Repository of Research and Investigative Information

Repository of Research and Investigative Information

Shahid Sadoughi University of Medical Sciences

Antioxidant therapy against TGF-β/SMAD pathway involved in organ fibrosis

(2024) Antioxidant therapy against TGF-β/SMAD pathway involved in organ fibrosis. Journal of Cellular and Molecular Medicine. ISSN 15821838 (ISSN)

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Official URL: https://www.scopus.com/inward/record.uri?eid=2-s2....

Abstract

Fibrosis refers to excessive build-up of scar tissue and extracellular matrix components in different organs. In recent years, it has been revealed that different cytokines and chemokines, especially Transforming growth factor beta (TGF-β) is involved in the pathogenesis of fibrosis. It has been shown that TGF-β is upregulated in fibrotic tissues, and contributes to fibrosis by mediating pathways that are related to matrix preservation and fibroblasts differentiation. There is no doubt that antioxidants protect against different inflammatory conditions by reversing the effects of nitrogen, oxygen and sulfur-based reactive elements. Oxidative stress has a direct impact on chronic inflammation, and as results, prolonged inflammation ultimately results in fibrosis. Different types of antioxidants, in the forms of vitamins, natural compounds or synthetic ones, have been proven to be beneficial in the protection against fibrotic conditions both in vitro and in vivo. In this study, we reviewed the role of different compounds with antioxidant activity in induction or inhibition of TGF-β/SMAD signalling pathway, with regard to different fibrotic conditions such as gastro-intestinal fibrosis, cardiac fibrosis, pulmonary fibrosis, skin fibrosis, renal fibrosis and also some rare cases of fibrosis, both in animal models and cell lines. © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.

Item Type: Article
Keywords: antioxidants extracellular matrix organ fibrosis oxidative stress TGF-β/SMAD pathway Animals Fibrosis Inflammation Pulmonary Fibrosis Smad Proteins Transforming Growth Factor beta Transforming Growth Factor beta1 acetylcysteine alkaloid alpha smooth muscle actin alpha tocopherol antioxidant baicalin catalase chemokine curcumin edaravone flavonoid glutathione heme oxygenase 1 inducible nitric oxide synthase losartan magnolol melatonin nitrogen ovalbumin oxygen peroxisome proliferator activated receptor gamma polyphenol prion protein reactive oxygen metabolite sodium glucose cotransporter 2 inhibitor streptozocin superoxide dismutase testosterone titanium dioxide titanium dioxide nanoparticle transcription factor Nrf2 vimentin vitamin D Smad protein angiogenesis antihypertensive activity antioxidant therapy anxiety apoptosis Bagg albino mouse C57BL 6 mouse cell differentiation chronic inflammation Crohn disease diabetic cardiomyopathy down regulation drug combination drug mechanism Duchenne muscular dystrophy endoplasmic reticulum stress epithelial mesenchymal transition fibroblast fibrosing alveolitis gene expression glomerulosclerosis heart failure heart infarction heart muscle fibrosis hemodialysis in vitro study inflammatory bowel disease intestinal fibrosis kidney fibrosis Leporidae lipid diet liver cirrhosis liver fibrosis lung fibrosis medical procedures molecular docking myofibroblast nonhuman pathogenesis physiological stress protein aggregation retina detachment Review risk factor scar tissue signal transduction skin fibrosis Smad signaling spine surgery TGF beta SMAD signaling pathway traditional medicine ulcerative colitis vitreoretinopathy Wistar rat animal metabolism
Journal or Publication Title: Journal of Cellular and Molecular Medicine
Journal Index: Scopus
Volume: 28
Number: 2
Identification Number: https://doi.org/10.1111/jcmm.18052
ISSN: 15821838 (ISSN)
Depositing User: ms soheila Bazm
URI: http://eprints.ssu.ac.ir/id/eprint/34321

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