Protective effect of saffron carotenoids against amyloid beta-induced neurotoxicity in differentiated PC12 cells via the unfolded protein response and autophagy.

IF 6.1 2区 医学 Q1 CHEMISTRY, MEDICINAL Phytotherapy Research Pub Date : 2024-10-01 Epub Date: 2023-02-15 DOI:10.1002/ptr.7773
Mariam Sanjari-Pour, Nassim Faridi, Ping Wang, S Zahra Bathaie
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Abstract

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.

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藏红花类胡萝卜素通过未折叠蛋白反应和自噬对分化PC12细胞中淀粉样β诱导的神经毒性具有保护作用
藏红花对阿尔茨海默病(AD)的预防作用已有报道。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 试验、流式细胞术以及 p-JNK、p-Bcl-2 和 c-PARP 的升高表明 AβOs 诱导了分化 PC12 细胞的凋亡。然后,研究了 Cro/Crt 对 dPC12 细胞 AβOs 的预防和治疗作用。饥饿作为阳性对照。RT-PCR和Western印迹结果显示,eIF2α磷酸化减少,剪接-XBP1、Beclin1、LC3II和p62增加,这表明AβOs诱导的自噬通量缺陷、自噬体积累和细胞凋亡。Cro 和 Crt 可抑制 JNK-Bcl-2-Beclin1 通路。它们改变了 Beclin1 和 LC3II,减少了 p62 的表达,使细胞得以存活。Cro和Crt通过不同的机制改变自噬通量。因此,Cro比Crt更能提高自噬体的降解率,而Crt比Cro更能提高自噬体的形成率。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,增强 UPR 和自噬的存活分支可能是防止 AβOs 毒性恶化的有效策略。
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来源期刊
Phytotherapy Research
Phytotherapy Research 医学-药学
CiteScore
12.80
自引率
5.60%
发文量
325
审稿时长
2.6 months
期刊介绍: Phytotherapy Research is an internationally recognized pharmacological journal that serves as a trailblazing resource for biochemists, pharmacologists, and toxicologists. We strive to disseminate groundbreaking research on medicinal plants, pushing the boundaries of knowledge and understanding in this field. Our primary focus areas encompass pharmacology, toxicology, and the clinical applications of herbs and natural products in medicine. We actively encourage submissions on the effects of commonly consumed food ingredients and standardized plant extracts. We welcome a range of contributions including original research papers, review articles, and letters. By providing a platform for the latest developments and discoveries in phytotherapy, we aim to support the advancement of scientific knowledge and contribute to the improvement of modern medicine.
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