
Brief intro:
- Author: Wei Zhao, Si-Le Liu, Si-Si Lin, Ying Zhang & Chang Yu
- Journal: Purinergic Signalling
- Doi: https://www.doi.org/10.1007/s11302-024-10043-w
- Publication Date: 2024 Sep 2
Products/Services used in the paper
Quotation shows PackGene:The following virus was applied to suppress P2X7R on astrocytes: ssAAV-GFAP-mir30shRNA(mP2X7)-WPRE-SV40pA (titer: 1 × 1012GC/mL, AAV8, all from PackGene Biotech, China).
Research Field:retrosplenial cortex
AAV Serotype:AAV8
Targeted organ:left hind paw
Animal or cell line strain:mice
Abstract
P2X7 receptor (P2X7R) has been found to contribute to the peripheral mechanism of acupuncture analgesia (AA). However, whether it plays an important role in central mechanism remains unknown. In this study, we aimed to reveal the role of astrocytic P2X7R in retrosplenial cortex (RSC) in AA and provide new evidence for underlying the central mechanism of AA. We applied the chemogenetic receptors hM3Dq to stimulate or hM4Di to inhibit astrocytes ligand clozapine-N-oxide (CNO) following injection of adeno-associated virus (AAV) into the bilateral RSC, or pharmacologically intervened in the activity of the purinergic receptor P2X7R. Current data indicated that chemogenetic inhibition of astrocytes or injection of P2X7R agonist Bz-ATP in the bilateral RSC significantly reverses the analgesic effect of electroacupuncture (EA) in formalin tests while the bilateral injection of the P2X7R antagonist A438079 alleviated formalin-induced nociceptive behavior. Additionally, chemogenetic suppression of astrocytic P2X7R by injection of AAV in the bilateral RSC decreased hind paw flinches induced by formalin in the mice. These findings indicate the participation of both astrocytes and P2X7R in the RSC in EA analgesic. Moreover, P2X7R on astrocytes in the RSC appears to play a critical role in the ability of EA to attenuate formalin-induced pain responses in mice.
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