Date Ichiro, Takagi Norio, Takagi Keiko, Kago Tomoyuki, Matsumoto Kunio, Nakamura Toshikazu, Takeo Satoshi
Department of Pharmacology, Tokyo University of Pharmacy and Life Science, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392 Tokyo, Japan.
J Neurosci Res. 2004 Nov 1;78(3):442-53. doi: 10.1002/jnr.20263.
Hepatocyte growth factor (HGF), an organotropic factor for regeneration and protection in various organs, has the ability to attenuate cerebral ischemia-induced cell death. The effect of HGF on learning and memory function after cerebral ischemia, however, remains unknown. We have demonstrated that administration of human recombinant HGF (hrHGF) into the ventricle reduced prolongation of the escape latency in acquisition and retention tests of the water maze task on Days 12-28 after microsphere embolism-induced cerebral ischemia. Treatment with hrHGF also attenuated the decrease in viable area and the density and number of perfused cerebral vessels, particularly those with a diameter smaller than 10 microm, of the ipsilateral hemisphere on Day 28 after the cerebral ischemia. We observed that treatment with hrHGF reduced the number of TUNEL-positive cerebral endothelial cells at the early stage after the ischemia. These results suggest that hrHGF prevents learning and memory dysfunction seen after sustained cerebral ischemia by protecting against injury to the endothelial cells. HGF treatment may be a potent therapeutic strategy for cerebrovascular diseases, including cerebral infarct and vascular dementia.
肝细胞生长因子(HGF)是一种促进多种器官再生和保护的器官营养因子,具有减轻脑缺血诱导的细胞死亡的能力。然而,HGF对脑缺血后学习和记忆功能的影响仍不清楚。我们已经证明,在微球栓塞诱导的脑缺血后第12至28天,向脑室内注射人重组HGF(hrHGF)可减少水迷宫任务的获取和保持测试中逃避潜伏期的延长。hrHGF治疗还可减轻脑缺血后第28天同侧半球存活面积以及灌注脑血管的密度和数量的减少,尤其是直径小于10微米的血管。我们观察到,hrHGF治疗可减少缺血后早期TUNEL阳性脑内皮细胞的数量。这些结果表明,hrHGF通过保护内皮细胞免受损伤,预防持续性脑缺血后出现的学习和记忆功能障碍。HGF治疗可能是包括脑梗死和血管性痴呆在内的脑血管疾病的有效治疗策略。