Diet-Induced Obesity in the Rat Impairs Sphingolipid Metabolism in the Brain and This Metabolic Dysfunction Is Transmitted to the Offspring via Both the Maternal and the Paternal Lineage.

IF 4.2 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Neurochemistry Pub Date : 2025-01-01 DOI:10.1111/jnc.16307
Juan Antonio García Santillán, Carla Elena Mezo-González, Mathilde Gourdel, Mikaël Croyal, Francisco Bolaños-Jiménez
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Abstract

Obesity leads to a number of health problems, including learning and memory deficits that can be passed on to the offspring via a developmental programming process. However, the mechanisms involved in the deleterious effects of obesity on cognition remain largely unknown. This study aimed to assess the impact of obesity on the production of sphingolipids (ceramides and sphingomyelins) in the brain and its relationship with the learning deficits displayed by obese individuals. We also sought to determine whether the effects of obesity on brain sphingolipid synthesis could be passed on to the offspring. Learning abilities and brain concentration of sphingolipids in male and female control and obese founder rats (F0) and their offspring (F1) were evaluated, respectively, by the novel object recognition test and by ultra-performance liquid chromatography tandem mass spectrometry. In addition, a global lipidome profiling of the cerebral cortex and hippocampus was performed. Both male and female F0 rats showed impaired learning and increased concentrations of ceramides and sphingomyelins in the hippocampus and frontal cortex compared to their control counterparts. However, the overall lipidome profile of these brain regions did not change with obesity. Remarkably, the alterations in brain sphingolipid synthesis, as well as the cognitive impairment induced by obesity, were also present in adult F1 male rats born to obese mothers or sired by obese fathers and were associated with enhanced expression of mRNAs coding for enzymes involved in the de novo synthesis of ceramides. These results show that the cognitive deficits and impaired sphingolipid metabolism induced by obesity can be transmitted to the offspring through both the maternal and paternal lineages and suggest that an increase in the brain concentration of sphingolipids could play a causal role in the cognitive deficits associated with obesity.

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饮食引起的肥胖损害大鼠大脑鞘脂代谢,这种代谢功能障碍通过母系和父系遗传给后代。
肥胖会导致一系列健康问题,包括学习和记忆缺陷,这些问题可能会通过发育程序传递给后代。然而,肥胖对认知的有害影响的机制在很大程度上仍然未知。本研究旨在评估肥胖对大脑中鞘脂(神经酰胺和鞘磷脂)产生的影响及其与肥胖个体表现出的学习缺陷的关系。我们还试图确定肥胖对脑鞘脂合成的影响是否会遗传给后代。采用新型目标识别法和超高效液相色谱串联质谱法分别测定雄性、雌性对照大鼠和肥胖始祖大鼠(F0)及其后代(F1)的学习能力和脑鞘脂浓度。此外,还进行了大脑皮层和海马体的全球脂质组分析。与对照组相比,雄性和雌性F0大鼠的学习能力受损,海马和额叶皮层的神经酰胺和鞘鞘磷脂浓度增加。然而,这些大脑区域的总体脂质谱并没有随着肥胖而改变。值得注意的是,脑鞘脂合成的改变,以及肥胖引起的认知障碍,也存在于肥胖母亲所生或肥胖父亲所生的成年F1雄性大鼠中,并且与编码神经酰胺新生合成酶的mrna表达增强有关。这些结果表明,肥胖引起的认知缺陷和鞘脂代谢受损可以通过母系和父系遗传给后代,并提示大脑鞘脂浓度的增加可能在肥胖相关的认知缺陷中起因果作用。
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来源期刊
Journal of Neurochemistry
Journal of Neurochemistry 医学-神经科学
CiteScore
9.30
自引率
2.10%
发文量
181
审稿时长
2.2 months
期刊介绍: Journal of Neurochemistry focuses on molecular, cellular and biochemical aspects of the nervous system, the pathogenesis of neurological disorders and the development of disease specific biomarkers. It is devoted to the prompt publication of original findings of the highest scientific priority and value that provide novel mechanistic insights, represent a clear advance over previous studies and have the potential to generate exciting future research.
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