Research Center for Neuroscience, Institute of Molecular Biosciences, Mahidol University, Salaya, Nakhonpathom, 73170, Thailand.
Department of Companion Animal Clinical Sciences, Faculty of Veterinary Medicine, Kasetsart University, Kamphaeng Saen, Nakhonpathom, 73140, Thailand.
Drug Chem Toxicol. 2022 Jan;45(1):44-51. doi: 10.1080/01480545.2019.1658768. Epub 2019 Sep 9.
Oxidative stress is implicated in pathogenesis of neurodegenerative disorders, such as Alzheimer's and Parkinson's diseases. The study demonstrates diarylpropionitrile (DPN), an antioxidant selective agonist of estrogen receptor β, protected human neuroblastoma SH-SY5Y cells against HO-induced toxicity by attenuating production of reactive oxygen species, apoptosis, autophagy, NF-κB activation, MAPK p38, JNK and ERK 1/2 signaling pathways, and β-site amyloid precursor protein cleaving enzyme level, but, interestingly, stimulating Akt pathway. These findings indicate the important potential of DPN to ameliorate oxidative stress-associated damage in neurodegenerative disorders.
氧化应激与神经退行性疾病(如阿尔茨海默病和帕金森病)的发病机制有关。本研究表明,二芳基丙腈(DPN),一种雌激素受体β的抗氧化选择性激动剂,通过减轻活性氧的产生、细胞凋亡、自噬、NF-κB 激活、MAPK p38、JNK 和 ERK1/2 信号通路以及β-位点淀粉样前体蛋白裂解酶水平,来保护人神经母细胞瘤 SH-SY5Y 细胞免受 HO 诱导的毒性,但有趣的是,它还能刺激 Akt 通路。这些发现表明 DPN 具有改善神经退行性疾病中与氧化应激相关的损伤的重要潜力。