Hyperoside ameliorates neuropathic pain by modulating the astroglial reactivity in the vlPAG.

IF 4.6 2区 医学 Q1 NEUROSCIENCES Neuropharmacology Pub Date : 2025-03-15 Epub Date: 2024-12-21 DOI:10.1016/j.neuropharm.2024.110276
Tianchi Gao, Chenghao Wang, Xiaotong Yang, Zhiwei He, Yanqing Wang, Wenli Mi
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Abstract

Hyperoside, a natural flavonoid, exhibits a wide range of biological activities, including analgesic effects on acute and chronic inflammatory pain. This study illustrates that repeated intraperitoneal administration or microinjection of hyperoside into the ventrolateral periaqueductal grey (vlPAG) alleviated mechanical allodynia, cold allodynia, and abnormal gait induced by spared nerve injury (SNI) in male mice. Furthermore, repeated hyperoside administration suppressed SNI-induced astrocyte reactivity in the vlPAG. Moreover, hyperoside alleviated the pain behaviors resulting from the pharmacogenetic activation of vlPAG astrocytes. These results suggest that hyperoside may effectively mitigate neuropathic pain and inhibit astroglial reactivity in the vlPAG, highlighting its potential as a viable therapeutic intervention for chronic neuropathic pain.

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金丝桃苷通过调节vlPAG星形胶质细胞的反应性来改善神经性疼痛。
金丝桃苷是一种天然的类黄酮,具有广泛的生物活性,包括对急慢性炎症性疼痛的镇痛作用。本研究表明,反复腹腔注射或微注射金桃苷到腹侧导尿管周围灰质(vlPAG)可减轻雄性小鼠由神经损伤(SNI)引起的机械性异位痛、冷性异位痛和步态异常。此外,重复给药金丝桃苷抑制了sni诱导的vlPAG星形胶质细胞的反应性。此外,金丝桃苷可减轻vlPAG星形胶质细胞的药理学激活引起的疼痛行为。这些结果表明金丝桃苷可以有效减轻神经性疼痛并抑制vlPAG中的星形胶质细胞反应性,突出了其作为慢性神经性疼痛的可行治疗干预措施的潜力。
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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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