Hasegawa Hiroshi, Takano Hiroyuki, Iwanaga Koji, Ohtsuka Masashi, Qin Yingjie, Niitsuma Yuriko, Ueda Kazutaka, Toyoda Tomohiko, Tadokoro Hiroyuki, Komuro Issei
Department of Cardiovascular Science and Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
J Am Coll Cardiol. 2006 Feb 21;47(4):842-9. doi: 10.1016/j.jacc.2005.09.048. Epub 2006 Jan 26.
The aim of this study was to investigate the effect of granulocyte colony-stimulating factor (G-CSF) on chronic myocardial ischemia in swine.
We recently have reported that G-CSF prevents cardiac remodeling and dysfunction after acute myocardial infarction in mice and swine. It remains unclear whether G-CSF has beneficial effects on chronic myocardial ischemia.
An ameroid constrictor was placed on left circumflex coronary artery of swine. The presence of myocardial ischemia was verified at four weeks after the operation, and the animals were randomly assigned into the following two groups: 1) administration of vehicle (control group, n = 10), and 2) administration of G-CSF (10 microg/kg/day) for seven days (G-CSF group, n = 10).
Echocardiographic examination revealed that the G-CSF treatment prevented left ventricular dilation and dysfunction at eight weeks after the operation. Stress echocardiography revealed that G-CSF ameliorated the regional contractility of chronic myocardial ischemia. Morphological analysis revealed that the extent of myocardial fibrosis of the ischemic region was less in the G-CSF group than in control group. There were more vessels and less apoptotic cells at the ischemic region of the heart of the G-CSF group than control group. Moreover, Akt1 was more strongly activated in the heart of the G-CSF group than control group.
These findings suggest that G-CSF improves cardiac function of chronic myocardial ischemia through decreases in fibrosis and apoptotic death and an increase in vascular density in the ischemic region.
本研究旨在探讨粒细胞集落刺激因子(G-CSF)对猪慢性心肌缺血的影响。
我们最近报道,G-CSF可预防小鼠和猪急性心肌梗死后的心脏重塑和功能障碍。G-CSF对慢性心肌缺血是否具有有益作用仍不清楚。
在猪的左旋冠状动脉上放置一个阿梅氏缩窄器。术后四周证实存在心肌缺血,将动物随机分为以下两组:1)给予赋形剂(对照组,n = 10),2)给予G-CSF(10微克/千克/天),持续7天(G-CSF组,n = 10)。
超声心动图检查显示,G-CSF治疗可预防术后8周左心室扩张和功能障碍。负荷超声心动图显示,G-CSF改善了慢性心肌缺血的局部收缩性。形态学分析显示,G-CSF组缺血区域的心肌纤维化程度低于对照组。G-CSF组心脏缺血区域的血管比对照组多,凋亡细胞比对照组少。此外,G-CSF组心脏中Akt1的激活程度比对照组更强。
这些发现表明,G-CSF通过减少纤维化和凋亡死亡以及增加缺血区域的血管密度来改善慢性心肌缺血的心脏功能。