Abstract | BACKGROUND AND PURPOSE: METHODS: We established an arthritis model by combining chicken type II collagen and complete Freund's adjuvant. Resveratrol treatment was administered via tube feeding for 10 days. Pathological changes in both the joints and lungs were evaluated using HE and Masson staining techniques. Protein expression of TGF-β1, AKT, and TMEM175 was examined in lung tissue. MRC-5 cells were stimulated using IL-1β in combination with TGF-β1 as an in vitro model of RA-ILD, and agonists of AKT, metabolic inhibitors, and SiRNA of TMEM175 were used to explore the regulation and mechanism of action of resveratrol RA-ILD. RESULTS:
Resveratrol mitigates fibrosis in rheumatoid arthritis-associated interstitial lung disease and reduces oxidative stress and inflammation in RA-ILD. Furthermore, resveratrol restored cellular autophagy. When combined with the in vitro model, it was further demonstrated that resveratrol could suppress TGF-β1 expression, and reduce AKT metamorphic activation, consequently inhibiting the opening of AKT/MEM175 ion channels. This, in turn, lowers lysosomal pH and enhances the fusion of autophagosomes with lysosomes, ultimately ameliorating the progression of RA-ILD. CONCLUSION: In this study, we demonstrated that resveratrol restores autophagic flux through the AKT/MEM175 pathway to attenuate inflammation as well as fibrosis in RA-ILD by combining in vivo and in vitro experiments. It further provides a theoretical basis for the selection of therapeutic targets for RA-ILD.
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Authors | Nannan Liu, Xuefei Fan, Yubao Shao, Suhuan Chen, Taorong Wang, Tao Yao, Xiaoyu Chen |
Journal | Journal of translational medicine
(J Transl Med)
Vol. 22
Issue 1
Pg. 457
(May 14 2024)
ISSN: 1479-5876 [Electronic] England |
PMID | 38745204
(Publication Type: Journal Article)
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Copyright | © 2024. The Author(s). |
Topics |
- Resveratrol
(pharmacology, therapeutic use)
- Arthritis, Rheumatoid
(complications, drug therapy, pathology)
- Proto-Oncogene Proteins c-akt
(metabolism)
- Animals
- Lung Diseases, Interstitial
(drug therapy, complications, pathology, metabolism)
- Humans
- Inflammation
(pathology, drug therapy)
- Signal Transduction
(drug effects)
- Fibrosis
- Transforming Growth Factor beta1
(metabolism)
- Membrane Proteins
(metabolism)
- Autophagy
(drug effects)
- Oxidative Stress
(drug effects)
- Cell Line
- Lung
(pathology, drug effects)
- Male
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