Dietary conjugated linoleic acid downregulates the AlCl 3 -induced hyperactivation of compensatory and maladaptive signalling in the mouse brain cortex

• Published in: Free radical biology & medicine Vol. 213; p. 102
• Main Authors: Cuciniello, R, Luongo, D, Maurano, F, Crispi, S, Bergamo, P
• Format: Journal Article
• Language: English
• Published: United States 01-03-2024
• Subjects: Conjugated linoleic acid; Neuroprotection; Adaptive response; Nuclear erythroid-related factor 2; Alzheimer's disease; Endoplasmic reticulum stress; Unfolded protein response
• ISSN: 1873-4596

Oxidative stress, hyperactivation of compensatory mechanisms (unfolded protein response, UPR; nuclear factor erythroid 2-related factor 2, Nrf2) and the stimulation of maladaptive response (inflammation/apoptosis) are interconnected pathogenic processes occurring during Alzheimer's disease (AD) progression. The neuroprotective ability of dietary Conjugated linoleic acid (CLAmix) in a mouse model of AlCl
-induced AD was recently described but, the effects of AlCl
or CLAmix intake on these pathogenic processes are still unknown. The effects of dietary AlCl
or CLAmix - alone and in combination - were examined in the brain cortex of twenty-eight BalbC mice divided into 4 groups (n = 7 each). The neurotoxic effects of AlCl
were investigated in animals treated for 5 weeks with 100 mg/kg/day (AL). CLAmix supplementation (600 mg/kg bw/day) for 7 weeks (CLA) was aimed at evaluating its modulatory effects on the Nrf2 pathway while its co-treatment with AlCl
during the last 5 weeks of CLAmix intake (CLA + AL) was used to investigate its neuroprotective ability. Untreated mice were used as controls. In the CLA group, the NADPH oxidase (NOX) activation in the brain cortex was accompanied by the modulation of the Nrf2 pathway. By contrast, in the AL mice, the significant upregulation of oxidative stress markers, compensatory pathways (UPR/Nrf2), proinflammatory cytokines (IL-6, TNFα) and the proapoptotic protein Bax levels were found as compared with control. Notably, in CLA + AL mice, the marked decrease of oxidative stress, UPR/Nrf2 markers and proinflammatory cytokines levels were associated with the significant increase of the antiapoptotic protein Bcl2. The involvement of NOX in the adaptive response elicited by CLAmix along with its protective effects against the onset of several pathogenic processes triggered by AlCl
, broadens the knowledge of the mechanism underlying the pleiotropic activity of Nrf2 activators and sheds new light on their potential therapeutic use against neurodegenerative disorders.