Acupuncture alleviates the progression of lumbar disc herniation by regulating the autophagy level of nucleus pulposus cells through the SIRT1/Sestrin2 pathway.

IF 2.2 4区 生物学 Q3 CELL BIOLOGY
Histology and histopathology Pub Date : 2026-09-01 Epub Date: 2026-02-24 DOI:10.14670/HH-25-050
Xiaoyan Wang, Jia Lu, Pengyue Zhang, Yiming Zhang, Caiyan Li, Tao Zhang, Xianzhi Chen, Hangqi Zheng, Jie Yang, Ming Jing
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引用次数: 0

Abstract

Background and purpose: Lumbar disc herniation (LDH) is a degenerative spine disease and the most common cause of lower back pain, with a high prevalence in younger patients. The use of acupuncture (AC) as a conservative treatment for LDH has received widespread attention at home and abroad. Therefore, the present study aimed to investigate the specific mechanism of AC in the treatment of LDH.

Methods: In this study, we established an LDH rat model via autologous nucleus pulposus (NP) transplantation and treated human NP cells with 50 μM tert-butyl hydroperoxide (TBHP) for 24h to establish an LDH cell model for experimental investigation. The damage to human NP cells and the development of LDH in rats were evaluated via CCK-8, flow cytometry, H&E staining, and Safranin O-Fast Green staining, and the expression of related proteins was detected via western blotting.

Results: This study revealed that AC promoted the protein expression of Collagen II, Bcl-2, LC3II/I, and Beclin1, and inhibited the protein expression of Bax, Cleaved Caspase-3, and p62, thereby improving the pathological condition of lumbar NP tissue in rats and alleviating LDH progression. In addition, SIRT1 and Sestrin2 are expressed at low levels in LDH, and the overexpression of SIRT1 or Sestrin2 can improve NP cell viability and inhibit cell apoptosis by activating autophagy. Mechanistically, AC inhibits the MDM2-mediated ubiquitination of Sestrin2 by upregulating SIRT1 expression, thereby promoting Sestrin2 expression, activating autophagy, and ultimately alleviating the development of LDH.

Conclusion: AC relieves the development of LDH by activating the SIRT1/Sestrin2 autophagy pathway. Our study provides a new molecular mechanism for the AC treatment of LDH.

针刺通过SIRT1/Sestrin2通路调节髓核细胞自噬水平,缓解腰椎间盘突出症的进展。
背景和目的:腰椎间盘突出症(LDH)是一种退行性脊柱疾病,是引起下背部疼痛的最常见原因,在年轻患者中发病率很高。针刺作为LDH的保守治疗已受到国内外的广泛关注。因此,本研究旨在探讨AC治疗LDH的具体机制。方法:本研究通过自体髓核(NP)移植建立LDH大鼠模型,用50 μM的过氧化叔丁基(thbhp)处理人NP细胞24h,建立LDH细胞模型进行实验研究。通过CCK-8、流式细胞术、H&E染色、Safranin O-Fast Green染色评价其对人NP细胞的损伤及大鼠LDH的形成,western blotting检测相关蛋白的表达。结果:本研究发现,AC可促进Collagen II、Bcl-2、LC3II/I、Beclin1蛋白表达,抑制Bax、Cleaved Caspase-3、p62蛋白表达,从而改善大鼠腰椎NP组织病理状况,缓解LDH进展。此外,SIRT1和Sestrin2在LDH中低水平表达,过表达SIRT1或Sestrin2可以通过激活自噬来提高NP细胞活力,抑制细胞凋亡。在机制上,AC通过上调SIRT1表达抑制mdm2介导的Sestrin2泛素化,从而促进Sestrin2表达,激活自噬,最终缓解LDH的发展。结论:AC通过激活SIRT1/Sestrin2自噬通路来缓解LDH的发展。本研究为交流电治疗LDH提供了一种新的分子机制。
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
Histology and histopathology
Histology and histopathology 生物-病理学
CiteScore
3.90
自引率
0.00%
发文量
232
审稿时长
2 months
期刊介绍: HISTOLOGY AND HISTOPATHOLOGY is a peer-reviewed international journal, the purpose of which is to publish original and review articles in all fields of the microscopical morphology, cell biology and tissue engineering; high quality is the overall consideration. Its format is the standard international size of 21 x 27.7 cm. One volume is published every year (more than 1,300 pages, approximately 90 original works and 40 reviews). Each volume consists of 12 numbers published monthly online. The printed version of the journal includes 4 books every year; each of them compiles 3 numbers previously published online.
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