Liu Xing-Zhen, Sun Xin, Shen Kang-Ping, Jin Wen-Jie, Fu Zhi-Yi, Tao Hai-Rong, Xu Zhi-Xing
Shanghai Key Laboratory of Orthopedic Implants, Department of Orthopedic Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Neural Regen Res. 2017 Jul;12(7):1166-1171. doi: 10.4103/1673-5374.211198.
Aldehyde dehydrogenase 2 (ALDH) is an important factor in inhibiting oxidative stress and has been shown to protect against renal ischemia/reperfusion injury. Therefore, we hypothesized that ALDH could reduce spinal cord ischemia/reperfusion injury. Spinal cord ischemia/reperfusion injury was induced in rats using the modified Zivin's method of clamping the abdominal aorta. After successful model establishment, the agonist group was administered a daily consumption of 2.5% alcohol. At 7 days post-surgery, the Basso, Beattie, and Bresnahan score significantly increased in the agonist group compared with the spinal cord ischemia/reperfusion injury group. ALDH expression also significantly increased and the number of apoptotic cells significantly decreased in the agonist group than in the spinal cord ischemia/reperfusion injury group. Correlation analysis revealed that ALDH expression negatively correlated with the percentage of TUNEL-positive cells ( = -0.485, < 0.01). In summary, increased ALDH expression protected the rat spinal cord against ischemia/reperfusion injury by inhibiting apoptosis.
乙醛脱氢酶2(ALDH)是抑制氧化应激的一个重要因素,并且已被证明可预防肾缺血/再灌注损伤。因此,我们推测ALDH可减轻脊髓缺血/再灌注损伤。采用改良的齐文夹闭腹主动脉法在大鼠中诱导脊髓缺血/再灌注损伤。成功建立模型后,激动剂组每日给予2.5%酒精。术后7天,与脊髓缺血/再灌注损伤组相比,激动剂组的巴索、贝蒂和布雷斯纳汉评分显著升高。激动剂组的ALDH表达也显著增加,且凋亡细胞数量比脊髓缺血/再灌注损伤组显著减少。相关性分析显示,ALDH表达与TUNEL阳性细胞百分比呈负相关(r = -0.485,P < 0.01)。总之,ALDH表达增加通过抑制凋亡保护大鼠脊髓免受缺血/再灌注损伤。