Electroacupuncture on GB acupoints improves osteoporosis via the estradiol-PI3K-Akt signaling pathway.

IF 1.7 4区 生物学 Q3 BIOLOGY
Open Life Sciences Pub Date : 2024-11-19 eCollection Date: 2024-01-01 DOI:10.1515/biol-2022-0978
Xinyu Wang, Xiyu Zeng, Yu Long, Yanfei Du, Chang Li, Hua Jiang, Guang Li
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引用次数: 0

Abstract

Recent studies have reported that electroacupuncture (EA) can treat osteoporosis, but most of which were based on the "kidney governing bones" theory. However, the ancient Chinese medical textbook Huangdi Neijing pointed out that "Gallbladder Meridian of Foot Shaoyang" correlates with bone diseases, including osteoporosis, although the therapeutic regimens were lost after the Tang Dynasty. Here, we explored whether EA at GB points improves osteoporosis and its underlying mechanism. We constructed ovariectomized mice and treated them with EA at GB30 (Huantiao), GB34 (Yanglingquan), and GB39 (Xuanzhong) acupoints. EA treatment significantly improved bone parameters in osteoporotic mice, as evidenced by micro-computed tomography and histological assessment. Additionally, EA treatment elevated the serum levels of estradiol and SOD that were downregulated in osteoporotic mice. Transcriptome and qPCR results verified that EA treatment upregulated the expression of genes associated with bone formation. Moreover, transcriptome analysis revealed differential enrichment of the PI3K-Akt pathway. Furthermore, Western blot analysis demonstrated that estradiol partially counteracted a reduction in p-AKT expression induced by hydrogen peroxide. These findings indicate that EA treatment increases serum estradiol levels in mice, thus inhibiting osteoporosis induced by oxidative stress. This effect is achieved by activating the PI3K-Akt signaling pathway.

电针国标穴位可通过雌二醇-PI3K-Akt 信号通路改善骨质疏松症。
近来有研究报告称,电针(EA)可治疗骨质疏松症,但这些研究大多基于 "肾主骨 "的理论。然而,中医古籍《黄帝内经》指出,"足少阳胆经 "与骨质疏松症等骨病相关,但唐代以后治疗方案已失传。在此,我们探讨了国标穴位 EA 是否能改善骨质疏松症及其内在机制。我们构建了卵巢切除的小鼠,并在国标 30(黄庭经)、国标 34(阳陵泉)和国标 39(玄中经)穴位进行 EA 治疗。通过微计算机断层扫描和组织学评估,EA 治疗可明显改善骨质疏松症小鼠的骨骼参数。此外,EA 还能提高骨质疏松症小鼠血清中雌二醇和 SOD 的水平,而这两种物质在骨质疏松症小鼠中的水平是下调的。转录组和 qPCR 结果证实,EA 治疗可上调骨形成相关基因的表达。此外,转录组分析表明,PI3K-Akt 通路的富集程度不同。此外,Western 印迹分析表明,雌二醇部分抵消了过氧化氢诱导的 p-AKT 表达的减少。这些研究结果表明,EA 治疗可提高小鼠血清中的雌二醇水平,从而抑制氧化应激诱导的骨质疏松症。这种效果是通过激活 PI3K-Akt 信号通路实现的。
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
CiteScore
2.50
自引率
4.50%
发文量
131
审稿时长
43 weeks
期刊介绍: Open Life Sciences (previously Central European Journal of Biology) is a fast growing peer-reviewed journal, devoted to scholarly research in all areas of life sciences, such as molecular biology, plant science, biotechnology, cell biology, biochemistry, biophysics, microbiology and virology, ecology, differentiation and development, genetics and many others. Open Life Sciences assures top quality of published data through critical peer review and editorial involvement throughout the whole publication process. Thanks to the Open Access model of publishing, it also offers unrestricted access to published articles for all users.
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