Antiparkinsonian Properties of a Nerve Growth Factor Dipeptide Mimetic GK-2 in in Vivo Experiments

被引:12
|
作者
Povarnina, P. Yu. [1 ]
Gudasheva, T. A. [1 ]
Vorontsova, O. N. [1 ]
Bondarenko, N. A. [1 ]
Seredenin, S. B. [1 ]
机构
[1] Russian Acad Med Sci, VV Zakusov Inst Pharmacol, Moscow, Russia
关键词
antiparkinsonian activity; low-molecular-weight dipeptide mimetic of nerve growth factor GK-2; 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine; 6-hydroxydopamine; haloperidol; DEFICITS; AGONIST; RESCUE;
D O I
10.1007/s10517-011-1417-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
An intraperitoneal injection of GK-2 (dipeptide mimetic of nerve growth factor, 0.01-5.00 mg/kg) 24 h before the adverse exposure reduced the severity of haloperidol-induced catalepsy in rats. This agent retained the activity after oral administration in a dose of 10 mg/kg. An intraperitoneal injection of GK-2 in a dose of 1 mg/kg reduced the severity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonian syndrome in mice. Administration of GK-2 45 min after haloperidol treatment was also followed by a decrease in the degree of catalepsy. The repeated intraperitoneal treatment with GK-2 in a dose of 1 mg/kg after intrastriatal injection of 6-hydroxydopamine was shown to prevent the development of apomorphine-induced rotations in rats.
引用
收藏
页码:690 / 693
页数:4
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