Effects of Jiaotaiwan on depressive-like behavior in mice after lipopolysaccharide administration

被引:43
作者
Qian Zhe [1 ]
Wang Sulei [1 ]
Tao Weiwei [2 ]
Long Hongyan [3 ]
Wang Jianwei [1 ]
机构
[1] Nanjing Univ Chinese Med, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Sch Basic Biomed Sci, Ctr Translat Syst Biol & Neurosci, Nanjing 210023, Jiangsu, Peoples R China
[3] Third Affiliated Hosp Nanjing Univ Chinese Med, Nanjing Municipal Hosp Chinese Med, Cent Lab, Nanjing 210001, Jiangsu, Peoples R China
关键词
Jiaotaiwan; Depression-like behavior; NF-kappa B signaling; TUMOR-NECROSIS-FACTOR; MEDIAL PREFRONTAL CORTEX; TAIL SUSPENSION TEST; POSTPARTUM DEPRESSION; RECEPTOR BLOCKADE; MILD STRESS; MOUSE MODEL; ANTIDEPRESSANTS; EXPRESSION; CYTOKINES;
D O I
10.1007/s11011-016-9925-8
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Jiao-Tai-Wan (JTW), has been usually used for insomnia in traditional Chinese medicine (TCM). The previous study shown that JTW was benefit for depression-like behavior, but the possible mechanism is not clear. This study is to determine whether JTW was benefit for the treatment of lipopolysaccharide (LPS)-induced depression-like behavior in mice and explore its possible mechanism. All drugs were intragastrically administered once daily for 7 consecutive days. On the 7th day, LPS was injected into mice 30 min after drug administration. Behavioral tests were performed 24 h after LPS administration. Serum levels of interleukin (IL)-6 and tumor necrosis factor (TNF)-alpha were measured by enzyme-linked immunosorbent assay (ELISA). The 5-hydroxytryptamine (5-HT) and nor-epinephrine (NE) levels in prefrontal cortex were determined by UPLC-MS. The protein expressions of NF-kappa B signaling in prefrontal cortex were determined by western blot. Behavioral tests were measured via tail suspension test (TST), forced swimming test (FST), sucrose preference test (SPT) and open field test (OFT). In addition, effects of JTW on the TNF-alpha induced depressive-like behavior were also examined. Pretreatment with JTW (4.2 and 8.4 g/kg) or fluoxetine (20 mg/kg) effectively attenuated LPS-induced upregulations of the serum TNF-alpha and IL-6 contents and JTW (4.2 and 8.4 g/kg) or fluoxetine (20 mg/kg) effectively increased the contents of 5-HT and NE compared with LPS-treated group. Meanwhile, the western blot analysis results indicated the correlation between the antidepressant activity of JTW and the regulation of NF-kappa B signaling in brain. Besides, JTW (4.2 and 8.4 g/kg) or fluoxetine (20 mg/kg) significantly shortened LPS-induced increases in immobility time of TST, FST and weakened the reduction of the sucrose preference in SPT without significant alterations of locomotor activity in OFT. Additionally, JTW effectively reversed the depressive-like behavior induced by TNF-alpha (0.1 fg/site, i.c.v.). Our findings indicated that Jiao-Tai-Wan (JTW) played an important role in monoaminergic response and anti-inflammation in lipopolysaccharide (LPS)-induced mouse model, which may be therapeutically exploited to alleviate depression-like behavior.
引用
收藏
页码:415 / 426
页数:12
相关论文
共 48 条
[1]
Medial prefrontal cortex lesions in the female rat affect sexual and maternal behavior and their sequential organization [J].
Afonso, Veronica M. ;
Sison, Margarette ;
Lovic, Vedran ;
Fleming, Alison S. .
BEHAVIORAL NEUROSCIENCE, 2007, 121 (03) :515-526
[2]
Signal transduction by tumor necrosis factor and its relatives [J].
Baud, V ;
Karin, M .
TRENDS IN CELL BIOLOGY, 2001, 11 (09) :372-377
[3]
Changes in behaviour and cytokine expression upon a peripheral immune challenge [J].
Bay-Richter, Cecilie ;
Janelidze, Shorena ;
Hallberg, Ludvig ;
Brundin, Lena .
BEHAVIOURAL BRAIN RESEARCH, 2011, 222 (01) :193-199
[4]
Immune system to brain signaling: Neuropsychopharmacological implications [J].
Capuron, Lucile ;
Miller, Andrew H. .
PHARMACOLOGY & THERAPEUTICS, 2011, 130 (02) :226-238
[5]
Chen T., 2015, FREE RADICAL RES, P1
[6]
Anti-Asthmatic Effects of Ginsenoside Rb1 in a Mouse Model of Allergic Asthma Through Relegating Th1/Th2 [J].
Chen, Tong ;
Xiao, Lu ;
Zhu, Lingpeng ;
Ma, Shiping ;
Yan, Tianhua ;
Ji, Hui .
INFLAMMATION, 2015, 38 (05) :1814-1822
[7]
Protective effect of platycodin D on liver injury in alloxan-induced diabetic mice via regulation of Treg/Th-17 balance [J].
Chen, Tong ;
Gao, Jin ;
Xiang, Pengjun ;
Chen, Yongde ;
Ji, Jing ;
Xie, Peng ;
Wu, Hui ;
Xia, Wei ;
Wei, Yidan ;
Wang, Shumin ;
Lan, Li ;
Ji, Hui ;
Yan, Tianhua .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2015, 26 (02) :338-348
[8]
The protective effect of CDDO-Me on lipopolysaccharide-induced acute lung injury in mice [J].
Chen, Tong ;
Mou, Yi ;
Tan, Jiani ;
Wei, Linlin ;
Qiao, Yixue ;
Wei, Tingting ;
Xiang, Pengjun ;
Peng, Sixun ;
Zhang, Yihua ;
Huang, Zhangjian ;
Ji, Hui .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2015, 25 (01) :55-64
[9]
Chojnacki C, 2015, J PHYSIOL PHARMACOL, V66, P665
[10]
Time course of the effects of lipopolysaccharide on prepulse inhibition and brain nitrite content in mice [J].
Custodio, Charllyany Sabino ;
Ferreira Mello, Bruna Stefania ;
Cordeiro, Rafaela Carneiro ;
Ramos de Araujo, Fernanda Yvelize ;
Chaves, Joao Henrique ;
Mendes Vasconcelos, Silvania Maria ;
Nobre Junior, Helio Vitoriano ;
Florenco de Sousa, Francisca Clea ;
Vale, Mariana Lima ;
Carvalho, Andre Ferrer ;
Macedo, Danielle Silveira .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2013, 713 (1-3) :31-38