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

Aldehyde dehydrogenase 2 (ALDH(2)) is an important factor in inhibiting oxidative stress and has been shown to protect against renal ischemia/reperfusion injury. Therefore, we hypothesized that ALDH(2) could reduce spinal cord ischemia/reperfusion injury. Spinal cord ischemia/reperfusion injury was...

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Detalles Bibliográficos
Autores principales: Liu, Xing-zhen, Sun, Xin, Shen, Kang-ping, Jin, Wen-jie, Fu, Zhi-yi, Tao, Hai-rong, Xu, Zhi-xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558498/
https://www.ncbi.nlm.nih.gov/pubmed/28852401
http://dx.doi.org/10.4103/1673-5374.211198
Descripción
Sumario:Aldehyde dehydrogenase 2 (ALDH(2)) is an important factor in inhibiting oxidative stress and has been shown to protect against renal ischemia/reperfusion injury. Therefore, we hypothesized that ALDH(2) 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(2) 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(2) 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.