Chronic treatment with dexamethasone alters clock gene expression and melatonin synthesis in rat pineal gland at night

• Published in: Nature and science of sleep 2018-01, Vol.10, p.203-215
• Main Authors: Meneses-Santos, Daniela, Buonfiglio, Daniella do Carmo, Peliciari-Garcia, Rodrigo Antonio, Ramos-Lobo, Angela Maria, Souza, Divanízia do Nascimento, Carpinelli, Angelo Rafael, Carvalho, Carla Roberta de Oliveira, Sertie, Rogério Antônio Laurato, Andreotti, Sandra, Lima, Fabio Bessa, Afeche, Solange Castro, Fioretto, Emerson Ticona, Cipolla-Neto, José, Marçal, Anderson Carlos
• Format: Article
• Language: English
• Subjects: Body weight; Circadian rhythm; Clock genes; Dexamethasone; EDTA; Endocrine system; Enzymes; Gene expression; Genes; Genetic aspects; Genomics; Glucocorticoids; Glucose; Homeostasis; Hormones; Hyperglycemia; Insulin; Kinases; Laboratory animals; Mammals; Melatonin; Nervous system; Original Research; Physiological aspects; Physiology; Pineal gland; Proteins; Steroids; Steroids (Organic compounds)
• ISSN: 1179-1608; 1179-1608
• DOI: 10.2147/NSS.S158602

Melatonin is a neuroendocrine hormone that regulates many functions involving energy metabolism and behavior in mammals throughout the light/dark cycle. It is considered an output signal of the central circadian clock, located in the suprachiasmatic nucleus of the hypothalamus. Melatonin synthesis can be influenced by other hormones, such as insulin and glucocorticoids in pathological conditions or during stress. Furthermore, glucocorticoids appear to modulate circadian clock genes in peripheral tissues and are associated with the onset of metabolic diseases. In the pineal gland, the modulation of melatonin synthesis by clock genes has already been demonstrated. However, few studies have shown the effects of glucocorticoids on clock genes expression in the pineal gland. We verified that rats treated with dexamethasone (2 mg/kg body weight, intraperitoneal) for 10 consecutive days, showed hyperglycemia and pronounced hyperinsulinemia during the dark phase. Insulin sensitivity, glucose tolerance, melatonin synthesis, and enzymatic activity of arylalkylamine -acetyltransferase, the key enzyme of melatonin synthesis, were reduced. Furthermore, we observed an increase in the expression of in pineal glands of rats treated with dexamethasone. These results show that chronic treatment with dexamethasone can modulate both melatonin synthesis and circadian clock expression during the dark phase.