P2X7 and P2Y1 receptors in DRG mediate electroacupuncture to inhibit peripheral sensitization in rats with IBS visceral pain.

IF 3 4区 医学 Q2 NEUROSCIENCES
Tingting Lv, Guona Li, Chen Zhao, Jindan Ma, Fang Zhang, Min Zhao, Huirong Liu, Huangan Wu, Kunshan Li, Zhijun Weng
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引用次数: 0

Abstract

Although multiple purinergic receptors mediate the analgesic effects of acupuncture, it remains unclear whether there is mutual interaction between purinergic receptors to jointly mediate the electroacupuncture inhibition of peripheral sensitization in visceral pain. Visceral hypersensitivity was induced by intracolonic 2,4,6-trinitrobenzene sulfonic acid (TNBS) in rat. The antinociception effect of electroacupuncture on visceral pain was evaluated by morphology, behaviors, neuroelectrophysiology and molecular biology techniques. After labeling the colon-related primary sensory neurons with neural retrograde tracer and employing neuropharmacology, neuroelectrophysiology, and molecular biotechnology, the mechanisms of P2X7R, P2Y1R, and P2X3R in colon-related dorsal root ganglion (DRG) neurons alleviating visceral hypersensitivity of irritable bowel syndrome (IBS) by electroacupuncture at Zusanli and Sanyinjiao acupoints.were elucidated from the perspective of peripheral sensitization. Electroacupuncture significantly inhibited TNBS-induced colonic hypersensitivity in rats with IBS, and Satellite Glial Cells (SGCs) in DRG were found to be involved in electroacupuncture-mediated regulation of the electrophysiological properties of neurons. P2X7R was found to play a pain-inducing role in IBS visceral hypersensitivity by affecting P2X3R, and electroacupuncture exerted an analgesic effect by inhibiting P2X7R activation. P2Y1R was found to play an analgesic role in the process of visceral pain, mediating electroacupuncture to relieve visceral hypersensitivity. P2Y1R relieved visceral pain by inhibiting P2X3R in neurons associated with nociception, with P2X7R identified as upstream of P2Y1R up-regulation by electroacupuncture. Our study suggests that the P2X7R → P2Y1R → P2X3R inhibitory pathway in DRG mediates the inhibition of peripheral sensitization by electroacupuncture in rats with IBS visceral hypersensitivity.

Abstract Image

DRG中的P2X7和P2Y1受体介导电针抑制肠易激综合征内脏痛大鼠的外周敏感性
虽然多种嘌呤能受体介导了针灸的镇痛作用,但嘌呤能受体之间是否存在相互作用以共同介导电针抑制内脏痛的外周敏化作用仍不清楚。大鼠内腔注射 2,4,6-三硝基苯磺酸(TNBS)诱导内脏超敏反应。通过形态学、行为学、神经电生理学和分子生物学技术评估了电针对内脏痛的抗痛作用。用神经逆行示踪剂标记结肠相关初级感觉神经元后,运用神经药理学、神经电生理学和分子生物学技术,从电针足三里穴和三阴交穴的角度阐明了结肠相关背根神经节(DRG)神经元中的P2X7R、P2Y1R和P2X3R缓解肠易激综合征(IBS)内脏超敏反应的机制。从外周敏化的角度阐明了电针对肠易激综合征(IBS)内脏超敏反应的影响。研究发现,电针可明显抑制 TNBS 诱导的肠易激综合征大鼠结肠超敏反应,DRG 中的卫星胶质细胞(SGCs)参与了电针对神经元电生理特性的调控。研究发现 P2X7R 通过影响 P2X3R 在肠易激综合征内脏超敏反应中发挥诱导疼痛的作用,而电针通过抑制 P2X7R 的激活发挥镇痛作用。研究发现,P2Y1R 在内脏疼痛过程中发挥镇痛作用,介导电针缓解内脏超敏反应。P2Y1R 通过抑制与痛觉相关神经元中的 P2X3R 来缓解内脏疼痛,而 P2X7R 被确定为电针上调 P2Y1R 的上游。我们的研究表明,DRG 中的 P2X7R → P2Y1R → P2X3R 抑制通路介导了电针对 IBS 内脏过敏大鼠外周敏化的抑制作用。
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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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