Cheng Yue-Fa, Zhu Guoqi, Wu Qing-Wen, Xie Yue-Sheng, Jiang Yan, Guo Lan, Guan Ya-Li, Liu Ying-Shuo, Zhang Jun
Jitang College of North China University of Science and Technology, Tangshan, 063000, China.
Key Laboratory of Xin'an Medicine, Ministry of Education, Anhui University of Chinese Medicine, Hefei, 230038, China.
J Mol Neurosci. 2017 Feb;61(2):227-234. doi: 10.1007/s12031-016-0856-y. Epub 2016 Oct 30.
The neuroprotective action of puerarin in Parkinson's disease (PD) models has been well investigated. However, the mechanisms involved in protection have not been completely understood. G protein-coupled receptor 30 (GPR30) is a G protein-coupled estrogen receptor and considered a potential target in the neuroprotection against PD. In this study, we investigated whether puerarin prevented against 1-methyl-4-phenylpyridinium (MPP)-induced cell death via GPR30. Our results showed that the GPR30 agonist, G1, exhibited puerarin-mediated neuroprotection against MPP-induced cell death of SH-SY5Y cells. This protective action was reversed by the GPR30 antagonist. Moreover, a time- and concentration-dependent effect of puerarin on GPR30 expression was verified at the protein level but not at the mRNA level. Further, we showed that an mTor-dependent new GPR30 synthesis contributed to the protection conferred by puerarin. Finally, glial cell line-derived neurotrophic factor (GDNF) levels were enhanced by puerarin and G1 in both control and MPP-lesioned cells via GPR30. Taken together, our data strongly suggest that puerarin prevents MPP-induced cell death via facilitating GPR30 expression and GDNF release.
葛根素在帕金森病(PD)模型中的神经保护作用已得到充分研究。然而,其保护机制尚未完全明确。G蛋白偶联受体30(GPR30)是一种G蛋白偶联雌激素受体,被认为是抗PD神经保护的潜在靶点。在本研究中,我们探究了葛根素是否通过GPR30预防1-甲基-4-苯基吡啶离子(MPP)诱导的细胞死亡。我们的结果表明,GPR30激动剂G1表现出葛根素介导的对MPP诱导的SH-SY5Y细胞死亡的神经保护作用。这种保护作用被GPR30拮抗剂逆转。此外,在蛋白质水平而非mRNA水平验证了葛根素对GPR30表达的时间和浓度依赖性效应。进一步地,我们表明mTor依赖性的新GPR30合成有助于葛根素赋予的保护作用。最后,在对照细胞和MPP损伤细胞中,葛根素和G1均通过GPR30提高了胶质细胞源性神经营养因子(GDNF)水平。综上所述,我们的数据强烈表明葛根素通过促进GPR30表达和GDNF释放来预防MPP诱导的细胞死亡。