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RESEARCH PAPER / 2025-05-27

Upregulation of SIRT1 ameliorates apoptosis of rat nucleus pulposus cells under oxidative stress through FoxO1/β-catenin pathway.

Hongtao Hu, Sheng Wang, Haijun Teng, Sishun Zhao, Weisheng Hong

Department of Spine Surgery, Affiliated Hospital of Shandong Second Medical University, Weifang, China. · pubmed

Abstract

Age-related degenerative changes in intervertebral discs (IVDs) can lead to lower back pain, and even paralysis. This topic is therefore garnering growing attention in an increasingly ageing society. The oxidative stress-induced degenerative process is a major contributor to apoptosis in nucleus pulposus cells. However, the regulatory mechanism of NAD-dependent protein deacetylase Sirtuin-1 (SIRT1) on apoptosis in oxidative stress-induced rat nucleus pulposus cells remains unclear.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper claims that upregulation of SIRT1 can reduce apoptosis in rat nucleus pulposus cells under oxidative stress through the FoxO1/β-catenin pathway. This research is relevant as it explores a potential mechanism to mitigate age-related degeneration in intervertebral discs, addressing a root cause of aging-related issues such as lower back pain.

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