fit for purpose?[J]. Psychopharmacology,2015, 232(19):3473-3495.
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  • Received:December 28,2015
  • Online: July 01,2016
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