Glucose 6 phosphate dehydrogenase overexpression rescues the loss of cognition in the double transgenic APP/PS1 mouse model of Alzheimer’s disease

Correas, Ángela G. ; Olaso-Gonzalez, Gloria ; Roca, Marta ; Blanco-Gandía, Mari Carmen (Universidad de Zaragoza) ; Nascimento, Carla ; Lahoz, Agustín ; Rodríguez-Arias, Marta ; Miñarro, José ; Gómez-Cabrera, Mari Carmen ; Viña, José

Resumen: Mice models of Alzheimer's disease (APP/PS1) typically experience cognitive decline with age. G6PD overexpressing mice (G6PD-Tg) exhibit better protection from age-associated functional decline including improvements in metabolic and muscle functions as well as reduced frailty compared to their wild-type counterparts. Importantly G6PD-Tg mice show diminished accumulation of DNA oxidation in the brain at different ages in both males and females. To further explore the potential benefits of modulating the G6PD activity in neurodegenerative diseases, triple transgenic mice (3xTg G6PD) were generated, overexpressing APP, PSEN1, and G6PD genes. The cognitive decline characteristic of APP/PS1 mice was prevented in 3xTg G6PD mice, despite similar amyloid-β (Aβ) levels in the hippocampus. This challenges the dominant hypothesis in Alzheimer's disease (AD) etiology and the majority of therapeutic efforts in the field, based on the notion that Aβ is pivotal in cognitive preservation. Notably, the antioxidant properties of G6PD led to a decrease in oxidative stress parameters, such as improved GSH/GSSG and GSH/CysSSG ratios, without major changes in oxidative damage markers. Additionally, metabolic changes in 3xTg G6PD mice increased brain energy status, countering the hypometabolism observed in Alzheimer's models. Remarkably, a higher respiratory exchange ratio suggested increased carbohydrate utilization. The relative failures of Aβ-targeted clinical trials have raised significant skepticism on the amyloid cascade hypothesis and whether the development of Alzheimer's drugs has followed the correct path. Our findings highlight the significance of targeting glucose-metabolizing enzymes rather than solely focusing on Aβ in Alzheimer's research, advocating for a deeper exploration of glucose metabolism's role in cognitive preservation.

Idioma: Inglés

DOI: 10.1016/j.redox.2024.103242

Año: 2024

Publicado en: Redox Biology 75 (2024), 103242 [12 pp.]
ISSN: 2213-2317

Factor impacto JCR: 11.9 (2024)

Categ. JCR: BIOCHEMISTRY & MOLECULAR BIOLOGY rank: 15 / 319 = 0.047 (2024) - Q1 - T1

Factor impacto SCIMAGO: 3.374 - Biochemistry (Q1) - Organic Chemistry (Q1) - Clinical Biochemistry (Q1)

Financiación: info:eu-repo/grantAgreement/ES/AEI/PID2022-142470OB-I00
Financiación: info:eu-repo/grantAgreement/ES/AEI/RED2022-134800-T
Financiación: info:eu-repo/grantAgreement/EC/H2020/825546/EU/Scaling-up of and evidence-based intervention programme in older people with Diabetes and Frailty in LatinAmerica/DIABFRAIL-LATAM
Financiación: info:eu-repo/grantAgreement/ES/MICINN/ISCIII CB16-10-00435

Tipo y forma: Article (Published version)

Área (Departamento): Área Psicolog.Evolut.Educac (Dpto. Psicología y Sociología)