Department of Clinical Biochemistry, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, China.
Phytother Res. 2024 Oct;38(10):4923-4939. doi: 10.1002/ptr.7773. Epub 2023 Feb 15.
The preventive effect of saffron against Alzheimer's disease (AD) has been reported. Herein, we studied the effect of Cro and Crt, saffron carotenoids, on the cellular model of AD. The MTT assay, flow cytometry, and elevated p-JNK, p-Bcl-2, and c-PARP indicated the AβOs-induced apoptosis in differentiated PC12 cells. Then, the protective effects of Cro/Crt on dPC12 cells against AβOs were investigated in preventive and therapeutic modalities. Starvation was used as a positive control. RT-PCR and Western blot results revealed the reduced eIF2α phosphorylation and increased spliced-XBP1, Beclin1, LC3II, and p62, which indicate the AβOs-induced autophagic flux defect, autophagosome accumulation, and apoptosis. Cro and Crt inhibited the JNK-Bcl-2-Beclin1 pathway. They altered Beclin1 and LC3II and decreased p62 expressions, leading cells to survival. Cro and Crt altered the autophagic flux by different mechanisms. So, Cro increased the rate of autophagosome degradation more than Crt, while Crt increased the rate of autophagosome formation more than Cro. The application of 4μ8C and chloroquine as the inhibitors of XBP1 and autophagy, respectively, confirmed these results. So, augmentation of the survival branches of UPR and autophagy is involved and may serve as an effective strategy to prevent the progression of AβOs toxicity.
藏红花预防阿尔茨海默病(AD)的作用已有报道。在此,我们研究了藏红花类胡萝卜素 Cro 和 Crt 对 AD 细胞模型的影响。MTT 测定、流式细胞术和升高的 p-JNK、p-Bcl-2 和 c-PARP 表明 AβOs 诱导分化的 PC12 细胞凋亡。然后,以饥饿作为阳性对照,研究了 Cro/Crt 对 dPC12 细胞在预防和治疗模式下对 AβOs 的保护作用。RT-PCR 和 Western blot 结果显示,eIF2α 磷酸化减少, spliced-XBP1、Beclin1、LC3II 和 p62 增加,表明 AβOs 诱导自噬流缺陷、自噬体积累和凋亡。Cro 和 Crt 抑制了 JNK-Bcl-2-Beclin1 通路。它们改变了 Beclin1 和 LC3II 并降低了 p62 的表达,使细胞存活。Cro 和 Crt 通过不同的机制改变了自噬流。因此,Cro 增加了自噬体降解的速度,而 Crt 增加了自噬体形成的速度。应用 4μ8C 和氯喹分别作为 XBP1 和自噬的抑制剂,证实了这些结果。因此,UPR 和自噬的存活分支的增强可能参与其中,并可能成为预防 AβOs 毒性进展的有效策略。