Lifespan changes in cannabinoid 1 receptor mRNA expression in the female C57BL/6J mouse brain

被引:1
作者
Li, Xulin [1 ,2 ,3 ]
Zhao, Gaoyang [1 ,2 ,3 ]
Huang, Hongren [1 ,2 ,3 ]
Ye, Jialin [1 ,2 ,3 ]
Xu, Junfeng [1 ,2 ,3 ]
Zhou, Yuan [1 ,2 ,3 ]
Zhu, Xiaojuan [4 ]
Wang, Liping [1 ,2 ]
Wang, Feng [1 ,2 ]
机构
[1] Chinese Acad Sci, Guangdong Prov Key Lab Brain Connectome & Behav, Shenzhen Inst Adv Technol,Shenzhen Key Lab Transl, CAS Key Lab Brain Connectome & Manipulat,Brain Co, Shenzhen 518055, Peoples R China
[2] Shenzhen Hong Kong Inst Brain Sci Shenzhen Fundam, Shenzhen 518055, Peoples R China
[3] Univ Chinese Acad Sci, Beijing, Peoples R China
[4] Northeast Normal Univ, Inst Genet & Cytol, Key Lab Mol Epigenet, Minist Educ, Changchun, Peoples R China
基金
中国国家自然科学基金;
关键词
cannabinoid; 1; receptor; female brain; maturation and aging; ENDOCANNABINOID SYSTEM; SEX-DIFFERENCES; CB1; RECEPTOR; BINDING; NEURONS; AGE; MODEL; GABA; HETEROGENEITY; HYPOTHALAMUS;
D O I
10.1002/cne.25427
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Many brain functions that underlie behavior, cognition, and emotions vary with age, as does susceptibility to neuropsychological disorders. The expression of specific genes that are involved in these functions, such as the genes encoding for oxytocin, its receptors, and apolipoprotein D, varies with age across different brain regions. The cannabinoid 1 receptor (CB1R) is one of the most widely spread G-protein coupled receptors in the central nervous system and is increasingly recognized for its important contribution to various brain functions. Although changes in CB1R expression with age have been reported in the male mouse brain, they have not been well investigated in the female brain. Here, we used fluorescence in situ hybridization to target CB1R mRNA in the whole brains of female C57BL/6J mice aged 4, 6, 12, 52 (12 months) and 86 weeks (20 months), and quantified CB1R-positive cells in 36 brain regions across the whole brain. The results showed that CB1R-positive cells number changed with age. Specifically, CB1R expression increased with age in some subregions of the cortex, decreased with age in the lateral septal area, and reached its lowest level at 52 weeks in the thalamus, hypothalamus, and hindbrain subregions. Cluster analysis revealed that some brain regions shared similar temporal characteristics in CB1R-positive cell number across the lifespan. Our results provide evidence that investigation of the neural basis of age-related characteristics of female brain functions is not only warranted but required.
引用
收藏
页码:294 / 313
页数:20
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