Annually 785,000 people in the United States suffer from myocardial infarction (MI). MI often results in decreased contractility, electrical instabilit, and tissue necrosis in the heart leading to lethal cardiac arrhythmias and 22% of men and 46% of women are diagnosed with heart failure (HF) within six years. Stem cell therapy has gained relevance as a technique to repair the damaged myocardium. However, while this treatment shows great promise, there are limitations. One such limitation is after transplantation, only a very low percentage of the injected cells remain in the injured myocardium, known as low cell engraftment rate. This critical issue needs to be addressed before stem cell therapies can be applied in clinical settings.
This research aims at addressing this limitation and improving cardiac stem cell therapies for the treatment of MI and MI-induced HF. Vagal nerve stimulation (VNS) is a contemporaneous emerging potential therapy for the treatment of injured hearts. VNS has been shown to 1) greatly reduce inflammation and 2) markedly suppress arrhythmias in animals with MI. Our major hypothesis is that the anti-inflammatory mechanism of VNS will result in an increase in stem cell engraftment while the anti-arrhythmic effects of VNS will reduce the likelihood of arrhythmias associated with MI injury and/or stem cell transplantation. We propose to implement three specific aims in order to test our hypothesis. First, we aim to determine the optimal time for the onset of VNS to obtain maximal anti- inflammatory effects. Specifically, we will investigate four different timings of VNS, i.e. 1) 30 minutes prior to ischema, 2) at the onset of ischemia, 3) 15 minutes at ischemia, or 4) at the onset of reperfusion, and precisely determine which will provide the optimal benefits. After determining this optimal time, we will use this time to complete our remaining two aims. Second, we aim to study the long term anti-inflammatory effects of VNS and stem cell engraftment rate to test our hypothesis that VNS therapy is able to create an intramyocardial microenvironment more receptive to stem cell transplantation and differentiation due to its anti-inflammatory effects, and thus, increase engraftment rate. Third, we aim to perform telemetric ECG and blood pressure measurements, echocardiography, in vivo ventricular fibrillation induction, and optical mapping experiments to assess the electrophysiological and functional effects of the combined VNS and stem cell therapy to test our hypothesis that stem cell transplantation in combination with active VNS will result in higher levels of stem cell engraftment, and thus, an enhanced healing of the damaged heart. We anticipate that the outcome of this work will be pivotal in the development of a novel combination therapy to treat MI patients.

Public Health Relevance

Stem cell therapies have not been successful in treating myocardial infarction (or heart attacks) due to poor stem cell survival and the risk of generating abnormal electrical rhythms in the heart upon stem cell transplantation. The long-term goal of the proposed work is to address these limitations by incorporating vagal nerve stimulation with stem cell therapy in a myocardial infarction rat model. This multifaceted approach could lead to greater improvements in the injured heart and have the potential to substantially contribute to the translation of cardiac stem cell therapies into clinical practice, and thus, benefit patients directly.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31HL129544-02
Application #
9119529
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Cooper, Lawton S
Project Start
2015-07-01
Project End
2018-09-11
Budget Start
2016-09-12
Budget End
2017-09-11
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Biomedical Engineering
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Lee, Steven W; Anderson, Allison; Guzman, Pilar A et al. (2018) Atrial GIRK Channels Mediate the Effects of Vagus Nerve Stimulation on Heart Rate Dynamics and Arrhythmogenesis. Front Physiol 9:943
Kulkarni, Kanchan; Lee, Steven W; Kluck, Ryan et al. (2018) Real-Time Closed Loop Diastolic Interval Control Prevents Cardiac Alternans in Isolated Whole Rabbit Hearts. Ann Biomed Eng 46:555-566
Lee, Steven W; Li, Qinglu; Libbus, Imad et al. (2016) Chronic cyclic vagus nerve stimulation has beneficial electrophysiological effects on healthy hearts in the absence of autonomic imbalance. Physiol Rep 4:
Kulkarni, Kanchan; Lee, Steven W; Tolkacheva, Elena G (2016) Pro-arrhythmic effect of heart rate variability during periodic pacing. Conf Proc IEEE Eng Med Biol Soc 2016:149-152