Evidence map›Paper›PMID 41082001›Full record

ArticleApplied biochemistry and biotechnology2025

Astragalus Polysaccharides Alleviate Lumbar Disc Herniation by Promoting the O-GlcNAcylation of NRF2.

Hao Tan, Pingsen Xiao, Cao Fang, Zhi Wang

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Article in Applied biochemistry and biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hao Tan *Department of Orthopedics, Changsha Hospital of Traditional Chinese Medicine (Changsha Eighth Hospital), Changsha, 410100, Hunan, China.
Pingsen Xiao *Department of Orthopedics, Changsha Hospital of Traditional Chinese Medicine (Changsha Eighth Hospital), Changsha, 410100, Hunan, China.
Cao FangOrthopedic Rehabilitation Center, Hunan Provincial Occupational Disease Prevention and Treatment Hospital , Occupational Disease Prevention and Treatment Hospital, University of South China, Changsha, Hunan , 410100, China.
Zhi WangDepartment of Orthopedics, Changsha Hospital of Traditional Chinese Medicine (Changsha Eighth Hospital), Changsha, 410100, Hunan, China. wyh05310103@163.com.

Funding

Changsha Natural Science Foundation Project in 2024 kq2502319
6 · The paper itself

Abstract

Lumbar disc herniation (LDH) is a complex degenerative disease caused by inflammation and mechanical compression of nerve roots by the nucleus pulposus (NP). Astragalus polysaccharides (APS) have anti-inflammatory and immunomodulatory effects. Given the regulatory role of O-GlcNAcylation in inflammation and degenerative diseases, this study aimed to explore the potential molecular regulatory mechanism of O-GlcNAcylation in the anti-inflammatory effect of APS in LDH. We established the LDH rat model to investigate the effects of APS on LDH and inflammatory response. IL-1β-stimulated NP cells were generated, and inflammation was assessed by measuring the expression of IL-6, IL-18, and TNF-α with enzyme-linked immunosorbent assay. The apoptosis of NP cells was analyzed by flow cytometry. The underlying mechanism was investigated by quantitative real-time PCR, co-immunoprecipitation, and molecular docking. The results indicated that APS inhibited proinflammatory cytokine expression in LDH rats and IL-1β-induced NP cells. APS bonded to OGT and promoted its mediated-O-GlcNAcylation levels. Further, we certified that NRF2 was the target of OGT-mediated O-GlcNAcylation. Of note, the silencing of NRF2 abolished the protective effects of OGT on IL-1β-stimulated NP cells. The mitigation effect of APS on LDH is through enhancing OGT expression to promote O-GlcNAcylation of NRF2, suggesting that O-GlcNAcylation of NRF2 is an important regulatory factor for LDH and offers a novel treatment strategy for the disease.

Indexed as

Astragalus PlantIntervertebral Disc DisplacementLumbar VertebraeNF-E2-Related Factor 2PolysaccharidesAnimalsMaleMolecular Docking SimulationNucleus PulposusRatsRats, Sprague-DawleyNfe2l2 protein, ratNF-E2-Related Factor 2PolysaccharidesAstragalus polysaccharidesInflammatoryLumbar disc herniationNRF2O-GlcNAcylation

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.