Selective corticofugal modulation on sound processing in auditory thalamus of awake marmosets

Author:

Wang Xiaohui1,Zhang Yuanqing1,Zhu Lin1,Bai Siyi1,Li Rui1,Sun Hao1,Qi Runze1,Cai Ruolan1,Li Min2,Jia Guoqiang1,Cao Xinyuan1,Schriver Kenneth E3ORCID,Li Xinjian14ORCID,Gao Lixia14ORCID

Affiliation:

1. Department of Neurology of the Second Affiliated Hospital , College of Biomedical Engineering and Instrument Science, Interdisciplinary Institute of Neuroscience and Technology, Zhejiang University, School of Medicine, Zhejiang University, 268 Kaixuan Road, Science Building, Room 206, Hangzhou, Zhejiang 310020 , China

2. Division of Psychology , State Key Laboratory of Cognitive Neuroscience and Learning and IDG/McGovern Institute for Brain Research, Beijing Normal University, No.19, Xinjiekouwai St, Haidian District, Beijing 100875 , China

3. School of Brain Science and Brain Medicine , Zhejiang University School of Medicine, Hangzhou 310020 , China

4. Department of Neurobiology , NHC and CAMS Key Laboratory of Medical Neurobiology, School of Brain Science and Brain Medicine, and MOE Frontier Science Center for Brain Science and Brain-machine Integration, Zhejiang University School of Medicine, Hangzhou 310020 , China

Abstract

Abstract Cortical feedback has long been considered crucial for the modulation of sensory perception and recognition. However, previous studies have shown varying modulatory effects of the primary auditory cortex (A1) on the auditory response of subcortical neurons, which complicate interpretations regarding the function of A1 in sound perception and recognition. This has been further complicated by studies conducted under different brain states. In the current study, we used cryo-inactivation in A1 to examine the role of corticothalamic feedback on medial geniculate body (MGB) neurons in awake marmosets. The primary effects of A1 inactivation were a frequency-specific decrease in the auditory response of most MGB neurons coupled with an increased spontaneous firing rate, which together resulted in a decrease in the signal-to-noise ratio. In addition, we report for the first time that A1 robustly modulated the long-lasting sustained response of MGB neurons, which changed the frequency tuning after A1 inactivation, e.g. some neurons are sharper with corticofugal feedback and some get broader. Taken together, our results demonstrate that corticothalamic modulation in awake marmosets serves to enhance sensory processing in a manner similar to center-surround models proposed in visual and somatosensory systems, a finding which supports common principles of corticothalamic processing across sensory systems.

Funder

National Natural Science Foundation of China

Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

Reference82 articles.

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