Protection against MPTP treatment by an analog of Pro-Leu-Gly-NH2 (PLG, MIF-1)

被引:26
作者
Marcotte, ER
Chugh, A
Mishra, RK
Johnson, RL
机构
[1] McMaster Univ, Dept Psychiat, Fac Hlth Sci, Hamilton, ON L8N 3Z5, Canada
[2] Univ Minnesota, Dept Med Chem, Minneapolis, MN 55455 USA
[3] McMaster Univ, Dept Biomed Sci, Fac Hlth Sci, Hamilton, ON L8N 3Z5, Canada
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0196-9781(97)00321-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
3(R)-[(2(S)-Pyrrolidinylcarbonyl)amino]-2-oxo-1-pyrrolidineacetamide (PAOPA) is a peptidomimetic analog of Pro-Leu-Gly-NH2 (PLG or MLF-1) that has previously been demonstrated to be more potent and efficacious that MLF-1 in enhancing dopamine receptor activity. Given the ability of MIF-1 to protect against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) lesioning in C57 BL/6 mice, the present study was undertaken to evaluate the neuroprotective effect of PAOPA in this model. PAOPA was found to be more potent and efficacious that MIF-1 in sparing dopamine and its metabolite levels following 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine administration. Whether the enhanced neuroprotective effect of PAOPA is due to dopamine receptor stimulation, or a result of reduced oxidative stress through normalization of dopamine turnover, remains to be determined. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:403 / 406
页数:4
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