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Abstract
Itch is an annoying sensation consisting of both sensory and emotional components. It is known to involve the parabrachial nucleus (PBN), but the following transmission nodes remain elusive. The present study identified that the PBN-central medial thalamic nucleus (CM)-medial prefrontal cortex (mPFC) pathway is essential for itch signal transmission at the supraspinal level in male mice. Chemogenetic inhibition of the CM-mPFC pathway attenuates scratching behavior or chronic itch-related affective responses. CM input to mPFC pyramidal neurons is enhanced in acute and chronic itch models. Specifically chronic itch stimuli also alter mPFC interneuron involvement, resulting in enhanced feedforward inhibition and a distorted excitatory/inhibitory balance in mPFC pyramidal neurons. The present work underscores CM as a transmit node of the itch signal in the thalamus, which is dynamically engaged in both the sensory and affective dimensions of itch with different stimulus salience.
Itch is known to involve the parabrachial nucleus, but the following transmission nodes remain elusive. Here, the authors show in male mice that the central medial thalamic nucleus—medial prefrontal cortex (mPFC) pathway transmits itch signals and is involved in both acute scratching and chronic itch-related affective behavior, with an altered excitatory/inhibitory balance in mPFC in chronic itch models.
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1 The Fourth Military Medical University, Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, Xi’an, China (GRID:grid.233520.5) (ISNI:0000 0004 1761 4404)
2 The Fourth Military Medical University, Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, Xi’an, China (GRID:grid.233520.5) (ISNI:0000 0004 1761 4404); Sichuan University, Department of Human Anatomy, West China School of Basic Medical Sciences & Forensic Medicine, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581)
3 The Fourth Military Medical University, Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, Xi’an, China (GRID:grid.233520.5) (ISNI:0000 0004 1761 4404); Zhengzhou University, Department of Anatomy, Basic Medical College, Zhengzhou, China (GRID:grid.207374.5) (ISNI:0000 0001 2189 3846)
4 The Fourth Military Medical University, Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, Xi’an, China (GRID:grid.233520.5) (ISNI:0000 0004 1761 4404); Fujian Medical University, Department of Human Anatomy, The School of Basic Medical Sciences, Fuzhou, China (GRID:grid.256112.3) (ISNI:0000 0004 1797 9307)
5 The Fourth Military Medical University, Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, Xi’an, China (GRID:grid.233520.5) (ISNI:0000 0004 1761 4404); Baotou Medical College Inner Mongolia University of Science and Technology, Department of Human Anatomy, Baotou, China (GRID:grid.462400.4) (ISNI:0000 0001 0144 9297)
6 The Fourth Military Medical University, Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, Xi’an, China (GRID:grid.233520.5) (ISNI:0000 0004 1761 4404); Sichuan University, Department of Human Anatomy, West China School of Basic Medical Sciences & Forensic Medicine, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581); Zhengzhou University, Department of Anatomy, Basic Medical College, Zhengzhou, China (GRID:grid.207374.5) (ISNI:0000 0001 2189 3846); Fujian Medical University, Department of Human Anatomy, The School of Basic Medical Sciences, Fuzhou, China (GRID:grid.256112.3) (ISNI:0000 0004 1797 9307); Baotou Medical College Inner Mongolia University of Science and Technology, Department of Human Anatomy, Baotou, China (GRID:grid.462400.4) (ISNI:0000 0001 0144 9297)