Department of Neuroendocrinology, Centre of Postgraduate Medical Education, Marymoncka 99/103, 01-813 Warsaw, Poland.
Department of Physiological Sciences, Institute of Veterinary Medicine, Warsaw University of Life Sciences (SGGW), Nowoursynowska 159, 02-776 Warsaw, Poland.
Oxid Med Cell Longev. 2020 Aug 5;2020:8908901. doi: 10.1155/2020/8908901. eCollection 2020.
Alzheimer's disease (AD) is the most common neurodegenerative disorder. Amyloid - (A-) induced mitochondrial dysfunction may be a primary process triggering all the cascades of events that lead to AD. Therefore, identification of natural factors and endogenous mechanisms that protect neurons against A toxicity is needed. In the current study, we investigated whether alpha-linolenic acid (ALA), as a natural product, would increase insulin and IGF-I (insulin-like growth factor I) release from astrocytes. Moreover, we explored the protective effect of astrocytes-derived insulin/IGF-I on A-induced neurotoxicity, with special attention paid to their impact on mitochondrial function of differentiated SH-SY5Y cells. The results showed that ALA induced insulin and IGF-I secretion from astrocytes. Our findings demonstrated that astrocyte-derived insulin/insulin-like growth factor I protects differentiated SH-SY5Y cells against A -induced cell death. Moreover, pretreatment with conditioned medium (CM) and ALA-preactivated CM (ALA-CM) protected the SH-SY5Y cells against A -induced mitochondrial dysfunction by reducing the depolarization of the mitochondrial membrane, increasing mitochondrial biogenesis, restoring the balance between fusion and fission processes, and regulation of mitophagy and autophagy processes. Our study suggested that astrocyte-derived insulin/insulin-like growth factor I suppresses A -induced cytotoxicity in the SH-SY5Y cells by protecting against mitochondrial dysfunction. Moreover, the neuroprotective effects of CM were intensified by preactivation with ALA.
阿尔茨海默病(AD)是最常见的神经退行性疾病。淀粉样蛋白(A)诱导的线粒体功能障碍可能是触发导致 AD 的所有级联事件的主要过程。因此,需要确定保护神经元免受 A 毒性的天然因素和内源性机制。在当前的研究中,我们研究了α-亚麻酸(ALA)是否作为天然产物会增加星形胶质细胞中胰岛素和 IGF-I(胰岛素样生长因子 I)的释放。此外,我们还探讨了星形胶质细胞衍生的胰岛素/IGF-I 对 A 诱导的神经毒性的保护作用,特别关注它们对分化的 SH-SY5Y 细胞中线粒体功能的影响。结果表明,ALA 诱导星形胶质细胞中胰岛素和 IGF-I 的分泌。我们的研究结果表明,星形胶质细胞衍生的胰岛素/胰岛素样生长因子 I 可保护分化的 SH-SY5Y 细胞免受 A 诱导的细胞死亡。此外,用条件培养基(CM)和 ALA 预激活 CM(ALA-CM)预处理可通过减少线粒体膜去极化、增加线粒体生物发生、恢复融合和分裂过程之间的平衡以及调节线粒体自噬和自噬过程来保护 SH-SY5Y 细胞免受 A 诱导的线粒体功能障碍。我们的研究表明,星形胶质细胞衍生的胰岛素/胰岛素样生长因子 I 通过防止线粒体功能障碍来抑制 SH-SY5Y 细胞中 A 诱导的细胞毒性。此外,通过 ALA 预激活,CM 的神经保护作用得到增强。