Age-Dependent Vulnerability to Oxidative Stress of Postnatal Rat Pyramidal Motor Cortex Neurons.

amyotrophic lateral sclerosis glutathione levels in the brain membrane excitability motor cortex oxidative stress postnatal development

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
19 Dec 2020
Historique:
received: 16 11 2020
revised: 14 12 2020
accepted: 15 12 2020
entrez: 23 12 2020
pubmed: 24 12 2020
medline: 24 12 2020
Statut: epublish

Résumé

Oxidative stress is one of the main proposed mechanisms involved in neuronal degeneration. To evaluate the consequences of oxidative stress on motor cortex pyramidal neurons during postnatal development, rats were classified into three groups: Newborn (P2-P7); infantile (P11-P15); and young adult (P20-P40). Oxidative stress was induced by 10 µM of cumene hydroperoxide (CH) application. In newborn rats, using the whole cell patch-clamp technique in brain slices, no significant modifications in membrane excitability were found. In infantile rats, the input resistance increased and rheobase decreased due to the blockage of GABAergic tonic conductance. Lipid peroxidation induced by CH resulted in a noticeable increase in protein-bound 4-hidroxynonenal in homogenates in only infantile and young adult rat slices. Interestingly, homogenates of newborn rat brain slices showed the highest capacity to respond to oxidative stress by dramatically increasing their glutathione and free thiol content. This increase correlated with a time-dependent increase in the glutathione reductase activity, suggesting a greater buffering capacity of newborn rats to resist oxidative stress. Furthermore, pre-treatment of the slices with glutathione monoethyl ester acted as a neuroprotector in pyramidal neurons of infantile rats. We conclude that during maturation, the vulnerability to oxidative stress in rat motor neurons increases with age.

Identifiants

pubmed: 33352810
pii: antiox9121307
doi: 10.3390/antiox9121307
pmc: PMC7766683
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Ministerio de Ciencia, Innovación y Universidades
ID : RTI2018-099908-B-C21
Organisme : Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía
ID : FEDER-UCA18-106647

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Auteurs

Livia Carrascal (L)

Departament of Physiology, Pharmacy School, University of Seville, 41012 Seville, Spain.
Biomedical Research and Innovation Institute of Cadiz (INIBICA), 11003 Cadiz, Spain.

Ella Gorton (E)

Departament of Physiology, Pharmacy School, University of Seville, 41012 Seville, Spain.

Ricardo Pardillo-Díaz (R)

Area of Physiology, School of Medicine, University of Cádiz, 11003 Cadiz, Spain.
Biomedical Research and Innovation Institute of Cadiz (INIBICA), 11003 Cadiz, Spain.

Patricia Perez-García (P)

Departament of Physiology, Pharmacy School, University of Seville, 41012 Seville, Spain.

Ricardo Gómez-Oliva (R)

Area of Physiology, School of Medicine, University of Cádiz, 11003 Cadiz, Spain.
Biomedical Research and Innovation Institute of Cadiz (INIBICA), 11003 Cadiz, Spain.

Carmen Castro (C)

Area of Physiology, School of Medicine, University of Cádiz, 11003 Cadiz, Spain.
Biomedical Research and Innovation Institute of Cadiz (INIBICA), 11003 Cadiz, Spain.

Pedro Nunez-Abades (P)

Departament of Physiology, Pharmacy School, University of Seville, 41012 Seville, Spain.
Biomedical Research and Innovation Institute of Cadiz (INIBICA), 11003 Cadiz, Spain.

Classifications MeSH