Iihara K, Hashimoto N, Tsukahara T, Sakata M, Yanamoto H, Taniguchi T
Department of Neurosurgery, Maizuru Municipal Hospital, Kyoto, Japan.
J Cereb Blood Flow Metab. 1997 Oct;17(10):1097-106. doi: 10.1097/00004647-199710000-00012.
Our previous studies demonstrated coordinate expression of platelet-derived growth factor (PDGF) -B chain and beta-receptor in neurons at risk in the rat brain with focal ischemia. To clarify a role of the -B chain in the brain further, we examined whether PDGF-A or -B chain protects CA1 pyramidal neurons from delayed neuronal death after forebrain ischemia in rats. Pretreatment with PDGF-BB, but not -AA, at 120 ng/d for 2 days until forebrain ischemia was performed markedly ameliorated delayed neuronal death in CA1 pyramidal neurons on day 7 after ischemia. This neuroprotective effect of PDGF-BB was dose-dependent, and pretreatment with PDGF-BB at 240 ng/d showed almost complete inhibition of delayed neuronal death. In contrast, posttreatment with PDGF-BB at 120 ng/d starting 20 minutes after ischemia demonstrated no significant neuroprotective effect. The current study established marked neuroprotective actions of PDGF-BB in ischemic neuronal damage.
我们先前的研究表明,在局灶性缺血的大鼠脑内,处于危险中的神经元中血小板源性生长因子(PDGF)-B链和β受体呈协同表达。为进一步阐明-B链在脑内的作用,我们研究了PDGF-A或-B链是否能保护大鼠前脑缺血后CA1锥体神经元免于迟发性神经元死亡。在缺血前2天,以120 ng/d的剂量用PDGF-BB而非PDGF-AA预处理,可显著改善缺血后第7天CA1锥体神经元的迟发性神经元死亡。PDGF-BB的这种神经保护作用呈剂量依赖性,以240 ng/d的剂量用PDGF-BB预处理几乎可完全抑制迟发性神经元死亡。相比之下,在缺血后20分钟开始以120 ng/d的剂量用PDGF-BB进行后处理,未显示出明显的神经保护作用。当前研究证实了PDGF-BB在缺血性神经元损伤中具有显著的神经保护作用。