Melatonin deficiency decreases brown adipose tissue acute thermogenic capacity of in rats measured by 18F-FDG PET

• Main Authors: Bruno Halpern, Marcio C. Mancini, Caroline Mendes, Camila Maria Longo Machado, Silvana Prando, Marcelo Tatit Sapienza, Carlos Alberto Buchpiguel, Fernanda Gaspar do Amaral, José Cipolla-Neto
• Format: Article
• Language: English
• Published: BMC 2020-09-01
• Series: Diabetology & Metabolic Syndrome
• Subjects: Brown adipose tissue; Melatonin; Obesity; Circadian rhythms; FDG-PET; Thermogenesis
• Online Access: http://link.springer.com/article/10.1186/s13098-020-00589-1

Abstract Objective Melatonin has been shown to increase brown adipose tissue (BAT) mass, which can lead to important metabolic effects, such as bodyweight reduction and glycemic improvement. However, BAT mass can only be measured invasively and. The gold standard for non-invasive measurement of BAT activity is positron emission tomography with 2-deoxy-2-[fluorine-18] fluoro-d-glucose (18F-FDG PET). There is no study, to our knowledge, that has evaluated if melatonin influences BAT activity, measured by this imaging technique in animals. Methods Three experimental groups of Wistar rats (control, pinealectomy, and pinealectomy replaced with melatonin) had an 18F-FDG PET performed at room temperature and after acute cold exposure. The ratio of increased BAT activity after cold exposure/room temperature was called “acute thermogenic capacity” (ATC) We also measured UCP-1 mRNA expression to correlate with the 18F-FDG PET results. Results Pinealectomy led to reduced acute thermogenic capacity, compared with the other groups, as well as reduced UCP1 mRNA expression. Conclusion Melatonin deficiency impairs BAT response when exposed to acute cold exposure. These results can lead to future studies of the influence of melatonin on BAT, in animals and humans, without needing an invasive evaluation of BAT.