State of the art indicators for imaging purinergic dynamics in vitro and in vivo.

IF 3 4区 医学 Q2 NEUROSCIENCES
Yumo Li, Liwan Zhang, Bohan Li, Yulong Li, Zhaofa Wu
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引用次数: 0

Abstract

Purinergic neurotransmission, a dynamic signaling system using adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine (ADO), uridine diphosphate (UDP), and others, plays a crucial role in brain function. Purinergic signaling is involved in regulating synaptic communication to influence sleep and neuroprotection; malfunction of purinergic signaling contributes to various neurological disorders like pain, epilepsy, and depression. Effective detection methods are crucial for a comprehensive understanding of the multifaceted roles of purinergic signaling in the brain. This review sheds light on advancements in fluorescent indicators, a powerful toolkit for visualizing purinergic activities in living animals. We explore the diverse applications of these indicators in studying purinergic transmission both in health and in diseases. Despite their current strengths, we emphasize the need for continuous development of fluorescent indicators to achieve an even more comprehensive, specific, and quantitative detection of purinergic signaling.

体外和体内嘌呤能动态成像的最新技术指标。
嘌呤能神经传递是一种由三磷酸腺苷(ATP)、二磷酸腺苷(ADP)、腺苷(ADO)、二磷酸尿苷(UDP)等组成的动态信号系统,在脑功能中起着至关重要的作用。嘌呤能信号参与调节突触通讯,影响睡眠和神经保护;嘌呤能信号的功能障碍会导致各种神经系统疾病,如疼痛、癫痫和抑郁。有效的检测方法对于全面了解嘌呤能信号在大脑中的多方面作用至关重要。本文综述了荧光指示剂的研究进展,荧光指示剂是观察活体动物嘌呤能活性的有力工具。我们探索这些指标在研究嘌呤能在健康和疾病中的传播的不同应用。尽管它们目前的优势,我们强调需要不断发展荧光指标,以实现更全面,具体和定量检测嘌呤能信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
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