Department of Anatomy, Histology and Embryology, School of Basic Medical Sciences, Fudan University, 138 Yi Xue Yuan Road, Shanghai, 200032, China.
Key Laboratory of Medical Imaging Computing and Computer Assisted Intervention of Shanghai, 138 Yi Xue Yuan Road, Shanghai, 200032, China.
Lipids. 2021 Jul;56(4):437-448. doi: 10.1002/lipd.12306. Epub 2021 May 31.
To investigate alterations of lipidomes in the progress of photoreceptor degeneration induced by N-methyl-N-nitrosourea (MNU) in a rat model, retinal lipid molecular species in adult Sprague-Dawley (SD) rats at 1, 3, and 7 days after MNU administration and age-matched controls were analyzed by the shotgun lipidomics technology. Moreover, total fatty acid levels in retinal, liver, and plasma samples of different groups were determined with gas chromatography. Generally, at day 1, the levels of ethanolamine plasmalogen species in retinas were markedly elevated after treatment with MNU, while the contents of other phospholipids and sphingolipids in the retina were not significantly changed than those of the control group. The compositions of almost all of unsaturated fatty acids in the retina increased significantly at day 1 after MNU administration. At day 7, the MNU treatment group has significant increases in lipid species in the retina. However, the majority of lipids containing docosahexaenoic acid (DHA, 22:6n-3) and docosapentaenoic acid (22:5n-6) declined, especially di-DHA phospholipids were dramatically reduced in the retina. In contrast, similar alterations did not occur in plasma or the liver after MNU treatment. These results suggested that at the early stage of photoreceptor degeneration, lipidome remodeling in the retina might involve protection of photoreceptor from apoptosis and continue their transduction of light. However, at the late stage of photoreceptor apoptosis, increases in comprehensive lipid species occurred, likely due to the myelination of the retina. Finally, the deficiency of DHA in photoreceptor degeneration could exacerbate the influence of myelination on retinal function. We further investigated the effects of unsaturated fatty acids on neuronal apoptosis. The preliminary experiments confirmed our observation from lipidomics analysis that unsaturated fatty acids can protect neurons from apoptosis. Collectively, our study suggests that increased levels of DHA should be protective from photoreceptor degeneration.
为了研究 N-甲基-N-亚硝脲(MNU)诱导的大鼠光感受器退行性变过程中脂类组的变化,采用 shotgun 脂质组学技术分析了 MNU 给药后 1、3 和 7 天成年 Sprague-Dawley(SD)大鼠视网膜的脂质分子种类,并与年龄匹配的对照组进行了比较。此外,还采用气相色谱法测定了不同组别的视网膜、肝脏和血浆样本中的总脂肪酸水平。总的来说,在第 1 天,MNU 处理后视网膜乙醇胺质体的水平明显升高,而其他磷脂和鞘脂的含量与对照组相比没有明显变化。MNU 给药后第 1 天,视网膜中几乎所有不饱和脂肪酸的组成都显著增加。在第 7 天,MNU 处理组的视网膜中脂质种类显著增加。然而,含有二十二碳六烯酸(DHA,22:6n-3)和二十二碳五烯酸(22:5n-6)的大多数脂质含量下降,特别是二-DHA 磷脂在视网膜中显著减少。相比之下,MNU 处理后血浆或肝脏中没有发生类似的变化。这些结果表明,在光感受器退行性变的早期阶段,视网膜的脂类组重构可能涉及保护光感受器免受细胞凋亡,并继续进行光转导。然而,在光感受器细胞凋亡的晚期阶段,综合脂质种类增加,可能是由于视网膜的髓鞘形成。最后,光感受器退行性变中 DHA 的缺乏可能会加剧髓鞘形成对视网膜功能的影响。我们进一步研究了不饱和脂肪酸对神经元凋亡的影响。初步实验证实了我们从脂质组学分析中观察到的结果,即不饱和脂肪酸可以保护神经元免受细胞凋亡。综上所述,我们的研究表明,增加 DHA 的水平可能对光感受器退行性变具有保护作用。