MPTP公司
神经毒性
多巴胺能
帕金森病
药理学
转录因子
疾病
三萜类
基因
神经科学
医学
生物
多巴胺
遗传学
传统医学
毒性
内科学
作者
Navneet Ammal Kaidery,Rebecca Banerjee,Lichuan Yang,N. A. Smirnova,Dmitry M. Hushpulian,Karen T. Liby,Charlotte R. Williams,Masayuki Yamamoto,Thomas W. Kensler,Rajiv R. Ratan,Michael B. Sporn,M. Flint Beal,Irina G. Gazaryan,Bobby Thomas
标识
DOI:10.1089/ars.2011.4491
摘要
Our results indicate that activation of Nrf2/antioxidant response element (ARE) signaling by synthetic TP is directly associated with their neuroprotective effects against MPTP neurotoxicity and suggest that targeting the Nrf2/ARE pathway is a promising approach for therapeutic intervention in PD.
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