Literature DB >> 34244603

Age-dependent alterations in key components of the nigrostriatal dopaminergic system and distinct motor phenotypes.

Jiang-Peng Fan1, Hui-Zhen Geng2,3, Ya-Wei Ji2,3, Tao Jia2,3, Jennifer B Treweek4, An-An Li1, Chun-Yi Zhou5,6,7, Viviana Gradinaru4, Cheng Xiao8,9,10.   

Abstract

The nigrostriatal dopaminergic (DA) system, which includes DA neurons in the ventral and dorsal tiers of the substantia nigra pars compacta (vSNc, dSNc) and DA terminals in the dorsal striatum, is critically implicated in motor control. Accumulating studies demonstrate that both the nigrostriatal DA system and motor function are impaired in aged subjects. However, it is unknown whether dSNc and vSNc DA neurons and striatal DA terminals age in similar patterns, and whether these changes parallel motor deficits. To address this, we performed ex vivo patch-clamp recordings in dSNc and vSNc DA neurons, measured striatal dopamine release, and analyzed motor behaviors in rodents. Spontaneous firing in dSNc and vSNc DA neurons and depolarization-evoked firing in dSNc DA neurons showed inverse V-shaped changes with age. But depolarization-evoked firing in vSNc DA neurons increased with age. In the dorsal striatum, dopamine release declined with age. In locomotor tests, 12-month-old rodents showed hyperactive exploration, relative to 6- and 24-month-old rodents. Additionally, aged rodents showed significant deficits in coordination. Elevating dopamine levels with a dopamine transporter inhibitor improved both locomotion and coordination. Therefore, key components in the nigrostriatal DA system exhibit distinct aging patterns and may contribute to age-related alterations in locomotion and coordination.
© 2021. The Author(s), under exclusive licence to CPS and SIMM.

Entities:  

Keywords:  aging; coordination; dopamine sensor; dopaminergic neurons; locomotion; rodent; substantia nigra pars compacta

Mesh:

Substances:

Year:  2021        PMID: 34244603      PMCID: PMC8975991          DOI: 10.1038/s41401-021-00713-5

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  56 in total

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