Melatonin multiple effects on brown adipose tissue molecular machinery.


Journal

Journal of pineal research
ISSN: 1600-079X
Titre abrégé: J Pineal Res
Pays: England
ID NLM: 8504412

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 15 08 2018
revised: 18 12 2018
accepted: 18 12 2018
pubmed: 1 1 2019
medline: 24 5 2019
entrez: 1 1 2019
Statut: ppublish

Résumé

Brown adipose tissue (BAT) influences energy balance through nonshivering thermogenesis, and its metabolism daily and seasonal variations are regulated by melatonin through partially known mechanisms. We evaluated the role of melatonin in BAT molecular machinery of male Control, pinealectomized (PINX), and melatonin-treated pinealectomized (PINX/Mel) adult rats. BAT was collected either every 3 hours over 24 hours or after cold or high-fat diet (HFD) acute exposure. HFD PINX animals presented decreased Dio2 expression, while HFD PINX/Mel animals showed increased Dio2, Ucp1, and Cidea expression. Cold-exposed PINX rats showed decreased Dio2 and Lhs expression, and melatonin treatment augmented Adrβ3, Dio2, Ucp1, and Cidea expression. Daily profiles analyses showed altered Dio2, Lhs, Ucp1, Pgc1α, and Cidea gene and UCP1 protein expression in PINX animals, leading to altered rhythmicity under sub-thermoneutral conditions, which was partially restored by melatonin treatment. The same was observed for mitochondrial complexes I, II, and IV protein expression and enzyme activity. Melatonin absence seems to impair BAT responses to metabolic challenges, and melatonin replacement reverses this effect, with additional increase in the expression of crucial genes, suggesting that melatonin plays an important role in several key points of the thermogenic activation pathway, influencing both the rhythmic profile of the tissue and its ability to respond to metabolic challenges, which is crucial for the organism homeostasis.

Identifiants

pubmed: 30597601
doi: 10.1111/jpi.12549
doi:

Substances chimiques

Melatonin JL5DK93RCL

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e12549

Subventions

Organisme : Fundação de Amparo à Pesquisa do Estado de São Paulo
ID : 2014/50457-0
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 133425/2016-9
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 446888/2014-1

Informations de copyright

© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Auteurs

Caroline A P de Souza (CAP)

Pineal Neurobiology Lab, Department of Physiology, Federal University of São Paulo, São Paulo, Brazil.

Camila Congentino Gallo (CC)

Pineal Neurobiology Lab, Department of Physiology, Federal University of São Paulo, São Paulo, Brazil.

Ludmilla Scodeler de Camargo (LS)

Pineal Neurobiology Lab, Department of Physiology, Federal University of São Paulo, São Paulo, Brazil.

Paula Vargas Versignassi de Carvalho (PVV)

Pineal Neurobiology Lab, Department of Physiology, Federal University of São Paulo, São Paulo, Brazil.

Ingrid Fernandes Olesçuck (IF)

Pineal Neurobiology Lab, Department of Physiology, Federal University of São Paulo, São Paulo, Brazil.

Felipe Macedo (F)

Department of Biochemistry, Federal University of São Paulo, São Paulo, Brazil.

Fernanda Marques da Cunha (FM)

Department of Biochemistry, Federal University of São Paulo, São Paulo, Brazil.

José Cipolla-Neto (J)

Laboratory of Neurobiology, Department of Physiology and Biophysics, University of São Paulo, São Paulo, Brazil.

Fernanda G do Amaral (FG)

Pineal Neurobiology Lab, Department of Physiology, Federal University of São Paulo, São Paulo, Brazil.

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Classifications MeSH