Huang Hong, Liu Jiejie, Hao Haojie, Tong Chuan, Ti Dongdong, Liu Huiling, Song Haijing, Jiang Chaoguang, Fu Xiaobing, Han Weidong
Institute of Basic Medicine, Chinese PLA General Hospital, Beijing 100853, China; Medical College of Nankai University, Tianjin 300071, China.
Institute of Basic Medicine, Chinese PLA General Hospital, Beijing 100853, China.
Biomed Res Int. 2016;2016:5317630. doi: 10.1155/2016/5317630. Epub 2016 Feb 17.
To evaluate the therapeutic effects of G-CSF administration after intraosseous (IO) resuscitation in hemorrhagic shock (HS) combined with cutaneous injury rats.
The rats were randomly divided into four groups: (1) HS with resuscitation (blank), (2) HS with resuscitation + G-CSF (G-CSF, 200 μg/kg body weight, subcutaneous injection), (3) HS with resuscitation + normal saline solution injection (normal saline), and (4) HS + G-CSF injection without resuscitation (Unres/G-CSF). To estimate the treatment effects, the vital signs of alteration were first evaluated, and then wound closure rates and homing of MSCs and EPCs to the wound skins and vasculogenesis were measured. Besides, inflammation and vasculogenesis related mRNA expressions were also examined.
IO infusion hypertonic hydroxyethyl starch (HHES) exhibited beneficial volume expansion roles and G-CSF administration accelerated wound healing 3 days ahead of other groups under hemorrhagic shock. Circulating and the homing of MSCs and EPCs at wound skins were significantly elevated at 6 h after G-CSF treatment. Inflammation was declined since 3 d while angiogenesis was more obvious in G-CSF treated group on day 9.
These results suggested that the synergistical application of HHES and G-CSF has life-saving effects and is beneficial for improving wound healing in HS combined with cutaneous injury rats.
评估在失血性休克(HS)合并皮肤损伤大鼠的骨内(IO)复苏后给予粒细胞集落刺激因子(G-CSF)的治疗效果。
将大鼠随机分为四组:(1)失血性休克并复苏组(空白组),(2)失血性休克并复苏 + G-CSF组(G-CSF,200μg/kg体重,皮下注射),(3)失血性休克并复苏 + 注射生理盐水组(生理盐水组),以及(4)未复苏 + G-CSF注射组(未复苏/G-CSF组)。为评估治疗效果,首先评估生命体征的变化,然后测量伤口闭合率以及间充质干细胞(MSCs)和内皮祖细胞(EPCs)向伤口皮肤的归巢情况和血管生成情况。此外,还检测了炎症和血管生成相关的mRNA表达。
骨内输注高渗羟乙基淀粉(HHES)显示出有益的扩容作用,并且在失血性休克情况下,给予G-CSF比其他组提前3天加速了伤口愈合。G-CSF治疗后6小时,伤口皮肤处循环的MSCs和EPCs以及它们的归巢显著增加。自第3天起炎症减轻,而在第9天G-CSF治疗组的血管生成更为明显。
这些结果表明,HHES和G-CSF的协同应用具有挽救生命的作用,并且有利于改善失血性休克合并皮肤损伤大鼠的伤口愈合。