Key result
Sleep deprivation lowers baseline LVDP by ~19% and worsens myocardial ischemia-reperfusion injury in rats.
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BACKGROUND: Sleep deprivation (SD) is strongly associated with elevated risk for cardiovascular disease. OBJECTIVE: To determine the effect of SD on basal hemodynamic functions and tolerance to myocardial ischemia-reperfusion (IR) injury in male rats. METHOD: SD was induced by using the flowerpot method for 4 days. Isolated hearts were perfused with Langendorff setup, and the following parameters were measured at baseline and after IR: left ventricular developed pressure (LVDP); heart rate (HR); and the maximum rate of increase and decrease of left ventricular pressure (± dp/dt). Heart NOx level, infarct size and coronary flow CK-MB and LDH were measured after IR. Systolic blood pressure (SBP) was measured at start and end of study. RESULTS: In the SD group, the baseline levels of LVDP (19%), +dp/dt (18%), and -dp/dt (21%) were significantly (p < 0.05) lower, and HR (32%) was significantly higher compared to the controls. After ischemia, hearts from SD group displayed a significant increase in HR together with a low hemodynamic function recovery compared to the controls. In the SD group, NOx level in heart, coronary flow CK-MB and LDH and infarct size significantly increased after IR; also SD rats had higher SBP after 4 days. CONCLUSION: Hearts from SD rats had lower basal cardiac function and less tolerance to IR injury, which may be linked to an increase in NO production following IR.
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Jeddi et al. (2015) studied Sleep deprivation and myocardial ischemia-reperfusion injury. Sleep deprivation (flowerpot method) vs. Control was evaluated on Basal hemodynamic functions (LVDP, +dp/dt, -dp/dt, HR) and tolerance to myocardial ischemia-reperfusion injury (p=<0.05). Sleep deprivation for 4 days in male rats lowered baseline LVDP by 19% (p<0.05), increased HR by 32%, and increased infarct size after ischemia-reperfusion injury.
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