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绘制伤害性刺激期间吗啡对腹侧被盖区的镇痛作用:一种神经病理性疼痛模型中的新型显微成像方法。

Mapping Morphine's Antinociceptive Impact on the Ventral Tegmental Area During Nociceptive Stimulation: A Novel Microimaging Approach in a Neuropathic Pain Model.

作者信息

Ganaway Austin, Kamata Airi, Yao Dunyan, Sakoori Kazuto, Okada Ryoma, Chen Ting, Ohta Yasumi, Ohta Jun, Ohsawa Masahiro, Akay Metin, Akay Yasemin M

机构信息

Biomedical Engineering Department, University of Houston, 3517 Cullen Blvd, Houston, TX 77204, USA.

Laboratory of Systems Pharmacology, Faculty of Pharmaceutical Sciences, Teikyo University, Tokyo 173-8605, Japan.

出版信息

Int J Mol Sci. 2025 Jul 7;26(13):6526. doi: 10.3390/ijms26136526.

Abstract

The neurobiology of chronic pain is complex and multifaceted, intertwining with the mesocorticolimbic system to regulate the behavioral and perceptional response to adverse stimuli. Specifically, the ventral tegmental area (VTA), the dopaminergic hub of the reward pathways located deep within the midbrain, is crucial for regulating the release of dopamine (DA) throughout the central nervous system (CNS). To better understand the nuances among chronic pain, VTA response, and therapeutics, implementing progressive approaches for mapping and visualizing the deep brain in real time during nociceptive stimulation is crucial. In this study, we utilize a fluorescence imaging platform with a genetically encoded calcium indicator (GCaMP6s) to directly visualize activity in the VTA during acute nociceptive stimulation in both healthy adult mice and adult mice with partial nerve ligation (PNL)-induced neuropathic pain. We also investigate the visualization of the analgesic properties of morphine. Deep brain imaging using our self-fabricated µ-complementary metal-oxide-semiconductor (CMOS) imaging device allows the tracking of the VTA's response to adverse stimuli. Our findings show that nociceptive stimulation is associated with a reduction in VTA fluorescence activity, supporting the potential of this platform for visualizing pain-related responses in the central nervous system. Additionally, treatment with morphine significantly reduces the neuronal response caused by mechanical stimuli and is observable using the CMOS imaging platform, demonstrating a novel way to potentially assess and treat neuropathic pain.

摘要

慢性疼痛的神经生物学复杂且多面,与中脑皮质边缘系统相互交织,以调节对不良刺激的行为和感知反应。具体而言,腹侧被盖区(VTA)是位于中脑深处的奖赏通路的多巴胺能中枢,对于调节多巴胺(DA)在整个中枢神经系统(CNS)中的释放至关重要。为了更好地理解慢性疼痛、VTA反应和治疗方法之间的细微差别,在伤害性刺激期间实时实施渐进式的深部脑图谱绘制和可视化方法至关重要。在本研究中,我们利用带有基因编码钙指示剂(GCaMP6s)的荧光成像平台,直接观察健康成年小鼠和部分神经结扎(PNL)诱导的神经性疼痛成年小鼠在急性伤害性刺激期间VTA中的活动。我们还研究了吗啡镇痛特性的可视化。使用我们自行制造的µ互补金属氧化物半导体(CMOS)成像设备进行深部脑成像,可以追踪VTA对不良刺激的反应。我们的研究结果表明,伤害性刺激与VTA荧光活性降低有关,这支持了该平台在可视化中枢神经系统中疼痛相关反应方面的潜力。此外,吗啡治疗可显著降低机械刺激引起的神经元反应,并且使用CMOS成像平台可以观察到,这展示了一种潜在评估和治疗神经性疼痛的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6640/12250161/1974055b0e2a/ijms-26-06526-g001.jpg

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