کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4339011 1614896 2011 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
BL-1023 improves behavior and neuronal survival in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-intoxicated mice
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
BL-1023 improves behavior and neuronal survival in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-intoxicated mice
چکیده انگلیسی

The therapeutic potential of BL-1023, a chemical combination of l-3,4-dihydroxyphenylalanine (l-DOPA) and gamma-aminobutyric acid (GABA), was investigated in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) intoxicated mice. Such animals exhibit nigrostriatal degeneration, characteristic of human Parkinson's disease. Drug was administered during and after the development of MPTP-induced nigrostriatal lesions followed by measures of motor function and behavior, surviving nigrostriatal dopaminergic neurons and termini, and striatal dopamine levels. When administered after lesion development, BL-1023 improved motor function of MPTP-mice as measured by rotarod, total floor and vertical plane movements, and stereotypic movements in open field activity tests compared to MPTP-mice without treatment. This also paralleled modest nigral dopaminergic neuronal protection. Such significant improvements in motor function, behaviors, and dopaminergic neuronal numbers were not seen when BL-1023 was administered during MPTP-induced lesion development. The data demonstrate select abilities of BL-1023 to increase dopaminergic neuronal survival and improve motor function in MPTP-mice.

▶BL-1023 is a combination of l-3,4-dihydroxyphenylalanine (L-DOPA) and gamma-aminobutyric acid (GABA). ▶BL-1023 is a potential Parkinson's disease therapeutic. ▶We investigated the therapeutic potential of BL-1023 in MPTP-intoxicated mice. ▶BL-1023 increases motor function, activity, and neuronal survival in MPTP mice.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 180, 28 April 2011, Pages 293–304
نویسندگان
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