Aldehyde dehydrogenase 2 overexpression inhibits neuronal apoptosis after spinal cord ischemia/reperfusion injury

被引:21
作者
Liu, Xing-zhen [1 ]
Sun, Xin [1 ]
Shen, Kang-ping [1 ]
Jin, Wen-jie [1 ]
Fu, Zhi-yi [1 ]
Tao, Hai-rong [1 ]
Xu, Zhi-xing [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Orthoped Surg,Shanghai Key Lab Orthoped Impl, Shanghai, Peoples R China
关键词
nerve regeneration; spinal cord ischemia/reperfusion injury; aldehyde dehydrogenase 2; alcohol; apoptosis; oxidative stress; terminal deoxynucleotidyl transferase dUTP nick-end labeling; neural regeneration; ISCHEMIA-REPERFUSION INJURY; MYOCARDIAL ISCHAEMIA/REPERFUSION INJURY; ACTIVATED PROTEIN-KINASE; OXIDATIVE STRESS; RENAL ISCHEMIA; PATHWAY; INFARCTION; AUTOPHAGY; RAT; CARDIOMYOCYTES;
D O I
10.4103/1673-5374.211198
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aldehyde dehydrogenase 2 (ALDH2) is an important factor in inhibiting oxidative stress and has been shown to protect against renal ischemia/reperfusion injury. Therefore, we hypothesized that ALDH2 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. ALDH2 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 ALDH2 expression negatively correlated with the percentage of TUNEL-positive cells (r = -0.485, P < 0.01). In summary, increased ALDH 2 expression protected the rat spinal cord against ischemia/reperfusion injury by inhibiting apoptosis.
引用
收藏
页码:1166 / 1171
页数:6
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