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Salvanic acid B inhibits myocardial fibrosis through regulating TGF-β1/Smad signaling pathway
- Source :
- Biomedicine & Pharmacotherapy, Vol 110, Iss, Pp 685-691 (2019)
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- Objective: Salvanic Acid B (Sal B) was proved to show significant effect against fibrosis and myocardial injury. This study aimed to investigate the protective effects and the mechanisms of Sal B on myocardial fibrosis. Methods: The mice were randomly assigned to five groups: control group, model group, positive group, low-dose group, high-dose group. Hematoxylin-Eosin (HE) staining and Masson staining were used to assess the myocardial physiological changes and measure the myocardial fibrosis area. Expression of transforming growth factor-beta (TGF-β), drosophila mothers against decapentaplegic (Smad)2, Smad3 and Smad7 were analyzed by immunohistochemistry and real-time PCR. On the other hand, mouse cardiac fibroblasts (CFs) cells were co-treated with 20 ng/mL TGF-β1 and different concentrations of Sal B (5, 10, and 20 ng/mL) for 24 h. The cells morphology changes were assessed under a microscope, and the protein expressions induced by TGF-β1 were detected by Western blot. Results: Compared with the model group, myocardial collagen fibers decreased obviously with Sal B treatment (p
- Subjects :
- Male
0301 basic medicine
Myocardial Infarction
Salvia miltiorrhiza
RM1-950
SMAD
Transforming Growth Factor beta1
Mice
03 medical and health sciences
0302 clinical medicine
Western blot
Fibrosis
Myocardial fibrosis
medicine
Animals
Pharmacology
Dose-Response Relationship, Drug
Salvanic acid B
medicine.diagnostic_test
Plant Extracts
Signaling pathway
Chemistry
General Medicine
medicine.disease
Smad Proteins, Receptor-Regulated
Molecular biology
030104 developmental biology
030220 oncology & carcinogenesis
Immunohistochemistry
Therapeutics. Pharmacology
Mothers against decapentaplegic
Signal transduction
Signal Transduction
Transforming growth factor
Subjects
Details
- ISSN :
- 07533322
- Volume :
- 110
- Database :
- OpenAIRE
- Journal :
- Biomedicine & Pharmacotherapy
- Accession number :
- edsair.doi.dedup.....64b009dfde2b6becd4bf2f06f0e5169f