[1] Gerald W Valentine, Gerard Sanacora. Targeting glial physiology and glutamate cycling in the treatment of depression [J]. Biochem Pharmacol, 2009, 78(5): 431-439.[2] Esra Kucukibrahimoglu, Melek Z Saygin, Mecit Caliskan, et al. The change in plasma GABA, glutamine and glutamate levels in fluoxetine- or S-citalopram-treated female patients with major depression [J]. Eur J Clin Pharmacol, 2009, 65(6): 571-577.[3] Barbara Begni, Lucio Tremolizzo, Cristina D'Orlando, et al. Substrate-induced modulation of glutamate uptake in human platelets [J]. Br J Pharmacol, 2005, 145(6): 792-799.[4] M J Lan, G A McLoughlin, J L Griffin, et al. Metabonomic analysis identifies molecular changes associated with the pathophysiology and drug treatment of bipolar disorder [J]. Mol Psychiatry, 2009, 14(3): 269-279.[5] Gregor Hasler, Jan Willem van der Veen, Toni Tumonis, et al. Reduced prefrontal glutamate/glutamine and gamma-aminobutyric acid levels in major depression determined using proton magnetic resonance spectroscopy [J]. Arch Gen Psychiatry, 2007, 64(2): 193-200.[6] Bettina Pfleiderer, Nikolaus Michael, Andreas Erfurth, et al. Effective electroconvulsive therapy reverses glutamate/glutamine deficit in the left anterior cingulum of unipolar depressed patients [J]. Psychiatry Res, 2003, 122 (3): 185-192.[7] Gerard Sanacora, Ralitza Gueorguieva, C Neill Epperson, et al. Subtype-specific alterations of gamma-aminobutyric acid and glutamate in patients with major depression [J]. Arch Gen Psychiatry, 2004, 61(7): 705-713.[8] Joanna M Wieronska, Beata Legutko, Dorota Dudys, et al. Olfactory bulbectomy and amitriptyline treatment influences mGlu receptors expression in the mouse brain hippocampus [J]. Pharmacol Rep, 2008, 60(6): 844-855.[9] M Zink, B Vollmayr, P J Gebicke-Haerter, et al. Reduced expression of glutamate transporters vGluT1, EAAT2 and EAAT4 in learned helpless rats, an animal model of depression [J]. Neuropharmacology, 2010, 58(2): 465-473.[10] J M Wieronska, P Branski, B Szewczyk, et al. Changes in the expression of metabotropic glutamate receptor 5 (mGluR5) in the rat hippocampus in an animal model of depression [J]. Pol J Pharmacol, 2001, 53(6): 659-662.[11] Ben Ryan, Laura Musazzi, Alessandra Mallei, et al. Remodelling by early-life stress of NMDA receptor-dependent synaptic plasticity in a gene-environment rat model of depression [J]. Int J Neuropsychopharmacol, 2009, 12(4): 553-559.[12] Ella Bossy-Wetzel, Robert Schwarzenbacher, Stuart A. Lipton. Molecular pathways to neurodegeneration [J]. Nat Med, 2004, 10 (Suppl): S2-S9.[13] Peter Vanhoutte, Himar Bading. Opposing roles of synaptic and extrasynaptic NMDA receptors in neuronal calcium signalling and BDNF gene regulation [J]. Curr Opin Neurobiol, 2003, 13 (3): 366-371.[14] P M Beart, R D O'Shea. Transporters for L-glutamate: an update on their molecular pharmacology and pathological involvement [J]. Br J Pharmacol, 2007, 150(1): 5-17.[15] P V Choudary, M Molnar, S J Evans, et al. Altered cortical glutamatergic and GABAergic signal transmission with glial involvement in depression [J]. Proc Natl Acad Sci USA, 2005, 102 (43): 15653-15658.[16] Leda S B Garcia, Clariss M Comim, Samira S Valvassori, et al. Ketamine treatment reverses behavioral and physiological alterations induced by chronic mild stress in rats [J]. Prog Neuropsychopharmacol Biol Psychiatry, 2009, 33(3): 450-455.[17] Li Nan-xin, Liu Rong-jian, Jason M Dwyer, et al. Glutamate N-methyl-D-aspartate receptor antagonists rapidly reverse behavioral and synaptic deficits caused by chronic stress exposure [J]. Biol Psychiatry, 2011, 69(8): 754-761.[18] 张欣, 汤颖, 王安宁, 等. 局部亚低温对大鼠脑缺血后凋亡细胞及谷氨酸转运体、亲代谢型谷氨酸受体表达的影响[J]. 临床神经病学杂志, 2007, 20: 360.[19] Jeffrey D Rothstein, Sarjubhai Patel, Melissa R Regan, et al. Beta-lactam antibiotics offer neuroprotection by increasing glutamate transporter expression [J]. Nature, 2005, 433(7021): 73-77.[20] Rita Sattler, Jeffrey D Rothstein. Targeting an old mechanism in a new disease-protection of glutamatergic dysfunction in depression [J]. Biol Psychiatry, 2007, 61(2): 137-138.[21] M Banasr, G M Chowdhury, R Terwilliger, et al. Glial pathology in an animal model of depression: reversal of stress-induced cellular, metabolic and behavioral deficits by the glutamate-modulating drug riluzole [J]. Mol Psychiatry, 2010, 15(5): 501-511.[22] M Smialowska, B Szewczyk, P Branski, et al. Effect of chronic imipramine or electroconvulsive shock on the expression of mGluR1a and mGluR5a immunoreactivity in rat brain hippocampus [J]. Neuropharmacology, 2002, 42(8): 1016-1023. |