Roberto Collado-Perez, David Chamoso-Sánchez, Antonia García, María S. Fernández-Alfonso, Maria Jiménez-Hernáiz, Sandra Canelles, Jesús Argente, Laura M. Frago, Julie A. Chowen
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Thus, we hypothesized that how hypothalamic astrocytes process-specific fatty acids participates in determining the differential metabolic response and that this is sex dependent as males and females respond differently to high-fat diets. Male and female primary hypothalamic astrocyte cultures were treated with oleic acid (OA) or palmitic acid (PA) for 24 h, and an untargeted metabolomics study was performed. A clear predictive model for PA exposure was obtained, while the metabolome after OA exposure was not different from controls. The observed modifications in metabolites, as well as the expression levels of key metabolic enzymes, indicate a reduction in the activity of the Krebs and glutamate/glutamine cycles in response to PA. In addition, there were specific differences between the response of astrocytes from male and female mice, as well as between hypothalamic and cerebral cortical astrocytes. 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引用次数: 0
摘要
与含有单一或不饱和脂肪的饮食相比,富含饱和脂肪的饮食更不利于健康。脂肪酸是重要的能量来源,但它们也向下丘脑代谢回路传递有关营养状况的信息,过量时会对这些回路造成损害。星形胶质细胞是中枢脂肪酸β氧化的主要场所,下丘脑星形胶质细胞参与能量平衡,部分是通过调节到达代谢神经元的激素和营养信号,以及参与对高脂肪饮食的炎症反应。因此,我们假设下丘脑星形胶质细胞如何处理特异性脂肪酸参与决定不同的新陈代谢反应,而这与性别有关,因为男性和女性对高脂肪饮食的反应不同。用油酸(OA)或棕榈酸(PA)处理男性和女性原代下丘脑星形胶质细胞培养物 24 小时,并进行非靶向代谢组学研究。结果表明,PA 暴露后的代谢组与对照组无差异,而OA 暴露后的代谢组则与对照组无差异。观察到的代谢物变化以及关键代谢酶的表达水平表明,克雷布斯循环和谷氨酸/谷氨酰胺循环的活性对 PA 的反应有所降低。此外,雄性小鼠和雌性小鼠的星形胶质细胞,以及下丘脑星形胶质细胞和大脑皮质星形胶质细胞的反应也存在特定差异。因此,下丘脑星形胶质细胞对特定脂肪酸的反应可能会对周围的代谢神经元产生不同的影响,从而导致不同的系统代谢结果。
The differential effects of palmitic acid and oleic acid on the metabolic response of hypothalamic astrocytes from male and female mice
Diets rich in saturated fats are more detrimental to health than those containing mono- or unsaturated fats. Fatty acids are an important source of energy, but they also relay information regarding nutritional status to hypothalamic metabolic circuits and when in excess can be detrimental to these circuits. Astrocytes are the main site of central fatty acid β-oxidation, and hypothalamic astrocytes participate in energy homeostasis, in part by modulating hormonal and nutritional signals reaching metabolic neurons, as well as in the inflammatory response to high-fat diets. Thus, we hypothesized that how hypothalamic astrocytes process-specific fatty acids participates in determining the differential metabolic response and that this is sex dependent as males and females respond differently to high-fat diets. Male and female primary hypothalamic astrocyte cultures were treated with oleic acid (OA) or palmitic acid (PA) for 24 h, and an untargeted metabolomics study was performed. A clear predictive model for PA exposure was obtained, while the metabolome after OA exposure was not different from controls. The observed modifications in metabolites, as well as the expression levels of key metabolic enzymes, indicate a reduction in the activity of the Krebs and glutamate/glutamine cycles in response to PA. In addition, there were specific differences between the response of astrocytes from male and female mice, as well as between hypothalamic and cerebral cortical astrocytes. Thus, the response of hypothalamic astrocytes to specific fatty acids could result in differential impacts on surrounding metabolic neurons and resulting in varied systemic metabolic outcomes.
期刊介绍:
The Journal of Neuroscience Research (JNR) publishes novel research results that will advance our understanding of the development, function and pathophysiology of the nervous system, using molecular, cellular, systems, and translational approaches. JNR covers both basic research and clinical aspects of neurology, neuropathology, psychiatry or psychology.
The journal focuses on uncovering the intricacies of brain structure and function. Research published in JNR covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of the nervous system, with emphasis on how disease modifies the function and organization.