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Sökning: id:"swepub:oai:lup.lub.lu.se:1d3e0dd0-13be-4c82-a262-d2c9c4b0ccb7" > Remote ischemic per...

Remote ischemic perconditioning attenuates adverse cardiac remodeling and preserves left ventricular function in a rat model of reperfused myocardial infarction

Pilz, Patrick M. (författare)
Medical University of Vienna
Hamza, Ouafa (författare)
Medical University of Vienna
Gidlöf, Olof (författare)
Lund University,Lunds universitet,Cardiovascular Epigenetics,Forskargrupper vid Lunds universitet,Lund University Research Groups
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Gonçalves, Ines F. (författare)
Medical University of Vienna
Tretter, Eva Verena (författare)
Medical University of Vienna
Trojanek, Sandra (författare)
Medical University of Vienna
Abraham, Dietmar (författare)
Medical University of Vienna
Heber, Stefan (författare)
Medical University of Vienna
Haller, Paul M. (författare)
Medical University of Vienna
Podesser, Bruno K. (författare)
Medical University of Vienna
Kiss, Attila (författare)
Medical University of Vienna
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 (creator_code:org_t)
Elsevier BV, 2019
2019
Engelska.
Ingår i: International Journal of Cardiology. - : Elsevier BV. - 0167-5273. ; 285, s. 72-79
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Aims: Remote ischemic conditioning (RIC) is considered a potential clinical approach to reduce myocardial infarct size and ameliorate adverse post-infarct left ventricular (LV) remodeling, however the mechanisms are unknown. The aim was to clarify the impact of RIC on Neuregulin-1 (NRG-1)/ErbBs expression, inflammation and LV hemodynamic function. Methods and results: Male Sprague-Dawley rats were subjected to 30 min occlusion of the left coronary artery (LCA) followed by 2 weeks of reperfusion and separated into three groups: (1) sham operated (without LCA occlusion); (2) Myocardial ischemia/reperfusion (MIR) and (3) remote ischemic perconditioning group (MIR + RIPerc). Cardiac structural and functional changes were evaluated by echocardiography and on the isolated working heart system. The level of H3K4me3 at the NRG-1 promoter, and both plasma and LV tissue levels of NRG-1 were assessed. The expression of pro-inflammatory cytokines, ECM components and ErbB receptors were assessed by RT-qPCR. MIR resulted in a significant decrease in LV function and enlargement of LV chamber. This was accompanied with a decrease in the level of H3K4me3 at the NRG-1 promoter. Consequently NRG-1 protein levels were reduced in the infarcted myocardium. Subsequently, an upregulated influx of CD68+ macrophages, high expression of MMP-2 and -9 as well as an increase of IL-1β TLR-4, TNF-α TNC expression were observed. In contrast, RIPerc significantly decreased inflammation and improved LV function in association with the enhancement of NRG-1 levels and ErbB3 expression. Conclusions: These findings may reveal a novel anti-remodeling and anti-inflammatory effect of RIPerc, involving activation of NRG-1/ErbB3 signaling.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Epigenetic
ErbB receptors
Inflammation
Myocardial infarction
Neuregulin-1
Remote ischemic perconditioning

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