Nicotine-induced transcriptional changes and mitochondrial dysfunction in the ventral tegmental area revealed by single-nucleus transcriptomics

Nicotine is widely recognized as the primary contributor to tobacco dependence. Previous studies have indicated that molecular and behavioral responses to nicotine are primarily mediated by ventral tegmental area (VTA) neurons, and accumulating evidence suggests that glia play prominent roles in nicotine addiction. However, VTA neurons and glia have yet to be characterized at the transcriptional level during the progression of nicotine self-administration. Here, a male mouse model of nicotine self-administration is established and the timing of three critical phases (pre-addiction, addicting, and post-addiction phase) is characterized. Single-nucleus RNA sequencing in the VTA at each phase is performed to comprehensively classify specific cell subtypes. Adaptive changes occurred during the addicting and post-addiction phases, with the addicting phase displaying highly dynamic neuroplasticity that profoundly impacts the transcription in each cell subtype. Furthermore, significant transcriptional changes in energy metabolism-related genes are observed, accompanied by notable structural alterations in neuronal mitochondria during the progression of nicotine self-administration. The results provide insights into mechanisms underlying the progression of nicotine addiction, serving as an important resource for identifying potential molecular targets for nicotine cessation.

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Publication Details

Journal
Journal of genetics and genomics/Journal of Genetics and Genomics
Published
2024-09-06
DOI
https://doi.org/10.1016/j.jgg.2024.08.009
Citations
4
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
1.31
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article

Nicotine-induced transcriptional changes and mitochondrial dysfunction in the ventral tegmental area revealed by single-nucleus transcriptomics

Hongwei Hou, Xia Gao, Hongjuan Wang, Sanjie Jiang et al.
4 citations
Journal of genetics and genomics/Journal of Genetics and Genomics
Adipose Tissue and Metabolism
1.31
article

Nicotine-induced transcriptional changes and mitochondrial dysfunction in the ventral tegmental area revealed by single-nucleus transcriptomics

Hongwei Hou, Xia Gao, Hongjuan Wang, Sanjie Jiang, Yong Liu, Qingyuan Hu, Fan Lei, Boxin Liu, Huan Chen, Xiaomin Zheng, Ru Yao
article en
4 citations

Abstract

Nicotine is widely recognized as the primary contributor to tobacco dependence. Previous studies have indicated that molecular and behavioral responses to nicotine are primarily mediated by ventral tegmental area (VTA) neurons, and accumulating evidence suggests that glia play prominent roles in nicotine addiction. However, VTA neurons and glia have yet to be characterized at the transcriptional level during the progression of nicotine self-administration. Here, a male mouse model of nicotine self-administration is established and the timing of three critical phases (pre-addiction, addicting, and post-addiction phase) is characterized. Single-nucleus RNA sequencing in the VTA at each phase is performed to comprehensively classify specific cell subtypes. Adaptive changes occurred during the addicting and post-addiction phases, with the addicting phase displaying highly dynamic neuroplasticity that profoundly impacts the transcription in each cell subtype. Furthermore, significant transcriptional changes in energy metabolism-related genes are observed, accompanied by notable structural alterations in neuronal mitochondria during the progression of nicotine self-administration. The results provide insights into mechanisms underlying the progression of nicotine addiction, serving as an important resource for identifying potential molecular targets for nicotine cessation.

Journal of genetics and genomics/Journal of Genetics and GenomicsVol. 51(11)
BGI Group (China) (CN), University of Science and Technology of China (CN), China Tobacco (CN), Hefei Institutes of Physical Science (CN), Tobacco Research Institute (CN), Anhui Institute of Optics and Fine Mechanics (CN)
Zero hunger
Openalex Percentile: Top 19%
Adipose Tissue and Metabolism
1.31
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