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SIRT3激活剂厚朴酚通过调节淀粉样蛋白生成途径减轻β-淀粉样蛋白。

SIRT3 activator Honokiol attenuates β-Amyloid by modulating amyloidogenic pathway.

作者信息

Ramesh Sindhu, Govindarajulu Manoj, Lynd Tyler, Briggs Gwyneth, Adamek Danielle, Jones Ellery, Heiner Jake, Majrashi Mohammed, Moore Timothy, Amin Rajesh, Suppiramaniam Vishnu, Dhanasekaran Muralikrishnan

机构信息

Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, Auburn, AL, United States of America.

出版信息

PLoS One. 2018 Jan 11;13(1):e0190350. doi: 10.1371/journal.pone.0190350. eCollection 2018.

Abstract

Honokiol (poly-phenolic lignan from Magnolia grandiflora) is a Sirtuin-3 (SIRT3) activator which exhibit antioxidant activity and augment mitochondrial functions in several experimental models. Modern evidence suggests the critical role of SIRT3 in the progression of several metabolic and neurodegenerative diseases. Amyloid beta (Aβ), the precursor to extracellular senile plaques, accumulates in the brains of patients with Alzheimer's disease (AD) and is related to the development of cognitive impairment and neuronal cell death. Aβ is generated from amyloid-β precursor protein (APP) through sequential cleavages, first by β-secretase and then by γ-secretase. Drugs modulating this pathway are believed to be one of the most promising strategies for AD treatment. In the present study, we found that Honokiol significantly enhanced SIRT3 expression, reduced reactive oxygen species generation and lipid peroxidation, enhanced antioxidant activities, and mitochondrial function thereby reducing Aβ and sAPPβ levels in Chinese Hamster Ovarian (CHO) cells (carrying the amyloid precursor protein-APP and Presenilin PS1 mutation). Mechanistic studies revealed that Honokiol affects neither protein levels of APP nor α-secretase activity. In contrast, Honokiol increased the expression of AMPK, CREB, and PGC-1α, thereby inhibiting β-secretase activity leading to reduced Aβ levels. These results suggest that Honokiol is an activator of SIRT3 capable of improving antioxidant activity, mitochondrial energy regulation, while decreasing Aβ, thereby indicating it to be a lead compound for AD drug development.

摘要

厚朴酚(来自厚朴的多聚酚木脂素)是一种沉默调节蛋白3(SIRT3)激活剂,在多个实验模型中表现出抗氧化活性并增强线粒体功能。现代证据表明SIRT3在几种代谢性和神经退行性疾病的进展中起关键作用。淀粉样β蛋白(Aβ)是细胞外老年斑的前体,在阿尔茨海默病(AD)患者的大脑中积累,与认知障碍和神经元细胞死亡的发生有关。Aβ由淀粉样β前体蛋白(APP)通过依次切割产生,首先由β-分泌酶切割,然后由γ-分泌酶切割。调节该途径的药物被认为是AD治疗最有前景的策略之一。在本研究中,我们发现厚朴酚显著增强SIRT3表达,减少活性氧生成和脂质过氧化,增强抗氧化活性和线粒体功能,从而降低中国仓鼠卵巢(CHO)细胞(携带淀粉样前体蛋白APP和早老素PS1突变)中的Aβ和sAPPβ水平。机制研究表明,厚朴酚既不影响APP的蛋白水平,也不影响α-分泌酶活性。相反,厚朴酚增加了AMPK、CREB和PGC-1α的表达,从而抑制β-分泌酶活性,导致Aβ水平降低。这些结果表明,厚朴酚是一种SIRT3激活剂,能够提高抗氧化活性、调节线粒体能量,同时降低Aβ水平,因此表明它是AD药物开发的先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c863/5764272/de49448bef82/pone.0190350.g001.jpg

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