M4阳性变构调节剂VU0467154对雄性小鼠安非他明致敏和自发运动的影响。

IF 3.9 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
ACS Chemical Neuroscience Pub Date : 2025-03-05 Epub Date: 2025-02-21 DOI:10.1021/acschemneuro.4c00795
Anna Berezovskaia, Craig Lindsley, Anders Fink-Jensen, Gitta Wörtwein
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引用次数: 0

摘要

本研究探讨毒毒碱乙酰胆碱受体亚型4 (M4)阳性变构调节剂(PAM) VU0467154对小鼠安非他明致敏的发育、孵育和表达的影响,致敏诱导和表达后内侧前额叶皮层即时早期基因的表达,以及对自发运动和感觉运动功能几个方面的影响。小鼠分别在诱导期、激射试验前或同时接受VU0467154预处理。另一组患者在潜伏期接受治疗。VU0467154给药后进行自主运动和感觉运动功能测试以评估潜在副作用。VU0467154抑制了安非他明致敏性的发展和表达。这与内侧前额叶皮层中直接早期基因表达的影响是平行的。此外,先前在诱导阶段用VU0467154预处理后,两周潜伏期后敏化表达减弱。然而,在潜伏期用VU0467154处理不影响致敏反应的表达。VU0467154显著减少自发运动,而不损害感觉运动功能的其他方面,通过网格,粘合剂去除,水平条和负地向性测试进行评估。全局M4敲除小鼠证实了对自发运动的抑制作用是M4受体特有的。我们的研究结果为M4 PAMs在调节与精神兴奋剂滥用相关的神经适应性方面的治疗潜力提供了新的见解。总的来说,这些结果表明,激活M4受体可能是调节多巴胺能信号和减少与物质使用障碍相关的一些行为的一种有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
M4 Positive Allosteric Modulator VU0467154 Impacts Amphetamine Sensitization and Spontaneous Locomotion in Male Mice.

This study investigates the effects of the muscarinic acetylcholine receptor subtype 4 (M4) positive allosteric modulator (PAM) VU0467154 on the development, incubation, and expression of amphetamine sensitization in mice, the expression of immediate early genes in the medial prefrontal cortex after induction and expression of sensitization, as well as on spontaneous locomotion and several aspects of sensorimotor function. Mice were pretreated with VU0467154 during the induction phase, before the challenge test, or both. A separate cohort was treated during the incubation period. Tests of spontaneous locomotion and sensorimotor function were conducted after VU0467154 administration to evaluate potential side effects. Treatment with VU0467154 inhibited the development and expression of amphetamine sensitization. This was paralleled by effects on immediate early gene expression in the medial prefrontal cortex. Additionally, previous pretreatment with VU0467154 during the induction phase attenuated the expression of sensitization after a two-week incubation period. However, treatment with VU0467154 during the incubation period did not affect the expression of a sensitized response. VU0467154 significantly reduced spontaneous locomotion without impairing other aspects of sensorimotor function, as assessed by the mesh, adhesive removal, horizontal bar, and negative geotaxis tests. Global M4 knockout mice confirmed that the inhibitory effect on spontaneous locomotion was specific to M4 receptors. Our findings provide new insights into the therapeutic potential of M4 PAMs in modulating the neuroadaptations associated with psychostimulant abuse. Collectively, these results suggest that activation of M4 receptors could be a promising strategy for modulating dopaminergic signaling and reducing some behaviors associated with substance use disorder.

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来源期刊
ACS Chemical Neuroscience
ACS Chemical Neuroscience BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
9.20
自引率
4.00%
发文量
323
审稿时长
1 months
期刊介绍: ACS Chemical Neuroscience publishes high-quality research articles and reviews that showcase chemical, quantitative biological, biophysical and bioengineering approaches to the understanding of the nervous system and to the development of new treatments for neurological disorders. Research in the journal focuses on aspects of chemical neurobiology and bio-neurochemistry such as the following: Neurotransmitters and receptors Neuropharmaceuticals and therapeutics Neural development—Plasticity, and degeneration Chemical, physical, and computational methods in neuroscience Neuronal diseases—basis, detection, and treatment Mechanism of aging, learning, memory and behavior Pain and sensory processing Neurotoxins Neuroscience-inspired bioengineering Development of methods in chemical neurobiology Neuroimaging agents and technologies Animal models for central nervous system diseases Behavioral research
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