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Effect of the combination of different therapies on oxidative stress in the experimental model of multiple sclerosis

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Author
Escribano, Begoña M.
Muñoz Jurado, Ana
Luque, Evelio
Galván, Alberto
Latorre, Manuel
Caballero-Villarraso, Javier
Giraldo, Ana I.
Agüera, Eduardo
Túnez, Isaac
Publisher
IBRO
Date
2023
Subject
Oxidative stress
Experimental autoimmune encephalomyelitis
S-allylcysteine
Extra-virgin olive oil
Transcranial magnetic stimulation
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Abstract
Oxidative stress is heavily involved in several pathological features of Multiple Sclerosis (MS), such as myelin destruction, axonal degeneration, and inflammation. Different therapies have been shown to reduce the oxidative stress that occurs in the animal model of MS, experimental autoimmune encephalomyelitis (EAE). Some of these therapies are transcranial magnetic stimulation (TMS), extra virgin olive oil (EVOO) and S-allyl cysteine (SAC). This study aims to test the antioxidant effect of these three therapies, to compare the efficacy of SAC versus TMS and EVOO, and to analyze the effect of combining SAC + TMS and SAC and EVOO. Seventy Dark Agouti rats were used, which were divided into Control group; Vehicle group; Mock group; SAC; EVOO; TMS; SAC + EVOO; SAC + TMS; EAE; EAE + SAC; EAE + EVOO; EAE + TMS; EAE + SAC + EVOO; EAE + SAC + TMS. The TMS consisted of an oscillatory magnetic field in the form of a sine wave with a frequency of 60 Hz and an amplitude of 0.7mT (EL-EMF) applied for two hours in the morning, once a day, five days a week. SAC was administered at a dose of 50 mg/kg body weight, orally daily, five days a week. EVOO represented 10% of their calorie intake in the total standard daily diet of rats AIN-93G. All treatments were maintained for 51 days. TMS, EVOO and SAC, alone or in combination, reduce oxidative stress, increasing antioxidant defenses and also lowering the clinical score. Combination therapies do not appear to be more potent than individual therapies against the oxidative stress of EAE or its clinical symptoms.
Description
Embargado hasta 01/01/2100
URI
http://hdl.handle.net/10396/27170
Fuente
Neuroscience, Vol 529, Pages 116-128 (2023)
Versión del Editor
https://doi.org/10.1016/j.neuroscience.2023.08.005
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