Protective effect of adenosine preconditioning against spinal cord ischemia-reperfusion injury in rats.
- Author:
Qi FU
1
;
Zhengfang ZHOU
;
Xiaohui LI
;
Huiming GUO
;
Xiaoping FAN
;
Jimei CHEN
;
Jian ZHUANG
;
Shaoyi ZHENG
;
Ping ZHU
Author Information
- Publication Type:Journal Article
- MeSH: Adenosine; pharmacology; Animals; Apoptosis; drug effects; Caspase 12; metabolism; Heat-Shock Proteins; metabolism; Ischemic Preconditioning; methods; Male; Rats; Rats, Sprague-Dawley; Reperfusion Injury; metabolism; Spinal Cord Ischemia; metabolism
- From: Journal of Southern Medical University 2014;34(1):92-95
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the effect of adenosine preconditioning on cell apoptosis and expressions of glucose-regulated protein (GRP-78) and cysteinyl aspartate-specific protease 12 (caspase-12) in rats with spinal cord ischemia-reperfusion injury.
METHODSTwenty-seven rats were randomized into 3 equal groups and subjected to sham operation (group A), spinal cord ischemia-reperfusion injury (group B), or ischemia-reperfusion injury with adenosine treatment. Spinal cord ischemia-reperfusion injury was induced by cross-clamping of the abdominal aorta inferior to the left renal artery. The spinal cord function was assessed using the Modified Tarlov Scale at 6, 12, and 24 h after reperfusion. At 24 h after reperfusion, histological analysis was carried out with HE staining; cell apoptosis and viability were determined with TUNEL staining, and the expressions of GRP-78 and caspase-12 proteins were determined with Western blotting.
RESULTSHE staining of the spinal cord showed extensive spinal cord injury such as cell edema in group B as compared with group C. Compared with group A, group B showed a significantly increased number of apoptotic cells; the number of apoptotic cells in group B was greater than that in group C. Compared with group B, group C showed significantly increased GRP-78 expression (P<0.01) and decreased caspase-12 expression (P<0.01).
CONCLUSIONAdenosine can up-regulate GRP-78 expression and down-regulate caspase-12 expression, and protects the spinal cord against ischemia-reperfusion injury by inhibiting cell apoptosis.