Consequences of low-intensity light at night on cardiovascular and metabolic parameters in spontaneously hypertensive rats 1

• Published in: Canadian journal of physiology and pharmacology 2019-09, Vol.97 (9), p.863-871
• Main Authors: Rumanova, Valentina Sophia, Okuliarova, Monika, Molcan, Lubos, Sutovska, Hana, Zeman, Michal
• Format: Article
• Language: English
• Subjects: Animals; Blood Pressure - physiology; Blood Pressure - radiation effects; Circadian Rhythm - physiology; Circadian Rhythm - radiation effects; Dose-Response Relationship, Radiation; Heart Rate - physiology; Heart Rate - radiation effects; Insulin - blood; Insulin Resistance - physiology; Insulin Resistance - radiation effects; Leptin - blood; Light - adverse effects; Male; Rats; Rats, Inbred SHR
• ISSN: 1205-7541
• DOI: 10.1139/cjpp-2019-0043

Circadian rhythms are an inherent property of physiological processes and can be disturbed by irregular environmental cycles, including artificial light at night (ALAN). Circadian disruption may contribute to many pathologies, such as hypertension, obesity, and type 2 diabetes, but the underlying mechanisms are not understood. Our study investigated the consequences of ALAN on cardiovascular and metabolic parameters in spontaneously hypertensive rats, which represent an animal model of essential hypertension and insulin resistance. Adult males were exposed to a 12 h light - 12 h dark cycle and the ALAN group experienced dim light at night (1-2 lx), either for 2 or 5 weeks. Rats on ALAN showed a loss of light-dark variability for systolic blood pressure, but not for heart rate. Moreover, a gradual increase of systolic blood pressure was recorded over 5 weeks of ALAN. Exposure to ALAN increased plasma insulin and hepatic triglyceride levels. An increased expression of metabolic transcription factors, and , in the epididymal fat and a decreased expression of in the heart was found in the ALAN group. Our results demonstrate that low-intensity ALAN can disturb blood pressure control and augment insulin resistance in spontaneously hypertensive rats, and may represent a serious risk factor for cardiometabolic diseases.