| Literature DB >> 29736746 |
Genya Sunagawa1, Keita Saku2, Takahiro Arimura1, Takuya Nishikawa1, Hiroshi Mannoji1, Kazuhiro Kamada1, Kiyokazu Abe3, Takuya Kishi4, Hiroyuki Tsutsui1, Kenji Sunagawa5.
Abstract
The oxygen supply-demand imbalance is the fundamental pathophysiology of myocardial infarction (MI). Reducing myocardial oxygen consumption (MVO2) in acute MI (AMI) reduces infarct size. Since left ventricular (LV) mechanical work and heart rate are major determinants of MVO2, we hypothesized that the combination of LV mechanical unloading and chronotropic unloading during AMI can reduce infarct size via synergistic suppression of MVO2. In a dog model of ischemia-reperfusion, as we predicted, the combination of mechanical unloading by Impella and bradycardic agent, ivabradine (IVA), synergistically reduced MVO2. This was translated into the striking reduction of infarct size with Impella + IVA administered 60 min after the onset of ischemia compared to no treatment (control) and Impella groups (control 56.3 ± 6.5, Impella 39.9 ± 7.4 and Impella + IVA 23.7 ± 10.6%, p < 0.001). In conclusion, Impella + IVA during AMI reduced infarct size via marked suppression of MVO2. The mechano-chronotropic unloading may serve as a powerful therapeutic option for AMI.Entities:
Keywords: Acute myocardial infarction; Impella; Infarct size; Ivabradine; Left ventricular assist device; Pressure-volume loop
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Year: 2018 PMID: 29736746 DOI: 10.1007/s12265-018-9809-x
Source DB: PubMed Journal: J Cardiovasc Transl Res ISSN: 1937-5387 Impact factor: 4.132