Sound induces analgesia through corticothalamic circuits

Author:

Zhou Wenjie1ORCID,Ye Chonghuan1ORCID,Wang Haitao23ORCID,Mao Yu14ORCID,Zhang Weijia1ORCID,Liu An5ORCID,Yang Chen-Ling5ORCID,Li Tianming6,Hayashi Lauren6ORCID,Zhao Wan7ORCID,Chen Lin2ORCID,Liu Yuanyuan6,Tao Wenjuan5ORCID,Zhang Zhi1ORCID

Affiliation:

1. Department of Anesthesiology and Pain Medicine, The First Affiliated Hospital of USTC, Hefei National Laboratory for Physical Sciences at the Microscale, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, PR China.

2. Auditory Research Laboratory, Department of Neurobiology and Biophysics, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, PR China.

3. School of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, PR China.

4. Department of Anesthesiology and Pain Management, The First Affiliated Hospital of Anhui Medical University, Hefei, PR China.

5. Department of Physiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, PR China.

6. Somatosensation and Pain Unit, National Institute of Dental and Craniofacial Research (NIDCR), National Center for Complementary and Integrative Health (NCCIH), National Institutes of Health (NIH), Bethesda, MD, USA.

7. Department of Otolaryngology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, PR China.

Abstract

Sound—including music and noise—can relieve pain in humans, but the underlying neural mechanisms remain unknown. We discovered that analgesic effects of sound depended on a low (5-decibel) signal-to-noise ratio (SNR) relative to ambient noise in mice. Viral tracing, microendoscopic calcium imaging, and multitetrode recordings in freely moving mice showed that low-SNR sounds inhibited glutamatergic inputs from the auditory cortex (ACx Glu ) to the thalamic posterior (PO) and ventral posterior (VP) nuclei. Optogenetic or chemogenetic inhibition of the ACx Glu →PO and ACx Glu →VP circuits mimicked the low-SNR sound–induced analgesia in inflamed hindpaws and forepaws, respectively. Artificial activation of these two circuits abolished the sound-induced analgesia. Our study reveals the corticothalamic circuits underlying sound-promoted analgesia by deciphering the role of the auditory system in pain processing.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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