| Literature DB >> 27228307 |
Baek-Soo Han1, Kyoung-Shim Kim2, Yu Jin Kim3, Hoe-Yune Jung1, Young-Mi Kang2, Kyu-Suk Lee1, Mi-Jin Sohn3, Chun-Hyung Kim4,5, Kwang-Soo Kim4, Won-Gon Kim3.
Abstract
Nurr1 is an orphan nuclear receptor that is essential for the differentiation and maintenance of dopaminergic neurons in the brain, and it is a therapeutic target for Parkinson's disease (PD). During the screening for Nurr1 activators from natural sources using cell-based assay systems, a methanol extract of the combined stems and roots of Daphne genkwa was found to activate the transcriptional function of Nurr1 at a concentration of 3 μg/mL. The active components were isolated and identified as genkwanine N (1) and yuanhuacin (2). Both compounds 1 and 2 significantly enhanced the function of Nurr1 at 0.3 μM. Nurr1-specific siRNA abolished the activity of 1 and 2, strongly suggesting that transcriptional activation by 1 and 2 occurred through the modulation of Nurr1 function. Additionally, treatment with 1 and 2 inhibited 6-hydroxydopamine (6-OHDA)-induced neuronal cell death and lipopolysaccharide (LPS)-induced neuroinflammation. Moreover, in a 6-OHDA-lesioned rat model of PD, intraperitoneal administration of 2 (0.5 mg/kg/day) for 2 weeks significantly improved behavioral deficits and reduced tyrosine hydroxylase (TH)-positive dopaminergic neuron death induced by 6-OHDA injection and had a beneficial effect on the inflammatory response in the brain. Accordingly, compounds 1 and 2, the first reported Nurr1 activators of natural origin, are potential lead compounds for the treatment of PD.Entities:
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Year: 2016 PMID: 27228307 PMCID: PMC5635821 DOI: 10.1021/acs.jnatprod.6b00110
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050