Utada Kohji, Ishida Kazuyoshi, Tohyama Suguru, Urushima Yutaka, Mizukami Yoichi, Yamashita Atsuo, Uchida Masato, Matsumoto Mishiya
Department of Anesthesiology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi, 755-8505, Japan.
J Anesth. 2015 Oct;29(5):741-8. doi: 10.1007/s00540-015-2031-y. Epub 2015 May 24.
Insulin-like growth factor 1 (IGF-1) and erythropoietin (EPO) have been reported to independently protect against ischemic spinal cord injury in rabbits. In the present study, we investigated whether the combination of IGF-1 and EPO protects against ischemic spinal cord injury in rabbits.
Animals were assigned to 1 of 4 groups (n = 6 in each): a control group (saline), an IGF-1 group (IGF-1 0.3 mg/kg), an EPO group (EPO 800 U/kg), or an IGF-1 + EPO group (IGF-1 0.3 mg/kg + EPO 800 U/kg). Spinal cord ischemia was produced by occluding the abdominal aorta for 15 min. Saline, IGF-1, and EPO were administered intravenously just after the start of reperfusion. Hindlimb motor function was assessed daily for 7 days, after which histopathological evaluation was performed. To analyze phosphorylation of signal transduction molecules, animals were assigned to 1 of the 4 groups (n = 8 in each). Spinal cord ischemia and the treatment were the same as those described above. The spinal cords were removed at 15 or 30 min after reperfusion and used to analyze phosphorylation of signal transduction molecules. Four animals served as the preischemic control, and the spinal cord was removed just before the start of ischemia.
In the IGF-1 + EPO group, both neurological and histopathological outcomes were significantly improved as compared to the control group, which was consistent with the increase of Janus kinase-2 (JAK2) phosphorylation.
The combination of IGF-1 and EPO protects against ischemic spinal cord injury in rabbits. JAK2 might contribute to the protective effect.
据报道,胰岛素样生长因子1(IGF-1)和促红细胞生成素(EPO)可独立保护兔免受缺血性脊髓损伤。在本研究中,我们调查了IGF-1和EPO联合使用是否能保护兔免受缺血性脊髓损伤。
将动物分为4组中的1组(每组n = 6):对照组(生理盐水)、IGF-1组(IGF-1 0.3 mg/kg)、EPO组(EPO 800 U/kg)或IGF-1 + EPO组(IGF-1 0.3 mg/kg + EPO 800 U/kg)。通过阻断腹主动脉15分钟来产生脊髓缺血。在再灌注开始后立即静脉注射生理盐水、IGF-1和EPO。每天评估后肢运动功能,持续7天,之后进行组织病理学评估。为了分析信号转导分子的磷酸化,将动物分为4组中的1组(每组n = 8)。脊髓缺血和治疗与上述相同。在再灌注后15或30分钟取出脊髓,用于分析信号转导分子的磷酸化。4只动物作为缺血前对照,在缺血开始前取出脊髓。
与对照组相比,IGF-1 + EPO组的神经学和组织病理学结果均显著改善,这与Janus激酶2(JAK2)磷酸化的增加一致。
IGF-1和EPO联合使用可保护兔免受缺血性脊髓损伤。JAK2可能有助于发挥保护作用。