Uremia aggravates left ventricular remodeling after myocardial infarction

Background: Renal failure is a well-established cardiovascular risk factor. We hypothesized that uremia negatively affects post-myocardial infarction (MI) remodeling and left ventricular (LV) function and examined the pathohistological correlations. Methods: Subtotally nephrectomized rats (SNX) and...

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Main Authors: Dikow, Ralf (Author) , Schmidt, Ulrike Stefanie (Author) , Kihm, Lars Philipp (Author) , Schaier, Matthias (Author) , Schwenger, Vedat (Author) , Groß-Weissmann, Marie-Luise (Author) , Katus, Hugo (Author) , Zeier, Martin (Author) , Hardt, Stefan (Author)
Format: Article (Journal)
Language:English
Published: May 19, 2010
In: American journal of nephrology
Year: 2010, Volume: 32, Issue: 1, Pages: 13-22
ISSN:1421-9670
DOI:10.1159/000313846
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1159/000313846
Verlag, lizenzpflichtig, Volltext: https://www.karger.com/Article/FullText/313846
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Author Notes:Ralf Dikow, Ulrike Schmidt, Lars P. Kihm, Matthias Schaier, Vedat Schwenger, Marie-Luise Gross, Hugo A. Katus, Martin Zeier, Stefan E. Hardt
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Summary:Background: Renal failure is a well-established cardiovascular risk factor. We hypothesized that uremia negatively affects post-myocardial infarction (MI) remodeling and left ventricular (LV) function and examined the pathohistological correlations. Methods: Subtotally nephrectomized rats (SNX) and controls with MI only (MIC) were examined 1, 4 and 8 weeks after MI. MI size, ejection fraction (EF), cardiac fibrosis, vascular density and cardiomyocyte density were studied. Results: The extension of MI was 0.08 ± 0.02 in SNX versus 0.06 ± 0.02 in MIC rats (p < 0.031). Prior to MI, EF was comparable in SNX and MIC (74 ± 3 vs. 72 ± 2%, n.s.). Despite a relatively small infarct size EF in SNX decreased to 58 ± 4% 1 week after infarction and progressively worsened to 51 ± 4% after 8 weeks. In MIC animals EF only slightly decreased 1 week after MI (70 ± 3%) and remained unchanged at follow-up. In SNX animals LV end-diastolic diameter continuously increased following MI throughout the study period indicating accelerated remodeling. Furthermore, accelerated myocardial fibrosis was already notable 1 week after MI in SNX animals and the volume density of capillaries and cardiomyocytes was significantly lower in SNX rats. Conclusion: MI in experimental uremia is associated with progressive impairment of LV function, LV dilatation and accelerated myocardial fibrosis.
Item Description:Gesehen am 02.02.2023
Physical Description:Online Resource
ISSN:1421-9670
DOI:10.1159/000313846