Nelson 2015 Master Thesis: Difference between revisions

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{{Labeling
{{Labeling
|area=Respiration, Pharmacology;toxicology
|area=Respiration, Pharmacology;toxicology
|diseases=Cardiovascular, Diabetes
|organism=Mouse, Rat
|organism=Mouse, Rat
|tissues=Heart
|tissues=Heart, Other cell lines
|model cell lines=Other cell lines
|preparations=Permeabilized cells, Permeabilized tissue
|preparations=Permeabilized cells, Permeabilized tissue
|diseases=Cardiovascular, Diabetes
|couplingstates=LEAK, OXPHOS, ET
|couplingstates=LEAK, OXPHOS, ETS
|pathways=N, S, NS
|pathways=N, S, NS
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
}}
}}

Latest revision as of 15:29, 13 November 2017

Publications in the MiPMap
Nelson MB (2015) The role of receptors for advanced glycation end-products (RAGE) and ceramide in cardiovascular disease. Master Thesis 1-53.

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Nelson MB (2015) Master Thesis

Abstract: Type 2 diabetes and cigarette smoke exposure are associated with an increased risk of cardiovascular complications. The role of advanced glycation end-products (AGEs) is already well-established in numerous comorbidities including cardiomyopathy. Given the role of AGEs and their receptor, RAGE, in activating inflammatory pathways, we sought to determine whether ceramides could be a mediator of RAGE-induced altered heart mitochondrial function. Using an in vitro model, we treated H9C2 cardiomyocytes with carboxy-methyl lysine-BSA, followed by mitochondrial respiration assessment. We found that mitochondrial respiration was significantly impaired in AGE-treated cells, but not when co-treated with myriocin, an inhibitor of de novo ceramide biosynthesis. Moreover, we exposed WT and RAGE KO mice to side-stream cigarette smoke and found reduced mitochondrial respiration in the left ventricle myocardium from WT mice, but the RAGE KO mice were protected from this effect. Finally, conditional over-expression of RAGE in the lungs of mice also elicited a robust increase in left ventricular ceramides. Altogether, these findings suggest a RAGE-ceramide axis as an important contributor to cardiomyopathy. โ€ข Keywords: Rat H9C2 cardiomyocyte


Labels: MiParea: Respiration, Pharmacology;toxicology  Pathology: Cardiovascular, Diabetes 

Organism: Mouse, Rat  Tissue;cell: Heart, Other cell lines  Preparation: Permeabilized cells, Permeabilized tissue 


Coupling state: LEAK, OXPHOS, ET  Pathway: N, S, NS  HRR: Oxygraph-2k 


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