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Lutein/zeaxanthin isomers regulate neurotrophic factors and synaptic plasticity in trained rats

BACKGROUND/AIM: This study was conducted to elucidate the effects of lutein/zeaxanthin isomers (L/Zi) on lipid metabolism, oxidative stress, NF-κB/Nrf2 pathways, and synaptic plasticity proteins in trained rats. MATERIALS AND METHODS: Wistar rats were distributed into four groups: 1) control, 2) L/Z...

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Detalles Bibliográficos
Autores principales: ORHAN, Cemal, ERTEN, Füsun, ER, Beşir, TUZCU, Mehmet, ŞAHİN, Nurhan, DURMAZ KURŞUN, Öznur Ece, JUTURU, Vijaya, ŞAHİN, Kazim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573940/
https://www.ncbi.nlm.nih.gov/pubmed/33843170
http://dx.doi.org/10.3906/sag-2101-264
Descripción
Sumario:BACKGROUND/AIM: This study was conducted to elucidate the effects of lutein/zeaxanthin isomers (L/Zi) on lipid metabolism, oxidative stress, NF-κB/Nrf2 pathways, and synaptic plasticity proteins in trained rats. MATERIALS AND METHODS: Wistar rats were distributed into four groups: 1) control, 2) L/Zi: rats received L/Zi at the dose of 100 mg/kg by oral gavage, 3) exercise, 4) exercise+L/Zi: rats exercised and received L/Zi (100 mg/kg) by oral gavage. The duration of the study was eight weeks. RESULTS: Exercise combined with L/Zi reduced lipid peroxidation and improved antioxidant enzyme activities of muscle and cerebral cortex in rats (p < 0.001). In the Exercise + L/Zi group, muscle and cerebral cortex Nrf2 and HO-1 levels increased, while NF-κB levels decreased (p <0.001). Also, L/Zi improved BDNF, synapsin I, SYP, and GAP-43 levels of the cerebral cortex of trained rats (p < 0.001). The highest levels of BDNF, synapsin SYP, and GAP-43 in the cerebral cortex were determined in the Exercise+L/Zi group. CONCLUSION: These results suggested that exercise combined with L/Zi supplementation might be effective to reduce neurodegeneration via improving neurotrophic factors and synaptic proteins, and oxidative capacity in the cerebral cortex.