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原位成像研究单胺类递质的定位和动力学变化。

In situ imaging of monoamine localization and dynamics.

机构信息

Department of Biochemistry, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan; Laboratory of Analytical and Bio-Analytical Chemistry, School of Pharmaceutical Sciences, University of Shizuoka 52-1 Yada, Suruga-ku, Shizuoka, 422-8526, Japan.

Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Pharmacol Ther. 2020 Apr;208:107478. doi: 10.1016/j.pharmthera.2020.107478. Epub 2020 Jan 10.

Abstract

Recent advances in sample preparation protocols and instrumentation allow current imaging mass spectrometry (IMS) to enable the visualization of small molecule tissue localization, including that of monoamine neurotransmitters, such as serotonin, dopamine, and norepinephrine. Although monoamine-producing neurons, and their projections and synaptic connections, have been thoroughly characterized, in situ monoamine localization within these circuits remains unclear. Moreover, studying the fluctuations in local monoamine concentration in response to physiological stimuli, drug administration, and neurodegenerative disease progression is worthwhile, and can be achieved by analyzing the in situ concentration maps afforded by coupling IMS with on-tissue derivatization protocols. Recent reports have shown that monoamines localize within cell bodies and also translocate to distant nerve terminals, indicating active transport along axons and/or local synthesis at the terminals. Moreover, IMS can reveal regionally segregated monoamine fluctuations, such as rapid dopamine fluctuation within the nucleus accumbens (NAc) subregion during pain sensation. Furthermore, since exogenous drug pharmacokinetics can also be visualized by IMS, this technique could provide powerful methodologies enabling the simultaneous imaging of monoamines and drugs that selectively regulate monoamine signaling, such as serotonin reuptake inhibitors (SSRIs). Therefore, IMS could reveal where SSRIs administered over the long-term accumulate and how they affect local monoamine metabolism.

摘要

最近,样品制备方案和仪器的进步使得当前的成像质谱(IMS)能够可视化小分子的组织定位,包括单胺神经递质,如血清素、多巴胺和去甲肾上腺素。尽管单胺产生神经元及其投射和突触连接已经得到了彻底的描述,但这些回路中的原位单胺定位仍然不清楚。此外,研究局部单胺浓度对生理刺激、药物给药和神经退行性疾病进展的波动是有价值的,可以通过分析耦合 IMS 与组织内衍生化方案提供的原位浓度图来实现。最近的报告表明,单胺存在于细胞体中,也可以转移到遥远的神经末梢,这表明沿着轴突进行主动运输和/或在末梢处进行局部合成。此外,IMS 可以揭示区域分隔的单胺波动,例如在疼痛感觉期间,在伏隔核(NAc)亚区中快速的多巴胺波动。此外,由于 IMS 还可以可视化外源性药物药代动力学,因此该技术可以提供强大的方法,能够同时成像单胺和选择性调节单胺信号的药物,如选择性 5-羟色胺再摄取抑制剂(SSRIs)。因此,IMS 可以揭示长期给予 SSRIs 后它们积累的位置以及它们如何影响局部单胺代谢。

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