Melatonin modulates swine luteal and adipose stromal cell functions.
Adipogenesis
/ drug effects
Adipose Tissue
/ cytology
Animals
Cell Proliferation
/ drug effects
Cells, Cultured
Corpus Luteum
/ cytology
Female
Leptin
/ metabolism
Melatonin
/ pharmacology
Nitric Oxide
/ metabolism
Oxidation-Reduction
PPAR gamma
/ metabolism
Progesterone
/ biosynthesis
Receptor, Melatonin, MT2
/ agonists
Stromal Cells
/ drug effects
Sus scrofa
Journal
Reproduction, fertility, and development
ISSN: 1031-3613
Titre abrégé: Reprod Fertil Dev
Pays: Australia
ID NLM: 8907465
Informations de publication
Date de publication:
Feb 2021
Feb 2021
Historique:
received:
01
12
2020
accepted:
08
12
2020
pubmed:
2
2
2021
medline:
5
11
2021
entrez:
1
2
2021
Statut:
ppublish
Résumé
Based on our previous study in follicles, the first aim of this work was to evaluate the effect of melatonin in the swine corpus luteum (CL). Luteal cells were exposed to 10 and 20pg mL-1 melatonin. We evaluated the effect on proliferation (bromo-deoxy-uridine uptake), steroidogenesis (progesterone) and redox status by means of Griess test (nitric oxide production), WST-1 test (superoxide anion generation) and FRAP test (non-enzymatic antioxidant power). The results showed a significant increase in antioxidant power, as well as a reduction in the other parameters analysed. These data and the expression of MT2 observed in luteal cells allow us to hypothesise a physiological role of melatonin in the regulation of CL functionality. The reproductive function is dependent on energy reserves stored in adipose tissue. Therefore, we sought to verify the effect of melatonin on adipose stromal cells (ASCs). MT2 receptor expression was detected in ASCs and the presence of gene markers (PPARγ and leptin) before and after adipogenic differentiation was verified. The differentiation was significantly inhibited by melatonin, as well as cell viability. In conclusion, present results suggest that melatonin exerts a potential inhibitory action on luteal function and adipogenesis, possibly mediated by MT2.
Identifiants
pubmed: 33524309
pii: RD20312
doi: 10.1071/RD20312
doi:
Substances chimiques
Leptin
0
PPAR gamma
0
Receptor, Melatonin, MT2
0
Nitric Oxide
31C4KY9ESH
Progesterone
4G7DS2Q64Y
Melatonin
JL5DK93RCL
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM