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萝卜硫素通过调节抗氧化反应在内质网稳态中的作用。

Role of sulforaphane in endoplasmic reticulum homeostasis through regulation of the antioxidant response.

作者信息

Dana Arana-Hidalgo, Alejandro Silva-Palacios

机构信息

Department of Cardiovascular Biomedicine, National Institute of Cardiology Ignacio Chávez, Mexico City, Mexico.

Department of Cardiovascular Biomedicine, National Institute of Cardiology Ignacio Chávez, Mexico City, Mexico.

出版信息

Life Sci. 2022 Jun 15;299:120554. doi: 10.1016/j.lfs.2022.120554. Epub 2022 Apr 19.

DOI:10.1016/j.lfs.2022.120554
PMID:35452639
Abstract

Nowadays, the nutraceutical agent sulforaphane (SFN) shows great versatility in turning on different cellular responses. Mainly, this isothiocyanate acts as a master regulator of cellular homeostasis due to its antioxidant response and cytoplasmic, mitochondrial, and endoplasmic reticulum (ER) protein modulation. Even more, SFN acts as an effective strategy to counteract oxidative stress, apoptosis, and ER stress, among others as seen in different injury models. Particularly, ER stress is buffered by the unfolded protein response (UPR) activation, which is the first instance in orchestrating the recovery of ER function. Interestingly, different studies highlight a close interrelationship between ER stress and oxidative stress, two events driven by the accumulation of reactive oxygen species (ROS). This response inevitably perpetuates itself and acts as a vicious cycle that triggers the development of different pathologies, such as cardiovascular diseases, neurodegenerative diseases, and others. Accordingly, it is vital to target ER stress and oxidative stress to increase the effectiveness of clinical therapies used to treat these diseases. Therefore, our study is focused on the role of SFN in preserving cellular homeostasis balance by regulating the ER stress response through the Nrf2-modulated antioxidant pathway.

摘要

如今,营养保健品萝卜硫素(SFN)在引发不同细胞反应方面展现出极大的多功能性。主要而言,这种异硫氰酸盐由于其抗氧化反应以及对细胞质、线粒体和内质网(ER)蛋白质的调节作用,充当着细胞稳态的主要调节因子。此外,在不同的损伤模型中可以看到,SFN是对抗氧化应激、细胞凋亡和内质网应激等的有效策略。特别是,内质网应激通过未折叠蛋白反应(UPR)的激活得到缓冲,这是协调内质网功能恢复的首要环节。有趣的是,不同研究强调了内质网应激与氧化应激之间的密切相互关系,这两个事件均由活性氧(ROS)的积累所驱动。这种反应不可避免地会自我延续,并形成一个恶性循环,引发诸如心血管疾病、神经退行性疾病等不同病理状况的发展。因此,针对内质网应激和氧化应激以提高用于治疗这些疾病的临床疗法的有效性至关重要。所以,我们的研究聚焦于SFN通过Nrf2调节的抗氧化途径调控内质网应激反应,从而在维持细胞稳态平衡中所起的作用。

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