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Afferent and efferent projections of the rostral anterior cingulate cortex in young and middle-aged mice.

Authors :
Xinyi Ma
Wei Yu
Ping’an Yao
Yichen Zhu
Jiale Dai
Xiaofen He
Boyu Liu
Chi Xu
Xiaomei Shao
Jianqiao Fang
Zui Shen
Source :
Frontiers in Aging Neuroscience; 8/17/2022, Vol. 14, p1-13, 13p
Publication Year :
2022

Abstract

Research shows that across life, the incidence of mental illness is highest in the young. In the context of the COVID-19 pandemic, mental health issues of the young in particular have received global attention. The rostral anterior cingulate cortex (rACC) plays an important role in psychiatric disorders and chronic pain-psychiatric comorbidities. However, it remains unknown whether or how the afferent and efferent circuits of the rACC change with aging. In this study, we microinjected a retrograde tracer virus and an anterograde trans-monosynaptic virus into the rACC of young and middleaged mice (both male and female), and systematically and quantitatively analyzed the whole-brain afferent and efferent connections of rACC at different ages and sexes. Notably, in young and middle-aged mice, afferents of the rACC belong to four groups of brain structures arising mainly from the amygdala [mainly basolateral amygdaloid nucleus (BLA)] and cerebral cortex (mainly orbital cortex), with a small part originating from the basal forebrain and thalamus. In contrast, efferents of the rACC belong to four groups of brain structures mainly projecting to the thalamus (mainly ventral anteriorlateral/ ventromedial thalamic nucleus (VAL/VM)], with a very small part projecting to the amygdala, basal forebrain, and cerebral cortex. Compared with young mice, the BLA-rACC circuit in middle-aged mice (male and female) did not change significantly, while the rACC-VAL/VM circuit in middle-aged mice (male and female) decreased significantly. In conclusion, this study comprehensively analyzed the input-output neural projections of rACC in mice of different ages and sexes and provided preliminary evidence for further targeted research. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16634365
Volume :
14
Database :
Complementary Index
Journal :
Frontiers in Aging Neuroscience
Publication Type :
Academic Journal
Accession number :
158864369
Full Text :
https://doi.org/10.3389/fnagi.2022.960868