调节机械性抗痛觉的吗啡反应神经元

IF 44.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Science Pub Date : 2024-08-30 DOI:10.1126/science.ado6593
Michael P. Fatt, Ming-Dong Zhang, Jussi Kupari, Müge Altınkök, Yunting Yang, Yizhou Hu, Per Svenningsson, Patrik Ernfors
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引用次数: 0

摘要

阿片类药物是治疗严重急性和慢性疼痛的广泛而有效的镇痛药,但最近由于其滥用程度达到流行病的程度而备受关注。虽然这些化合物作用于许多中枢和外周疼痛通路,但阿片类镇痛的神经解剖基底尚未完全清楚。通过单细胞转录组学和对吗啡反应神经元的操作,我们在小鼠喙侧腹膜髓质(RVM)中发现了一组神经元,它们能调节小鼠的机械痛觉。其中,通过脑源性神经营养因子(BDNF)/前肌球蛋白受体激酶 B(TrkB)依赖性机制和抑制性脊髓加兰宁阳性神经元的激活,强迫激活或沉默兴奋性 RVMBDNF 投射神经元分别模拟或完全逆转了吗啡诱导的机械性抗痛觉。我们的研究结果揭示了调节机械痛觉的特定RVM-脊髓回路,其功能赋予了吗啡抗痛觉的特性。
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Morphine-responsive neurons that regulate mechanical antinociception
Opioids are widely used, effective analgesics to manage severe acute and chronic pain, although they have recently come under scrutiny because of epidemic levels of abuse. While these compounds act on numerous central and peripheral pain pathways, the neuroanatomical substrate for opioid analgesia is not fully understood. By means of single-cell transcriptomics and manipulation of morphine-responsive neurons, we have identified an ensemble of neurons in the rostral ventromedial medulla (RVM) that regulates mechanical nociception in mice. Among these, forced activation or silencing of excitatory RVMBDNF projection neurons mimicked or completely reversed morphine-induced mechanical antinociception, respectively, via a brain-derived neurotrophic factor (BDNF)/tropomyosin receptor kinase B (TrkB)–dependent mechanism and activation of inhibitory spinal galanin-positive neurons. Our results reveal a specific RVM-spinal circuit that scales mechanical nociception whose function confers the antinociceptive properties of morphine.
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来源期刊
Science
Science 综合性期刊-综合性期刊
CiteScore
61.10
自引率
0.90%
发文量
0
审稿时长
2.1 months
期刊介绍: Science is a leading outlet for scientific news, commentary, and cutting-edge research. Through its print and online incarnations, Science reaches an estimated worldwide readership of more than one million. Science’s authorship is global too, and its articles consistently rank among the world's most cited research. Science serves as a forum for discussion of important issues related to the advancement of science by publishing material on which a consensus has been reached as well as including the presentation of minority or conflicting points of view. Accordingly, all articles published in Science—including editorials, news and comment, and book reviews—are signed and reflect the individual views of the authors and not official points of view adopted by AAAS or the institutions with which the authors are affiliated. Science seeks to publish those papers that are most influential in their fields or across fields and that will significantly advance scientific understanding. Selected papers should present novel and broadly important data, syntheses, or concepts. They should merit recognition by the wider scientific community and general public provided by publication in Science, beyond that provided by specialty journals. Science welcomes submissions from all fields of science and from any source. The editors are committed to the prompt evaluation and publication of submitted papers while upholding high standards that support reproducibility of published research. Science is published weekly; selected papers are published online ahead of print.
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