Pietz K, Odin P, Funa K, Lindvall O
Restorative Neurology Unit, Department of Neurology, University Hospital, Sweden.
Neurosci Lett. 1996 Feb 2;204(1-2):101-4. doi: 10.1016/0304-3940(96)12326-0.
The effects of platelet-derived growth factor (PDGF)-AA and -BB on 6-hydroxydopamine (6-OHDA)-induced degeneration of dopaminergic (DA) neurons were studied in cultures of dissociated fetal rat mesencephalon. The 6-OHDA lesion (0.3% for 4 h) caused a selective 75% loss of tyrosine hydroxylase (TH)-positive DA neurons. The neuronal death was significantly decreased (to about 25%) by addition of 1, 10 or 30 (but not 0.1) ng/ml of PDGF-BB 24 h prior to the insult. In contrast, treatment with PDGF-AA (30 ng/ml) for 24 h before the lesion or addition of PDGF-BB (30 ng/ml) simultaneously with or 1 h after 6-OHDA did not promote the survival of TH-positive neurons. We conclude that PDGF-BB can counteract 6-OHDA-induced degeneration of mesencephalic DA neurons.
在离体培养的胎鼠中脑,研究了血小板源性生长因子(PDGF)-AA和-BB对6-羟基多巴胺(6-OHDA)诱导的多巴胺能(DA)神经元变性的影响。6-OHDA损伤(0.3%,4小时)导致酪氨酸羟化酶(TH)阳性DA神经元选择性丧失75%。在损伤前24小时加入1、10或30(而非0.1)ng/ml的PDGF-BB,可使神经元死亡显著减少(降至约25%)。相比之下,在损伤前用PDGF-AA(30 ng/ml)处理24小时,或在6-OHDA处理的同时或之后1小时加入PDGF-BB(30 ng/ml),均不能促进TH阳性神经元的存活。我们得出结论,PDGF-BB可以对抗6-OHDA诱导的中脑DA神经元变性。