Berdún Rebeca, Obis Èlia, Mota-Martorell Natàlia, Bassols Anna, Valent Daniel, Serrano José C E, Martín-Garí Meritxell, Rodríguez-Palmero María, Moreno-Muñoz José Antonio, Tibau Joan, Quintanilla Raquel, Pamplona Reinald, Portero-Otín Manuel, Jové Mariona
Department of Experimental Medicine, Lleida Biomedical Research Institute (IRBLleida), University of Lleida (UdL), 25198 Lleida, Spain.
Departament de Bioquímica i Biologia Molecular, Facultat de Veterinària, Universitat Autònoma de Barcelona, 08025 Barcelona, Spain.
Antioxidants (Basel). 2024 Jan 26;13(2):161. doi: 10.3390/antiox13020161.
Obesity is a risk factor for highly prevalent age-related neurodegenerative diseases, the pathogenesis of whichinvolves mitochondrial dysfunction and protein oxidative damage. Lipoxidation, driven by high levels of peroxidizable unsaturated fatty acids and low antioxidant protection of the brain, stands out as a significant risk factor. To gain information on the relationship between obesity and brain molecular damage, in a porcine model of obesity we evaluated (1) the level of mitochondrial respiratory chain complexes, as the main source of free radical generation, by Western blot; (2) the fatty acid profile by gas chromatography; and (3) the oxidative modification of proteins by mass spectrometry. The results demonstrate a selectively higher amount of the lipoxidation-derived biomarker malondialdehyde-lysine (MDAL) (34% increase) in the frontal cortex, and positive correlations between MDAL and LDL levels and body weight. No changes were observed in brain fatty acid profile by the high-fat diet, and the increased lipid peroxidative modification was associated with increased levels of mitochondrial complex I (NDUFS3 and NDUFA9 subunits) and complex II (flavoprotein). Interestingly, introducing n3 fatty acids and a probiotic in the high-fat diet prevented the observed changes, suggesting that dietary components can modulate protein oxidative modification at the cerebral level and opening new possibilities in neurodegenerative diseases' prevention.
肥胖是高发性年龄相关性神经退行性疾病的一个风险因素,其发病机制涉及线粒体功能障碍和蛋白质氧化损伤。在高水平的可过氧化不饱和脂肪酸和大脑低抗氧化保护作用的驱动下,脂氧化成为一个重要的风险因素。为了获取有关肥胖与脑分子损伤之间关系的信息,在一个肥胖猪模型中,我们评估了:(1)通过蛋白质印迹法检测作为自由基主要产生来源的线粒体呼吸链复合物的水平;(2)通过气相色谱法检测脂肪酸谱;(3)通过质谱法检测蛋白质的氧化修饰。结果表明,额叶皮质中脂氧化衍生生物标志物丙二醛 - 赖氨酸(MDAL)的含量选择性地更高(增加34%),并且MDAL与低密度脂蛋白水平和体重之间呈正相关。高脂饮食未观察到脑脂肪酸谱的变化,脂质过氧化修饰增加与线粒体复合物I(NDUFS3和NDUFA9亚基)和复合物II(黄素蛋白)水平升高有关。有趣的是,在高脂饮食中添加n3脂肪酸和益生菌可防止观察到的变化,这表明饮食成分可在大脑水平调节蛋白质氧化修饰,并为神经退行性疾病的预防开辟了新的可能性。