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Targeting vascular smooth muscle cell dysfunction with xanthine derivative KMUP-3 inhibits abdominal aortic aneurysm in mice.
- Source :
-
Atherosclerosis [Atherosclerosis] 2020 Mar; Vol. 297, pp. 16-24. Date of Electronic Publication: 2020 Feb 06. - Publication Year :
- 2020
-
Abstract
- Background and Aims: Inflammation, oxidative stress, matrix degradation, medial calcification and vascular smooth muscle cell (VSMC) loss are prominent features in abdominal aortic aneurysm (AAA). VSMC phenotypic switch to a proinflammatory state and VSMC apoptosis could be targetable mechanisms implicated in the pathogenesis of AAA formation. Herein, we investigated the hypothesis that a xanthine derivative (KMUP-3) might suppress AAA through inhibition of VSMC phenotypic switch and apoptosis.<br />Methods: In vitro, VSMC calcification was induced using β-glycerophosphate. In vivo, AAA was induced using angiotensin II (1000 ng/kg per minute) infusion for 4 weeks in apolipoprotein E-deficient mice.<br />Results: As determined by alizarin red S staining and calcium content measurements, KMUP-3 suppressed VSMC calcification. During VSMC calcification, KMUP-3 inhibited mTOR and β-catenin upregulation, essential for VSMC phenotypic switch, while it enhanced AMP-activated protein kinase (AMPK) activation that protects against VSMC phenotypic switch. Moreover, KMUP-3 attenuated VSMC apoptosis with an increased Bcl-2/Bax ratio and reduced activated caspase-3 expression. During AAA formation, treatment with KMUP-3 inhibited phosphorylated mTOR expression and increased phosphorylated AMPK expression in the medial layer. In addition, KMUP-3 treatment suppressed aortic dilatation together with reduction in proinflammatory cytokines and infiltrating macrophages, attenuation of medial VSMC apoptosis and mitigation of reactive oxygen species generation, matrix-degrading proteinase activities, elastin breakdown and vascular calcification.<br />Conclusions: Treatment with KMUP-3 inhibits aneurysm growth possibly through its interference with signaling pathways involved in VSMC phenotypic switch and apoptosis. These findings provide a proof-of-concept validation for VSMC dysfunction as a potential therapeutic target in AAA.<br />Competing Interests: Declaration of competing interest The authors declared they do not have anything to disclose regarding conflict of interest with respect to this manuscript.<br /> (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Subjects :
- Angiotensin II
Animals
Aorta, Abdominal drug effects
Aorta, Abdominal metabolism
Aorta, Abdominal pathology
Aortic Aneurysm, Abdominal chemically induced
Aortic Aneurysm, Abdominal metabolism
Aortic Aneurysm, Abdominal pathology
Apoptosis Regulatory Proteins metabolism
Cells, Cultured
Disease Models, Animal
Male
Mice, Knockout, ApoE
Muscle, Smooth, Vascular metabolism
Muscle, Smooth, Vascular pathology
Myocytes, Smooth Muscle metabolism
Myocytes, Smooth Muscle pathology
Phenotype
Rats, Sprague-Dawley
Signal Transduction
Vascular Calcification metabolism
Vascular Calcification pathology
Aortic Aneurysm, Abdominal prevention & control
Apoptosis drug effects
Muscle, Smooth, Vascular drug effects
Myocytes, Smooth Muscle drug effects
Piperidines pharmacology
Vascular Calcification prevention & control
Xanthines pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-1484
- Volume :
- 297
- Database :
- MEDLINE
- Journal :
- Atherosclerosis
- Publication Type :
- Academic Journal
- Accession number :
- 32059119
- Full Text :
- https://doi.org/10.1016/j.atherosclerosis.2020.01.029