Evidence map›Paper›PMID 41446485›Full record

ArticleCureus2025

Moxibustion Regulates Amino Acid Metabolism Pathways to Improve Cartilage Damage in Knee Osteoarthritis Model Rats.

Liu Lei, Wei Xia, Gao Zi Zhan, Duan Wen Xiu, Yu Qing, Wang Jie, Cai Rong Lin, Wu Zi Jian

Abstract read
In one paragraph

Article in Cureus, 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.

2 · The registry

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3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Liu LeiSchool of Acupuncture and Moxibustion and Massage, Anhui University of Chinese Medicine, Hefei, CHN.
Wei XiaCollege of Traditional Chinese Medicine, Hubei College of Chinese Medicine, Jingzhou, CHN.
Gao Zi ZhanSchool of Acupuncture and Moxibustion and Massage, Anhui University of Chinese Medicine, Hefei, CHN.
Duan Wen XiuSchool of Acupuncture and Moxibustion and Massage, Anhui University of Chinese Medicine, Hefei, CHN.
Yu QingSchool of Acupuncture and Moxibustion and Massage, Anhui University of Chinese Medicine, Hefei, CHN.
Wang JieAcupuncture and Moxibustion Meridian Research Institute, Anhui Academy of Chinese Medicine, Hefei, CHN.
Cai Rong LinSchool of Acupuncture and Moxibustion and Massage, Anhui University of Chinese Medicine, Hefei, CHN.
Wu Zi JianSchool of Acupuncture and Moxibustion and Massage, Anhui University of Chinese Medicine, Hefei, CHN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveKnee osteoarthritis (KOA) is a chronic joint condition characterized by progressive cartilage degeneration and bone remodeling. Conventional drug treatments often provide limited relief and may cause adverse effects. As a nonpharmacological therapy in traditional Chinese medicine, moxibustion has been demonstrated to alleviate KOA-related pain, reduce inflammation, and ameliorate cartilage damage through immunomodulatory and metabolic pathways. This study aimed to explore the involvement of amino acid metabolism in the mechanism of the protective effects of moxibustion on cartilage injury in a rat model of KOA.

methodsSprague-Dawley rats were randomly assigned to three groups: normal, KOA model, and moxibustion treatment. The KOA model was established by intra-articular injection of 0.05 mL of a 30 mg/mL sodium iodoacetate solution into the right knee joint cavity of model and moxibustion groups. The moxibustion group received mild moxibustion treatment at Stomach Meridian 36 (ST36) on the right hind limb for 30 min daily over 30 consecutive days. The mechanical pain threshold was measured using Von Frey filaments, while joint swelling was assessed with an electronic caliper. Hematoxylin and eosin staining was performed to evaluate cartilage morphology, and a transmission electron microscope was used to observe chondrocyte ultrastructure. Levels of matrix metalloproteinase-13 (MMP-13) and interleukin-1β (IL-1β) in synovial tissue were quantified using enzyme-linked immunosorbent assay. Alterations in cartilage amino acid metabolites were analyzed using liquid chromatography-mass spectrometry.

resultsIn the normal group, the cartilage exhibited a smooth surface, with an intact matrix structure, and normal chondrocyte morphology. In contrast, the KOA model group presented with cartilage surface roughness, inflammatory cell infiltration, fibrosis, reduced chondrocyte density, nuclear pyknosis, and organelle damage after 30 days of chemical induction. Moxibustion alleviated structural damage, preserving hyaline cartilage, reducing inflammation and fibrosis, and improving chondrocyte morphology. Model rats displayed significant knee swelling (

conclusionMoxibustion at ST36 can significantly improve joint swelling, pain, synovitis, and chondrocyte injury in rats with KOA. It modulates immune response and cartilage synthesis and degradation through alanine, aspartate, and glutamate metabolic pathways, thereby exerting anti-inflammatory, analgesic, and protective effects on cartilage injury.

Indexed as

amino acid metabolismcartilage injurychinese medicineknee osteoarthritismoxibustion

Identifiers

PMID41446485
PMCPMC12723173

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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.