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Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid

Oberbach, A; Jehmlich, N; Schlichting, N; Heinrich, M; Lehmann, S; Wirth, H; Till, H; Stolzenburg, JU; Völker, U; Adams, V; Neuhaus, J.
Molecular fingerprint of high fat diet induced urinary bladder metabolic dysfunction in a rat model.
PLoS One. 2013; 8(6):e66636-e66636 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Autor/innen der Med Uni Graz:
Till Holger
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Number of Figures: 6
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Abstract:
Diabetic voiding dysfunction has been reported in epidemiological dimension of individuals with diabetes mellitus. Animal models might provide new insights into the molecular mechanisms of this dysfunction to facilitate early diagnosis and to identify new drug targets for therapeutic interventions. Thirty male Sprague-Dawley rats received either chow or high-fat diet for eleven weeks. Proteomic alterations were comparatively monitored in both groups to discover a molecular fingerprinting of the urinary bladder remodelling/dysfunction. Results were validated by ELISA, Western blotting and immunohistology. In the proteome analysis 383 proteins were identified and canonical pathway analysis revealed a significant up-regulation of acute phase reaction, hypoxia, glycolysis, β-oxidation, and proteins related to mitochondrial dysfunction in high-fat diet rats. In contrast, calcium signalling, cytoskeletal proteins, calpain, 14-3-3η and eNOS signalling were down-regulated in this group. Interestingly, we found increased ubiquitin proteasome activity in the high-fat diet group that might explain the significant down-regulation of eNOS, 14-3-3η and calpain. Thus, high-fat diet is sufficient to induce significant remodelling of the urinary bladder and alterations of the molecular fingerprint. Our findings give new insights into obesity related bladder dysfunction and identified proteins that may indicate novel pathophysiological mechanisms and therefore constitute new drug targets.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Blotting, Western -
Cells, Cultured -
Chromatography, High Pressure Liquid -
Diet, High-Fat -
Disease Models, Animal -
Enzyme-Linked Immunosorbent Assay -
Male -
Phenotype -
Proteome -
Rats -
Rats, Sprague-Dawley -
Tandem Mass Spectrometry -
Urinary Bladder - metabolism
Urinary Bladder Diseases - etiology

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