A prophylactic effect of macrophage-colony stimulating factor on chronic stress-induced depression-like behaviors in mice

被引:11
|
作者
Ji, Jianlin [1 ]
Xiang, Haitao [2 ]
Lu, Xu [1 ]
Tan, Pingping [1 ]
Yang, Rongrong [3 ]
Ye, Ting [1 ]
Chen, Zhuo [4 ]
Chen, Dongjian [4 ]
He, Haiyan [5 ]
Chen, Jinliang [5 ]
Ma, Yaoying [1 ]
Huang, Chao [1 ]
机构
[1] Nantong Univ, Sch Pharm, Dept Pharmacol, 19 Qixiu Rd, Nantong 226001, Jiangsu, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Suzhou Kowloon Hosp, Dept Neurosurg, 118 Wansheng St, Suzhou 215028, Jiangsu, Peoples R China
[3] Nantong Univ, Affiliated Hosp, Dept Anesthesiol, 20 Xisi Rd, Nantong 226001, Jiangsu, Peoples R China
[4] Nantong Univ, Affiliated Hosp 2, Nantong Peoples Hosp 1, Invas Technol Dept, 6 North Rd Haier Xiang, Nantong 226001, Jiangsu, Peoples R China
[5] Nantong Univ, Affiliated Hosp 2, Nantong Peoples Hosp 1, Dept Resp Med, 6 North Rd Haier Xiang, Nantong 226001, Jiangsu, Peoples R China
关键词
Innate immune activation; Macrophage-colony stimulating factor; Prevention; Neuroinflammation; ALZHEIMERS-DISEASE; FACTOR-RECEPTOR; MICROGLIA; BRAIN; ACTIVATION; NEUROINFLAMMATION; ANTIDEPRESSANTS; INHIBITION; EXPRESSION; NEURONS;
D O I
10.1016/j.neuropharm.2021.108621
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Innate immune activation has been shown to reduce the severity of nervous system disorders such as brain ischemia and traumatic brain damage. Macrophage-colony stimulating factor (M-CSF), a drug that is used to treat hematological system disease, is an enhancer of the innate immune response. In the present study, we evaluated the effect of M-CSF preconditioning on chronic social defeat stress (CSDS)-induced depression-like behaviors in mice. Results showed that a single M-CSF injection 1 day before stress exposure at the dose of 100 and 500 mu g/kg, or a single M-CSF injection (100 mu g/kg) 1 or 5 days but not 10 days before stress exposure prevented CSDSinduced depression-like behaviors in mice. Further analysis showed that a second M-CSF injection 10 days after the first M-CSF injection and a 2 x or 4 x M-CSF injections 10 days before stress exposure also prevented CSDS-induced depression-like behaviors. Molecular studies revealed that a single M-CSF injection prior to stress exposure skewed the neuroinflammatory responses in the brain in CSDS-exposed mice towards an antiinflammatory phenotype. These behavioral and molecular actions of M-CSF were correlated with innate immune stimulation, as pre-inhibiting the innate immune activation by minocycline pretreatment (40 mg/kg) abrogated the preventive effect of M-CSF on CSDS-induced depression-like behaviors and neuroinflammatory responses. These results provide evidence to show that innate immune activation by M-CSF pretreatment may prevent chronic stress-induced depression-like behaviors via preventing the development of neuroinflammatory response in the brain, which may help to develop novel strategies for the prevention of depression.
引用
收藏
页数:13
相关论文
共 50 条
  • [21] Negative air ion exposure ameliorates depression-like behaviors induced by chronic mild stress in mice
    Yun-Qing Hu
    Ting-Ting Niu
    Jian-ming Xu
    Li Peng
    Qing-Hua Sun
    Ying Huang
    Ji Zhou
    Yu-Qiang Ding
    Environmental Science and Pollution Research, 2022, 29 : 62626 - 62636
  • [22] Negative air ion exposure ameliorates depression-like behaviors induced by chronic mild stress in mice
    Hu, Yun-Qing
    Niu, Ting-Ting
    Xu, Jian-Ming
    Peng, Li
    Sun, Qing-Hua
    Huang, Ying
    Zhou, Ji
    Ding, Yu-Qiang
    ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2022, 29 (41) : 62626 - 62636
  • [23] A novel probiotic formula, BLLL, ameliorates chronic stress-induced depression-like behaviors in mice by reducing neuroinflammation and increasing neurotrophic factors
    Ye, Minxiu
    Ji, Feng
    Huang, Chao
    Li, Fu
    Zhang, Changliang
    Zhang, Yu
    Wang, Runxin
    Ma, Kai
    Lu, Xu
    Wang, Hui
    FRONTIERS IN PHARMACOLOGY, 2024, 15
  • [24] p75NTR mediated chronic restraint stress-induced depression-like behaviors in mice via hippocampal mTOR pathway
    Peng, Yu-Yuan
    Tang, Can
    Wang, Hai-Yan
    Ding, Yang
    Yang, Huan
    Ma, Xin-Mei
    Gao, Jie
    Li, Sen
    Long, Zai-Yun
    Lu, Xiu-Min
    Wang, Yong-Tang
    LIFE SCIENCES, 2024, 358
  • [25] Intranasal administration of lipopolysaccharide reverses chronic stress-induced depression-like behavior in mice by microglial stimulation
    Huang, Chao
    Ye, Ting
    Chen, Bingran
    Chen, Zhuo
    Ye, Ying
    Liu, Huijun
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2023, 120
  • [26] Treatment of sulphasalazine-induced agranulocytosis with granulocyte macrophage-colony stimulating factor
    Roddie, P
    Dorrance, H
    Cook, MK
    Rainey, JB
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 1995, 9 (06) : 711 - 712
  • [27] Androgens suppress osteoclast formation induced by RANKL and macrophage-colony stimulating factor
    Huber, DM
    Bendixen, AC
    Pathrose, P
    Srivastava, S
    Dienger, KM
    Shevde, NK
    Pike, JW
    ENDOCRINOLOGY, 2001, 142 (09) : 3800 - 3808
  • [28] Effects of fluoxetine, tianeptine and olanzapine on unpredictable chronic mild stress-induced depression-like behavior in mice
    Mutlu, Oguz
    Gumuslu, Esen
    Ulak, Guner
    Celikyurt, Ipek Komsuoglu
    Kokturk, Sibel
    Kir, Hale Maral
    Akar, Furuzan
    Erden, Faruk
    LIFE SCIENCES, 2012, 91 (25-26) : 1252 - 1262
  • [29] Oral microbiota dysbiosis alters chronic restraint stress-induced depression-like behaviors by modulating host metabolism
    Lou, Fangzhi
    Luo, Shihong
    Kang, Ning
    Yan, Li
    Long, Huiqing
    Yang, Lu
    Wang, Haiyang
    Liu, Yiyun
    Pu, Juncai
    Xie, Peng
    Ji, Ping
    Jin, Xin
    PHARMACOLOGICAL RESEARCH, 2024, 204
  • [30] Prophylactic Effects of n-Acethylcysteine on Inflammation-induced Depression-like Behaviors in Mice
    Wang, Zhenhuan
    Hu, Qi
    Tian, Chao
    Wang, Ruipeng
    Jiao, Qingyan
    Chen, Feng
    Wu, Tongrui
    Wang, Jialiang
    Zhu, Yuxuan
    Liu, Aili
    Zhang, Wei
    Li, Jie
    Shen, Hui
    NEUROSCIENCE, 2024, 549 : 42 - 54