Literature DB >> 32412932

Dexmedetomidine Activation of Dopamine Neurons in the Ventral Tegmental Area Attenuates the Depth of Sedation in Mice.

Gaolin Qiu1, Ying Wu, Zeyong Yang, Long Li, Xiaona Zhu, Yiqiao Wang, Wenzhi Sun, Hailong Dong, Yuanhai Li, Ji Hu.   

Abstract

BACKGROUND: Dexmedetomidine induces a sedative response that is associated with rapid arousal. To elucidate the underlying mechanisms, the authors hypothesized that dexmedetomidine increases the activity of dopaminergic neurons in the ventral tegmental area, and that this action contributes to the unique sedative properties of dexmedetomidine.
METHODS: Only male mice were used. The activity of ventral tegmental area dopamine neurons was measured by a genetically encoded Ca indicator and patch-clamp recording. Dopamine neurotransmitter dynamics in the medial prefrontal cortex and nucleus accumbens were measured by a genetically encoded dopamine sensor. Ventral tegmental area dopamine neurons were inhibited or activated by a chemogenetic approach, and the depth of sedation was estimated by electroencephalography.
RESULTS: Ca signals in dopamine neurons in the ventral tegmental area increased after intraperitoneal injection of dexmedetomidine (40 μg/kg; dexmedetomidine, 16.917 [14.882; 21.748], median [25%; 75%], vs. saline, -0.745 [-1.547; 0.359], normalized data, P = 0.001; n = 6 mice). Dopamine transmission increased in the medial prefrontal cortex after intraperitoneal injection of dexmedetomidine (40 μg/kg; dexmedetomidine, 10.812 [9.713; 15.104], median [25%; 75%], vs. saline, -0.498 [-0.664; -0.355], normalized data, P = 0.001; n = 6 mice) and in the nucleus accumbens (dexmedetomidine, 8.543 [7.135; 11.828], median [25%; 75%], vs. saline, -0.329 [-1.220; -0.047], normalized data, P = 0.001; n = 6 mice). Chemogenetic inhibition or activation of ventral tegmental area dopamine neurons increased or decreased slow waves, respectively, after intraperitoneal injection of dexmedetomidine (40 μg/kg; delta wave: two-way repeated measures ANOVA, F[2, 33] = 8.016, P = 0.002; n = 12 mice; theta wave: two-way repeated measures ANOVA, F[2, 33] = 22.800, P < 0.0001; n = 12 mice).
CONCLUSIONS: Dexmedetomidine activates dopamine neurons in the ventral tegmental area and increases dopamine concentrations in the related forebrain projection areas. This mechanism may explain rapid arousability upon dexmedetomidine sedation. : WHAT WE ALREADY KNOW ABOUT THIS TOPIC: Dexmedetomidine is a highly selective α2 receptor agonist with unique sedative propertiesDopaminergic neurons in the ventral tegmental area express α2 receptors, and activation of these cells induces recovery from anesthesiaThe effects of dexmedetomidine on dopaminergic neurons of the ventral tegmental area are incompletely understood WHAT THIS ARTICLE TELLS US THAT IS NEW: Dexmedetomidine, via α2 receptor-dependent mechanisms, induces activation of dopaminergic neurons in the ventral tegmental area of adult miceChemogenetic approaches together with electroencephalographic recordings reveal that the activation of dopaminergic neurons in the ventral tegmental area may contribute to rapid arousability during dexmedetomidine sedation.

Entities:  

Year:  2020        PMID: 32412932     DOI: 10.1097/ALN.0000000000003347

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  6 in total

1.  Dopaminergic Neurons in the Ventral Tegmental-Prelimbic Pathway Promote the Emergence of Rats from Sevoflurane Anesthesia.

Authors:  Yanping Song; Ruitong Chu; Fuyang Cao; Yanfeng Wang; Yanhong Liu; Jiangbei Cao; Yongxin Guo; Weidong Mi; Li Tong
Journal:  Neurosci Bull       Date:  2021-12-26       Impact factor: 5.271

2.  Preliminary evaluation of the efficacy and safety of brimonidine for general anesthesia.

Authors:  Chen Bin; Wang Xiaohui; Shi Mengrou; Li Xin; Zhang Ting; Gao Ping
Journal:  BMC Anesthesiol       Date:  2021-12-03       Impact factor: 2.217

3.  High-resolution relaxometry-based calibrated fMRI in murine brain: Metabolic differences between awake and anesthetized states.

Authors:  Mengyang Xu; Binshi Bo; Mengchao Pei; Yuyan Chen; Christina Y Shu; Qikai Qin; Lydiane Hirschler; Jan M Warnking; Emmanuel L Barbier; Zhiliang Wei; Hanzhang Lu; Peter Herman; Fahmeed Hyder; Zhi-Jie Liu; Zhifeng Liang; Garth J Thompson
Journal:  J Cereb Blood Flow Metab       Date:  2021-12-15       Impact factor: 6.960

Review 4.  Neural Substrates for the Regulation of Sleep and General Anesthesia.

Authors:  Qianzi Yang; Fang Zhou; Ao Li; Hailong Dong
Journal:  Curr Neuropharmacol       Date:  2022       Impact factor: 7.708

Review 5.  Regulation of Neural Circuitry under General Anesthesia: New Methods and Findings.

Authors:  Kai Zhang; Jiacheng Pan; Yonghao Yu
Journal:  Biomolecules       Date:  2022-06-28

6.  Cell-type-specific imaging of neurotransmission reveals a disrupted excitatory-inhibitory cortical network in isoflurane anaesthesia.

Authors:  Juan Guo; Mingzi Ran; Zilong Gao; Xinxin Zhang; Dan Wang; Huiming Li; Shiyi Zhao; Wenzhi Sun; Hailong Dong; Ji Hu
Journal:  EBioMedicine       Date:  2021-03-07       Impact factor: 8.143

  6 in total

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