Abstract | ETHNOPHARMACOLOGICAL RELEVANCE: AIM OF THE STUDY: This study aimed to investigate the mechanisms by which MHCD treatment alleviates renal fibrosis. MATERIALS AND METHODS: An IgA nephropathy rat model was established using bovine serum albumin, carbon tetrachloride, and lipopolysaccharide. The rats were divided into control, model, telmisartan, low-dose MHCD, medium-dose MHCD, and high-dose MHCD groups. Treatments were administered to these groups for 8 weeks. Subsequently, the 24-h urine protein, serum creatinine, blood urea nitrogen, and blood albumin levels were measured. Pathological changes and degree of fibrosis in renal tissues were observed, and levels of the transforming growth factor-β1 (TGF-β1)/Smad3 signaling pathway components in renal tissues and TGF-β1 in urinary exosomes were measured. RESULTS:
Telmisartan and MHCD reduced 24-h urine protein levels, alleviated renal pathological injury, and decreased the renal expression of fibronectin, laminin, and collagen IV in rats with IgA nephropathy. Urinary exosomes were extracted and identified for further investigation of their role in renal fibrosis. MHCD reduced TGF-β1 expression in urinary exosomes and reduced TGF-β1 and p-Smad3 levels in renal tissues. CONCLUSION: MHCD alleviated renal fibrosis in rats with IgA nephropathy by inhibiting the TGF-β1/Smad3 signaling pathway through the downregulation of TGF-β1 expression in exosomes.
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Authors | Mingming Zhao, Bin Yang, Liusheng Li, Yuan Si, Meiying Chang, Sijia Ma, Ronghai Li, Yuejun Wang, Yu Zhang |
Journal | Journal of ethnopharmacology
(J Ethnopharmacol)
Vol. 285
Pg. 114795
(Mar 01 2022)
ISSN: 1872-7573 [Electronic] Ireland |
PMID | 34737009
(Publication Type: Journal Article)
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Copyright | Copyright © 2021 Elsevier B.V. All rights reserved. |
Chemical References |
- Antineoplastic Agents
- Drugs, Chinese Herbal
- Smad3 Protein
- Smad3 protein, rat
- Tgfb1 protein, rat
- Transforming Growth Factor beta1
- huangqi decoction
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Topics |
- Animals
- Antineoplastic Agents
(pharmacology)
- Disease Models, Animal
- Drugs, Chinese Herbal
(pharmacology)
- Exosomes
(metabolism)
- Fibrosis
- Gene Expression Regulation
(drug effects)
- Glomerulonephritis, IGA
(drug therapy, metabolism, pathology)
- Kidney
(drug effects, pathology)
- Rats
- Signal Transduction
(drug effects)
- Smad3 Protein
(metabolism)
- Transforming Growth Factor beta1
(metabolism)
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