[Melatonin Induces Apoptotic Cell Death in 3T3-L1 Preadipocytes].


Journal

Molekuliarnaia biologiia
ISSN: 0026-8984
Titre abrégé: Mol Biol (Mosk)
Pays: Russia (Federation)
ID NLM: 0105454

Informations de publication

Date de publication:
Historique:
received: 07 12 2018
accepted: 13 05 2019
entrez: 12 5 2020
pubmed: 12 5 2020
medline: 20 8 2020
Statut: ppublish

Résumé

Obesity is a major disease that causes significant complications. Inhibition of preadipocyte proliferation has the potential to prevent obesity and metabolic diseases. Melatonin is a pineal gland hormone that has various effects on cells and tissues. In this research, we investigated whether melatonin induces apoptosis in 3T3-L1 preadipocytes. 3T3-L1 preadipocytes were cultured until confluence and then treated with 0, 10, 100, and 1000 μM melatonin for 1, 3, and 5 days. A cell viability assay kit was used for determining cell viability. Cell death marker proteins were assessed by Western blot analysis using GAPDH for control. Apoptotic morphological changes with nuclei fragmentation were observed using DAPI staining. Melatonin treatment decreased the phosphorylated extracellular signal-regulated kinases (p-ERK) activation while increasing the activation of caspase-3, 8, and 9. Furthermore, melatonin not only increased Bcl-2-associated X protein (Bax) but decreased B-cell lymphoma 2 (Bcl-2) expression as dose increases from 0 to 1000 μM. The melatonin treatment also suppressed the growth of preadipocytes with increasing concentration. These effects were attenuated by luzindole, a melatonin receptor antagonist and U0126, an inhibitor of p-ERK activation. In conclusion, melatonin can induce apoptosis of 3T3-L1 preadipocytes via p-ERK decrease.

Identifiants

pubmed: 32392192
doi: 10.31857/S0026898420020123
doi:

Substances chimiques

Bax protein, mouse 0
Proto-Oncogene Proteins c-bcl-2 0
bcl-2-Associated X Protein 0
Bcl2 protein, mouse 114100-40-2
Extracellular Signal-Regulated MAP Kinases EC 2.7.11.24
Caspases EC 3.4.22.-
Melatonin JL5DK93RCL

Types de publication

Journal Article

Langues

rus

Sous-ensembles de citation

IM

Pagination

233-243

Auteurs

J Lee (J)

Department of Biomedical Engineering, College of Health Science, Yonsei University, Wonju, Gangwon-do, 26493 Republic of Korea.

Y-M Yoo (YM)

Laboratory of Veterinary Biochemistry and Molecular Biology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk, 28644 Republic of Korea.

Y H Lee (YH)

Department of Biomedical Engineering, College of Health Science, Yonsei University, Wonju, Gangwon-do, 26493 Republic of Korea.

C H Kim (CH)

Department of Biomedical Engineering, College of Health Science, Yonsei University, Wonju, Gangwon-do, 26493 Republic of Korea.
chihyun@yonsei.ac.kr.

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Classifications MeSH