Abstract
Background
Gastrointestinal (GI) symptoms in heart failure (HF) patients are associated with increased morbidity and mortality. We hypothesized that HF reduces bioelectrical activity underlying peristalsis. In this study, we aimed to establish a method to capture and analyze slow waves (SW) in the small intestine in mice with HF.
Methods
We established a model of HF secondary to coronary artery disease in mice overexpressing tissue‐nonspecific alkaline phosphatase (TNAP) in endothelial cells. The myoelectric activity was recorded from the small intestine in live animals under anesthesia. The low‐ and high‐frequency components of SW were isolated in MATLAB and compared between the control (n = 12) and eTNAP groups (n = 8). C‐kit‐positive interstitial cells of Cajal (ICC) and Pgp9.5‐positive myenteric neurons were detected by immunofluorescence. Myenteric ganglia were assessed by hematoxylin and eosin (H&E) staining.
Results
SW activity was successfully captured in vivo, with both high‐ and low‐frequency components. Low‐frequency component of SW was not different between endothelial TNAP (eTNAP) and control mice (mean[95% CI]: 0.032[0.025–0.039] vs. 0.040[0.028–0.052]). High‐frequency component of SW showed a reduction eTNAP mice relative to controls (0.221[0.140–0.302] vs. 0.394[0.295–0.489], p < 0.01). Dysrhythmia was also apparent upon visual review of signals. The density of ICC and neuronal networks remained the same between the two groups. No significant reduction in the size of myenteric ganglia of eTNAP mice was observed.
Conclusions
A method to acquire SW activity from small intestines in vivo and isolate low‐ and high‐frequency components was established. The results indicate that HF might be associated with reduced high‐frequency SW activity.
A method to acquire SW activity from small intestines in vivo and isolate low‐ and high‐frequency components was established. The results indicate that HF might be associated with reduced high‐frequency SW activity.