{"title":"Anatomical pathways and functional implications of the rodent auditory system-basal ganglia interconnectivity.","authors":"Ryohei Tomioka, Makoto Takemoto, Wen-Jie Song","doi":"10.3389/fnbeh.2025.1645035","DOIUrl":null,"url":null,"abstract":"<p><p>Sound influences motor functions and sound perception is conversely modulated by locomotion. Accumulating evidence supports an interconnection between the auditory system and the basal ganglia (BG), which has functional implications on the interaction between the two systems. Substantial evidence now supports auditory cortex and auditory thalamus inputs to the tri-laminar region of the tail of the striatum (tTS) in rodents. Thalamic input modulates the response gain of striatal neurons, whereas cortical input shapes their frequency tuning. Only recently has our understanding of BG projections to the auditory system advanced. GABAergic neurons in the tTS, which receive input from the auditory cortex, project to the posterior globus pallidus external segment (GPe). Posterior GPe, in turn, sends strong GABAergic projections to the non-lemniscal auditory thalamus (NLAT) and moderate projections to the cuneiform nucleus (CnF). The BG and auditory system are thus interconnected at multiple levels, forming a loop circuit in which the auditory system projects to the striatum and receives BG output via the NLAT. This circuit may mediate BG influence on auditory processing; however, the absence of motor cortex input to the tTS raises questions about its role in movement-related modulation of auditory responses. Given that the NLAT serves as a neural substrate for sound-cued aversive associative learning, BG output to the NLAT may influence learning processes. The pathway connecting the auditory system and CnF via the BG may underlie rhythmic entrainment in healthy individuals and therapeutic effects of rhythmic cues on gait in Parkinson's disease.</p>","PeriodicalId":12368,"journal":{"name":"Frontiers in Behavioral Neuroscience","volume":"19 ","pages":"1645035"},"PeriodicalIF":2.9000,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12411530/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Behavioral Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnbeh.2025.1645035","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Sound influences motor functions and sound perception is conversely modulated by locomotion. Accumulating evidence supports an interconnection between the auditory system and the basal ganglia (BG), which has functional implications on the interaction between the two systems. Substantial evidence now supports auditory cortex and auditory thalamus inputs to the tri-laminar region of the tail of the striatum (tTS) in rodents. Thalamic input modulates the response gain of striatal neurons, whereas cortical input shapes their frequency tuning. Only recently has our understanding of BG projections to the auditory system advanced. GABAergic neurons in the tTS, which receive input from the auditory cortex, project to the posterior globus pallidus external segment (GPe). Posterior GPe, in turn, sends strong GABAergic projections to the non-lemniscal auditory thalamus (NLAT) and moderate projections to the cuneiform nucleus (CnF). The BG and auditory system are thus interconnected at multiple levels, forming a loop circuit in which the auditory system projects to the striatum and receives BG output via the NLAT. This circuit may mediate BG influence on auditory processing; however, the absence of motor cortex input to the tTS raises questions about its role in movement-related modulation of auditory responses. Given that the NLAT serves as a neural substrate for sound-cued aversive associative learning, BG output to the NLAT may influence learning processes. The pathway connecting the auditory system and CnF via the BG may underlie rhythmic entrainment in healthy individuals and therapeutic effects of rhythmic cues on gait in Parkinson's disease.
期刊介绍:
Frontiers in Behavioral Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the neural mechanisms underlying behavior. Field Chief Editor Nuno Sousa at the Instituto de Pesquisa em Ciências da Vida e da Saúde (ICVS) is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
This journal publishes major insights into the neural mechanisms of animal and human behavior, and welcomes articles studying the interplay between behavior and its neurobiological basis at all levels: from molecular biology and genetics, to morphological, biochemical, neurochemical, electrophysiological, neuroendocrine, pharmacological, and neuroimaging studies.