Serotonin regulates brain-derived neurotrophic factor expression in select brain regions during acute psychological stress

被引:37
作者
Jiang, De-guo [1 ]
Jin, Shi-li [2 ]
Li, Gong-ying [2 ,3 ]
Li, Qing-qing [3 ]
Li, Zhi-ruo [2 ]
Ma, Hong-xia [3 ]
Zhuo, Chuan-jun [1 ,3 ,4 ]
Jiang, Rong-huan [5 ]
Ye, Min-jie [6 ]
机构
[1] Wenzhou 7th Peoples Hosp, Dept Psychiat, Wenzhou, Zhejiang, Peoples R China
[2] Jining Med Univ, Affiliated Hosp 2, Dept Psychiat, Jining, Shandong, Peoples R China
[3] Jining Med Univ, Dept Psychiat, Jining, Shandong, Peoples R China
[4] Tianjin Anding Hosp, Dept Psychiat, Tianjin, Peoples R China
[5] Chinese PLA Med Sch, Dept Psychol Med, Chinese PLA Gen Hosp, Dept Psychol Med, Beijing, Peoples R China
[6] Wenzhou Med Univ, Affiliated Kangning Hosp, Wenzhou, Zhejiang, Peoples R China
基金
中国博士后科学基金;
关键词
nerve regeneration; psychological stress; serotonin; 5-HT1A; 5-HT2A; brain-derived neurotrophic factor; neural regeneration; RAT HIPPOCAMPUS; MESSENGER-RNA; RECEPTOR; BDNF; ANXIETY; COMMUNICATION; ACTIVATION; MECHANISMS; SUBTYPES; AGONIST;
D O I
10.4103/1673-5374.191222
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Previous studies suggest that serotonin (5-HT) might interact with brain-derived neurotrophic factor (BDNF) during the stress response. However, the relationship between 5-HT and BDNF expression under purely psychological stress is unclear. In this study, one hour before psychological stress exposure, the 5-HT1A receptor agonist 8-OH-DPAT or antagonist MDL73005, or the 5-HT2A receptor agonist DOI or antagonist ketanserin were administered to rats exposed to psychological stress. Immunohistochemistry and in situ hybridization revealed that after psychological stress, with the exception of the ventral tegmental area, BDNF protein and mRNA expression levels were higher in the 5-HT1A and the 5-HT2A receptor agonist groups compared with the solvent control no-stress or psychological stress group in the CA1 and CA3 of the hippocampus, prefrontal cortex, central amygdaloid nucleus, dorsomedial hypothalamic nucleus, dentate gyrus, shell of the nucleus accumbens and the midbrain periaqueductal gray. There was no significant difference between the two agonist groups. In contrast, after stress exposure, BDNF protein and mRNA expression levels were lower in the 5-HT1A and 5-HT2A receptor antagonist groups than in the solvent control non-stress group, with the exception of the ventral tegmental area. Our findings suggest that 5-HT regulates BDNF expression in a rat model of acute psychological stress.
引用
收藏
页码:1471 / 1479
页数:9
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