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Curcumin Decreases Hippocampal Neurodegeneration and Nitro-Oxidative Damage to Plasma Proteins and Lipids Caused by Short-Term Exposure to Ozone

Neurodegeneration is the consequence of harmful events affecting the nervous system that lead to neuronal death. Toxic substances, including air pollutants, are capable of inducing neurodegeneration. Ozone (O(3)) is the most oxidative toxic pollutant. O(3) reacts with cellular components and forms r...

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Detalles Bibliográficos
Autores principales: Mendoza-Magaña, María Luisa, Espinoza-Gutiérrez, Hugo Alejandro, Nery-Flores, Sendar Daniel, Ramírez-Mendoza, Abraham Alberto, Cortez-Álvarez, Cesar Ricardo, Bonnet-Lemus, Robert de Mario, Ramírez-Herrera, Mario Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272084/
https://www.ncbi.nlm.nih.gov/pubmed/34279415
http://dx.doi.org/10.3390/molecules26134075
Descripción
Sumario:Neurodegeneration is the consequence of harmful events affecting the nervous system that lead to neuronal death. Toxic substances, including air pollutants, are capable of inducing neurodegeneration. Ozone (O(3)) is the most oxidative toxic pollutant. O(3) reacts with cellular components and forms reactive oxygen and nitrogen species, triggering nitro-oxidative damage during short-term exposure. Curcumin (CUR) is a natural phenolic molecule bearing well-documented antioxidant and anti-inflammatory biological activities in diverse experimental models. The aim of this work was to evaluate the effect of preventive dietary administration of CUR against hippocampal neurodegeneration and nitro-oxidative damage caused by short-term exposure to O(3). Eighty Wistar male rats were distributed into four experimental groups, twenty rats each: intact control; CUR dietary supplementation without O(3) exposure; exposure to 0.7 ppm of O(3); and exposed to O(3) with CUR dietary supplementation. Five rats from each group were sacrificed at 1, 2, 4, and 8 h of exposure. The CUR dose was 5.6 mg/kg and adjusted according to food consumption. CUR significantly decreased oxidative damage to plasma lipids and proteins, as well as neurodegeneration in CA1 and CA3 hippocampal regions. Concluding, CUR proved effective protection in decreasing neurodegeneration in the hippocampus and prevented systemic oxidative damage.