Drug Discovery and Development, Istituto Italiano di Tecnologia, Via Morego 30, I-16163 Genova, Italy.
Department of Anatomy and Neurobiology, University of California, Irvine, CA 92697, United States; Department of Biological Chemistry, University of California, Irvine, CA 92697, United States; Department of Pharmacology, University of California, Irvine, CA 92697, United States.
Biochim Biophys Acta Mol Cell Biol Lipids. 2017 Dec;1862(12):1502-1511. doi: 10.1016/j.bbalip.2017.08.008. Epub 2017 Aug 30.
Sphingolipids have been implicated in age-related neurodegeneration. Previous studies have reported elevated ceramide levels in the brain of old rodents, but a systematic investigation of the impact of age on brain sphingolipid metabolism is still lacking. Here we quantified 17 key sphingolipid species in the hippocampus of young (3months), middle-aged (12months) and old (21months) male and female mice. Lipids were extracted and quantified by liquid chromatography/mass spectrometry; transcription of enzymes involved in sphingolipid biosynthesis was evaluated by qPCR. Age-dependent changes of multiple sphingolipid species - including ceramide (d18:1/18:0), sphingomyelin (d34:1), hexosylceramide (d18:1/16:0), ceramide (d18:1/24:0) - were found in mice of both sexes. Moreover, sex-dependent changes were seen with hexosylceramide (d18:1/18:0), ceramide (d18:1/22:0), sphingomyelin (d36:1) and sphingomyelin (d42:1). Importantly, an age-dependent accumulation of sphingolipids containing nervonic acid (24:1) was observed in 21month-old male (p=0.04) and female mice (p<0.0001). Consistent with this increase, transcription of the nervonic acid-synthesizing enzyme, stearoyl-CoA desaturase (Scd1 and Scd2), was upregulated in 21month-old female mice (Scd1 p=0.006; Scd2 p=0.009); a similar trend was observed in males (Scd1 p=0.07). In conclusion, the results suggest that aging is associated with profound sex-dependent and -independent changes in hippocampal sphingolipid profile. The results also highlight the need to examine the contribution of sphingolipids, and particularly of those containing nervonic acid, in normal and pathological brain aging.
鞘脂类化合物与年龄相关的神经退行性变有关。以前的研究报告称,老年啮齿动物大脑中的神经酰胺水平升高,但对年龄对大脑鞘脂代谢的影响仍缺乏系统的研究。在这里,我们定量检测了年轻(3 个月)、中年(12 个月)和老年(21 个月)雄性和雌性小鼠海马体中 17 种关键鞘脂。通过液相色谱/质谱法提取和定量脂质;通过 qPCR 评估参与鞘脂生物合成的酶的转录。在两性小鼠中发现了多种鞘脂(包括神经酰胺(d18:1/18:0)、神经鞘磷脂(d34:1)、己糖神经酰胺(d18:1/16:0)、神经酰胺(d18:1/24:0))的年龄依赖性变化。此外,还观察到两性之间的性别依赖性变化,包括己糖神经酰胺(d18:1/18:0)、神经酰胺(d18:1/22:0)、神经鞘磷脂(d36:1)和神经鞘磷脂(d42:1)。重要的是,在 21 个月大的雄性(p=0.04)和雌性(p<0.0001)小鼠中观察到含有神经酸(24:1)的鞘脂的年龄依赖性积累。与这种增加一致,21 个月大的雌性小鼠中神经酸合成酶硬脂酰辅酶 A 去饱和酶(Scd1 和 Scd2)的转录上调(Scd1 p=0.006;Scd2 p=0.009);在雄性中也观察到类似的趋势(Scd1 p=0.07)。总之,研究结果表明,衰老与海马鞘脂谱的深刻的性别依赖和非性别依赖变化有关。研究结果还强调了需要检查鞘脂,特别是含有神经酸的鞘脂,在正常和病理性脑衰老中的作用。