Frodl E M, Nakao N, Brundin P
Department of Neurology, University Hospital of Lund, Sweden.
Neuroreport. 1994 Nov 21;5(17):2393-6. doi: 10.1097/00001756-199411000-00045.
We have studied the effects of two lazaroids, U-74389G and U-83836E, on the survival of cultured rat dopamine neurones. Lazaroids are inhibitors of free radical formation and lipid peroxidation. Dissociated embryonic mesencephalic neurones were cultivated for 2 or 7 days under serum-free conditions with or without the addition of 0.3 microM of one of the lazaroids. Both lazaroids enhanced the survival of tyrosine hydroxylase immunoreactive, dopaminergic neurones both after 2 and 7 days in vitro to around 111-120% and 175-180% of controls, respectively. Since the total number of neurones was also increased following lazaroid treatment, it is unlikely that lazaroids exert their effects on only dopamine neurones. These findings suggest that oxidative stress plays an important role in the death of cultured embryonic dopamine neurones and that lazaroids may be potent neuroprotective agents in situations where dopaminergic neurones degenerate.
我们研究了两种拉扎oids(U-74389G和U-83836E)对培养的大鼠多巴胺神经元存活的影响。拉扎oids是自由基形成和脂质过氧化的抑制剂。将解离的胚胎中脑神经元在无血清条件下培养2天或7天,添加或不添加0.3微摩尔的其中一种拉扎oids。两种拉扎oids在体外培养2天和7天后,均提高了酪氨酸羟化酶免疫反应性多巴胺能神经元的存活率,分别达到对照组的约111-120%和175-180%。由于拉扎oid处理后神经元总数也增加了,因此拉扎oids不太可能仅对多巴胺神经元发挥作用。这些发现表明,氧化应激在培养的胚胎多巴胺神经元死亡中起重要作用,并且拉扎oids在多巴胺能神经元退化的情况下可能是有效的神经保护剂。