Extremely Low-Frequency Electromagnetic Field (ELF-EMF) Increases Mitochondrial Electron Transport Chain Activities and Ameliorates Depressive Behaviors in Mice.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
21 Oct 2024
Historique:
received: 08 09 2024
revised: 17 10 2024
accepted: 17 10 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 26 10 2024
Statut: epublish

Résumé

Compromised mitochondrial electron transport chain (ETC) activities are associated with depression in humans and rodents. However, the effects of the enhancement of mitochondrial ETC activities on depression remain elusive. We recently reported that an extremely low-frequency electromagnetic field (ELF-EMF) of as low as 10 μT induced hormetic activation of mitochondrial ETC complexes in human/mouse cultured cells and mouse livers. Chronic social defeat stress (CSDS) for 10 consecutive days caused behavioral defects mimicking depression in mice, and using an ELF-EMF for two to six weeks ameliorated them. CSDS variably decreased the mitochondrial ETC proteins in the prefrontal cortex (PFC) in 10 days, which were increased by an ELF-EMF in six weeks. CSDS had no effect on the mitochondrial oxygen consumption rate in the PFC in 10 days, but using an ELF-EMF for six weeks enhanced it. CSDS inactivated SOD2 by enhancing its acetylation and increased lipid peroxidation in the PFC. In contrast, the ELF-EMF activated the Sirt3-FoxO3a-SOD2 pathway and suppressed lipid peroxidation. Furthermore, CSDS increased markers for mitophagy, which was suppressed by the ELF-EMF in six weeks. The ELF-EMF exerted beneficial hormetic effects on mitochondrial energy production, mitochondrial antioxidation, and mitochondrial dynamics in a mouse model of depression. We envisage that an ELF-EMF is a promising therapeutic option for depression.

Identifiants

pubmed: 39457098
pii: ijms252011315
doi: 10.3390/ijms252011315
pii:
doi:

Substances chimiques

Superoxide Dismutase EC 1.15.1.1
Sirtuin 3 EC 3.5.1.-
superoxide dismutase 2 EC 1.15.1.1
Forkhead Box Protein O3 0
FoxO3 protein, mouse 0
Sirt3 protein, mouse 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Japan Society for the Promotion of Science
ID : JP23K18273
Organisme : Japan Society for the Promotion of Science
ID : JP23K06412
Organisme : Japan Society for the Promotion of Science
ID : JP23H02794
Organisme : Ministry of Health, Labour, and Welfare of Japan
ID : 23FC1014
Organisme : Intramural Research Grant for Neurological and Psychiatric Disorders of NCNP
ID : 5-6
Organisme : Murata Science and Education Foundation
ID : M23-107

Auteurs

Masaki Teranishi (M)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

Mikako Ito (M)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

Zhizhou Huang (Z)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

Yuki Nishiyama (Y)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

Akio Masuda (A)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

Hiroyuki Mino (H)

Division of Material Science (Physics), Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan.

Masako Tachibana (M)

Department of Psychiatry, Nagoya University Hospital, Nagoya 466-8560, Japan.

Toshiya Inada (T)

Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

Kinji Ohno (K)

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
Graduate School of Nutritional Sciences, Nagoya University of Arts and Sciences, Nisshin 470-0196, Japan.

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Classifications MeSH