Singh Shalini, Ahmad Riyaz, Mathur Deepti, Sagar Ravinder Kumar, Krishana Bal
Department of Physiology, Maulana Azad Medical College, New Delhi, India.
Indian J Exp Biol. 2006 Sep;44(9):699-704.
Brain derived neurotrophic factor (BDNF) has been shown to exert trophic effects on dopaminergic neurons against 6-hydroxydopamine (6-OHDA) in young rat. Since the degeneration of substantia nigra dopaminergic neurons that occurs in Parkinson's disease is more often than not confined to elderly individuals, it is of interest to determine whether the effects of BDNF against 6 hydroxydopamine (6-OHDA) in young rats can be extended to aged animals. 6-hydroxydopamine was stereotaxically injected into the striatum of young (3-months) and aged (24-months) rats, which were treated two hours earlier with BDNF. 6-OHDA results in almost complete destruction of substantia nigra pars compacta dopaminergic neurons. BDNF injection significantly changed apomorphine induced rotations from 132 +/- 15 to 181 +/- 10, staircase test from 73 +/- 2% to 61 +/- 3%, initiation time from 7 +/- 2 to 12 +/- 1 sec, and disengage time from 80 +/- 7 to 90 +/- 5 sec in young and aged animals, respectively. It is concluded that BDNF causes the limited behavior recovery of striatal DA systems from 6-OHDA toxicity in aged animals.
脑源性神经营养因子(BDNF)已被证明对幼鼠的多巴胺能神经元具有营养作用,可对抗6-羟基多巴胺(6-OHDA)。由于帕金森病中发生的黑质多巴胺能神经元变性通常局限于老年人,因此确定BDNF在幼鼠中对抗6-羟基多巴胺(6-OHDA)的作用是否能扩展到老年动物是很有意义的。将6-羟基多巴胺立体定向注射到幼龄(3个月)和老龄(24个月)大鼠的纹状体中,这些大鼠在两小时前用BDNF进行了处理。6-OHDA几乎完全破坏了黑质致密部的多巴胺能神经元。在幼龄和老龄动物中,注射BDNF分别使阿扑吗啡诱导的旋转从132±15次显著变为181±10次,阶梯试验从73±2%变为61±3%,起始时间从7±2秒变为12±1秒,脱离时间从80±7秒变为90±5秒。结论是,BDNF可使老年动物纹状体DA系统从6-OHDA毒性中有限地恢复行为。