Chronic circadian disruption alters cardiac function and glucose regulation in mice

Data files for our manuscript :Gearey, Wang, Antle "Chronic circadian disruption alters cardiac function and glucose regulation in mice"

Cardiometabolic disease is a leading cause of death worldwide. One factor that may contribute to the risk, onset, and severity of symptoms is disrupted circadian rhythms. Our study uses two strains of mice to further elucidate this relationship: healthy controls, and a mouse model of insulin resistance with short freerunning periods (~22.75hrs) and enlarged hearts, raised in either a 24-hour or 22.75-hour LD cycle. Through glucose and insulin tolerance tests, routine electrocardiograms from 1-4 months old, and histology, we reveal worse cardiometabolic health outcomes for mice gestated and housed in a mismatched LD cycle compared to those in an LD cycle that matches their endogenous rhythm. This was characterized by heightened blood glucose levels following a glucose or insulin bolus, altered electrophysiological parameters of the cardiac waveform, and increased cardiomyocyte size. Circadian disruption due to work/social schedules or circadian-related disorders in people is often confounded with other unhealthy lifestyles. The present study demonstrates that circadian disruption on its own can lead to adverse health states.

The data sets included here look at:
1. Mouse ECG measured at 1, 2, and 4 months of age
2. Blood glucose levels following a challenge with Insulin (0.75IU/kg IP) at 3 months of age
3. Blood glucose levels following a challenge with glucose (2g/kg IP) at 3 months of age
4. body weight
5. Heart anatomy at 6 months of age.