[1]邵继红,韩珍,杨艳,等. 白芍抗抑郁作用的实验研究[J]. 宁夏医学杂志,2008,30(6):490491.
[2]Kupfer D J, Frank E, Phillips M L. Major depressive disorder: new clinical, neurobiological, and treatment perspectives[J]. Lancet, 2012, 379(9820): 10451055.
[3]王景霞,张建军,李伟,等. 芍药苷抗抑郁作用与NO/cGMP通路相关性研究[J]. 中药与临床, 2012, 25(11): 2728.
[4]崔广智,金树梅. 芍药苷对利血平诱导抑郁模型的影响[J]. 中国实验方剂学杂志, 2012, 18(22): 272274.
[5]Belmaker R H, Agam G. Major depressive disorder[J]. N Engl J Med, 2008, 358(1): 5568.
[6]Mao Q Q, Ip S P, Ko K M, et al. Peony glycosides produce antidepressantlike action in mice exposed to chronic unpredictable mild stress: effects on hypothalamicpituitaryadrenal function and brainderived neurotrophic factor[J]. Prog Neuropsychopharmacol Biol Psychiatry, 2009, 33(7): 12111216.
[7]Mao Q Q, Xian Y F, Ip S P, et al. Protective effects of peony glycosides against corticosteroneinduced cell death in PC12 cells through antioxidant action[J]. J Ethnopharmacol, 2011, 133(3): 11211125.
[8]崔广智. 芍药苷抗抑郁作用的实验研究[J]. 现代药物与临床, 2009, 24(04): 231233.
[9]Duman R S, Monteggia L M. A neurotrophic model for stressrelated mood disorders[J]. Biol Psychiatry, 2006, 59(12): 11161127.
[10]Mao Q Q, Ip S P, Ko K M, et al. Effects of peony glycosides on mice exposed to chronic unpredictable stress: further evidence for antidepressantlike activity[J]. J Ethnopharmacol, 2009, 124(2): 316320.
[11]Golier J A, Schmeidler J, Legge J, et al. Twentyfour hour plasma cortisol and adrenocorticotropic hormone in Gulf War veterans: relationships to posttraumatic stress disorder and health symptoms[J]. Biol Psychiatry, 2007, 62(10): 11751178.
[12]Videbech P, Ravnkilde B, Pedersen A R, et al. The Danish PET/depression project: PET findings in patients with major depression[J]. Psychol Med, 2001, 31(7): 11471158.
[13]Nebes R D, Vora I J, Meltzer C C, et al. Relationship of deep white matter hyperintensities and apolipoprotein E genotype to depressive symptoms in older adults without clinical depression[J]. Am J Psychiatry, 2001, 158(6): 878884.
[14]Chen D M, Xiao L, Cai X, et al. Involvement of multitargets in paeoniflorininduced preconditioning[J]. J Pharmacol Exp Ther, 2006, 319(1): 165180.
[15]Liu J, Jin D Z, Xiao L, et al. Paeoniflorin attenuates chronic cerebral hypoperfusioninduced learning dysfunction and brain damage in rats[J]. Brain Res, 2006, 1089(1): 162170.
[16]杨煜,吕文伟,宋瑛士,等. 白芍总苷抗血栓形成作用[J]. 中草药, 2006, 37(7): 10661068.
[17]魏毅,张贵平. 黄芪多糖与白芍总苷对THP1巨噬细胞源性泡沫细胞内脂质的影响[J]. 中药新药与临床药理, 2007, 18(3): 189191.
[18]刘玮,吴华璞,祝晓光,等. 白芍总苷对全脑缺血再灌损伤的保护作用[J]. 中国药理学通报, 2004, 20(2): 211214.
[19]吴芳. 赤芍总苷/淫羊藿总黄酮对实验性抑郁及脑5HT和β肾上腺素受体的影响[J]. 现代预防医学, 2005, 32(7): 744746.
[20]何丽娜,杨军,何素冰,等. 赤芍总甙对原代培养大鼠神经细胞损伤模型的保护作用[J]. 中国临床药理学与治疗学, 2000, 5(1): 2831.
[21]马仁强,朱邦豪,陈健文,等. 赤芍总苷注射液对大鼠局灶性脑缺血的保护作用和脑血流量的影响[J]. 中成药, 2006, 28(6): 835838.
[22]李越兰,张世亮,张丽英,等. 柴胡白芍水煎剂对行为绝望抑郁模型小鼠的影响[J]. 甘肃中医学院学报, 2012, 29(3): 79.
[23]于春泉,李苒,张敏,等. 柴胡白芍药对抗抑郁作用的实验研究[J]. 中国实验方剂学杂志, 2012, 18(23): 286289.
[24]李越兰,张世亮,张丽英,等. 柴胡白芍水煎剂对慢性应激抑郁大鼠脑神经递质的影响[J]. 浙江中医杂志, 2012, 47(12): 912913.
[25]吴芳. 赤芍总苷/淫羊藿总黄酮对实验性抑郁及脑5HT和β肾上腺素受体的影响[J]. 现代预防医学, 2005, 32(7): 744746.
[26]陈文伟. 石菖蒲、赤芍醇提取物对实验性抑郁及血管活性肠肽和P物质的影响[J]. 华西医学, 2006, 21(2): 321322.