Cargando…
Recurrent inhibition of mitochondrial complex III induces chronic pulmonary vasoconstriction and glycolytic switch in the rat lung
BACKGROUND: Pulmonary arterial hypertension (PAH) is a fatal disease; however, the mechanisms directly involved in triggering and the progression of PAH are not clear. Based on previous studies that demonstrated a possible role of mitochondrial dysfunction in the pathogenesis of PAH, we investigated...
Autores principales: | Rafikova, Olga, Srivastava, Anup, Desai, Ankit A., Rafikov, Ruslan, Tofovic, Stevan P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914012/ https://www.ncbi.nlm.nih.gov/pubmed/29685148 http://dx.doi.org/10.1186/s12931-018-0776-1 |
Ejemplares similares
-
Complex III Inhibition-Induced Pulmonary Hypertension Affects the Mitochondrial Proteomic Landscape
por: James, Joel, et al.
Publicado: (2020) -
Complex I dysfunction underlies the glycolytic switch in pulmonary hypertensive smooth muscle cells
por: Rafikov, Ruslan, et al.
Publicado: (2015) -
Role of Gender in Regulation of Redox Homeostasis in Pulmonary Arterial Hypertension
por: Rafikov, Ruslan, et al.
Publicado: (2019) -
Focus on Early Events: Pathogenesis of Pulmonary Arterial Hypertension Development
por: Rafikova, Olga, et al.
Publicado: (2019) -
Pulmonary Arterial Hypertension Induces a Distinct Signature of Circulating Metabolites
por: Rafikov, Ruslan, et al.
Publicado: (2020)