Effects of small platform catheter-based left ventricular assist device support on regional myocardial signal transduction Discussion

被引:3
|
作者
Slaughter, Mark
Dr Rajagopal
机构
[1] Division of Cardiac Surgery, Department of Surgery, University of Maryland School of Medicine and Medical Center, Baltimore, MD
来源
基金
美国国家卫生研究院;
关键词
intracellular signaling; left ventricular dysfunction; mechanical circulatory support; mechanotransduction; myocardial infarction;
D O I
10.1016/j.jtcvs.2015.08.035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Left ventricular (LV) assist device (LVAD) support reduces pathological loading. However, load-induced adaptive responses may be suppressed. Pathological loading dysregulates cardiac G protein-coupled receptor (GPCR) signaling. Signaling through G proteins is deleterious, whereas beta (beta)-arrestin-mediated signaling is cardioprotective. We examined the effects of pathological LV loading/LV dysfunction and treatment via LVAD, on beta-arrestin-mediated signaling, and genetic networks downstream of load. Methods: An ovine myocardial infarction (MI) model was used. Sheep underwent sham thoracotomy (n = 3), mid-left anterior descending coronary artery ligation to produce MI (n = 3), or MI with placement of a small-platform catheter-based LVAD (n = 3). LVAD support was continued for 2 weeks. Animals were maintained for a total of 12 weeks. Myocardial specimens were harvested and analyzed. Results: MI induced beta-arrestin activation. Increased interactions between epidermal growth factor receptor and beta-arrestins were observed. LVAD support inhibited these responses to MI (P < .05). LVAD support inhibited the activation of cardioprotective signaling effectors Akt (P < .05), and, to a lesser extent, extracellular regulated kinase 1/2 (P not significant); however, MI resulted in regional activation of load-induced GPCR signaling via G proteins, as assessed by the induction of atrial natriuretic peptide mRNA expression in the MI-adjacent zone relative to the MI-remote zone (P < .05). MI-adjacent zone atrial natriuretic peptide expression was renormalized with LVAD support. Conclusions: LVAD support inhibited cardioprotective beta-arrestin-mediated signaling. However, net benefits of normalization of load-induced GPCR signaling were observed in the MI-adjacent zone. These findings may have implications for the optimal extent and duration of unloading, and for the development of adjunctive medical therapies.
引用
收藏
页码:1341 / 1341
页数:1
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