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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.
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页码:1166 / 1171
页数:6
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