Glutamatergic neurons in thalamic paraventricular nucleus may be involved in the regulation of abnormal sleep behavior of <i>Shank3</i> gene knockout mice.

Chang-Feng CHEN; Lie-Cheng WANG; Yong LIU; Lei CHEN

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Glutamatergic neurons in thalamic paraventricular nucleus may be involved in the regulation of abnormal sleep behavior of Shank3 gene knockout mice.

Author: Chang-Feng CHEN ¹ ; Lie-Cheng WANG ¹ ; Yong LIU ² ; Lei CHEN ²
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1. School of Basic Medicine Sciences, Anhui Medical University, Hefei 230032, China.
2. Department of Pharmacy, First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230031, China.
Publication Type:Journal Article
MeSH: Animals; Mice, Knockout; Mice; Neurons/metabolism*; Nerve Tissue Proteins/physiology*; Male; Midline Thalamic Nuclei/cytology*; Circadian Rhythm/physiology*; Sleep/physiology*; Anxiety/physiopathology*; Proto-Oncogene Proteins c-fos/metabolism*; Vesicular Glutamate Transport Protein 2/metabolism*; Mice, Inbred C57BL; Microfilament Proteins
From: Acta Physiologica Sinica 2025;77(5):792-800
CountryChina
Language:Chinese
Abstract: The purpose of this study was to investigate the anxiety-like behaviors, circadian rhythms and sleep, and to elucidate the possible underlying mechanisms of the abnormal sleep behavior in Shank3 gene knockout (Shank3-KO) mice. The anxiety-like behaviors were detected by elevated plus-maze (EPM) test, open field test (OFT) and tail suspension test (TST). The circadian rhythms were detected by running wheel test. The electroencephalogram (EEG)/electromyogram (EMG) recordings were performed synchronically by polysomnograph. The distribution of SHANK3 in anterior cingulate cortex (ACC), paraventricular thalamus (PVT), nucleus accumbens (NAc), basolateral amygdala (BLA) and hippocampal CA2 region in wild type (WT) mice was detected by immunofluorescence assay. The protein expression of c-Fos in PVT, ACC and NAc was also detected by immunofluorescence assay during light cycle. The colocalization of c-Fos and vesicular glutamate transporter 2 (Vglut2, a marker for glutamatergic neurons) in the PVT was detected by immunofluorescence double labeling experiment. The results of EPM test showed that, compared with the WT mice, the Shank3-KO mice showed less time in open arms and less number of open arm entries. The results of OFT showed that the Shank3-KO mice showed less time in central area and less number of central area entries. The immobility time of Shank3-KO mice was increased in the TST. The results of running wheel rhythm test showed that the phase shift time of Shank3-KO mice in the continuous dark period was increased. The results of EEG/EMG recording showed that, compared with the WT mice, the duration of wakefulness in Shank3-KO mice was increased and the duration of non-rapid eye movement (NREM) sleep was decreased during light phase; The bout number of wakefulness was increased, the bout number of NREM sleep was decreased, NREM-wake transitions were increased, and wake-NREM transitions were decreased during light phase. SHANK3 was expressed in ACC, PVT, NAc and BLA in the WT mice. The expression of c-Fos in the PVT of Shank3-KO mice was up-regulated 2 h after entering the light phase, and majority of c-Fos was co-localized with Vglut2. These results suggest that the anxiety level of Shank3-KO mice is increased, the regulation of the internal rhythms is decreased, and the bout number of wakefulness is increased during light phase. The glutamatergic neurons in PVT may be involved in the regulation of abnormal sleep behavior in Shank3-KO mice during the light phase.