Influence of the δ-opioid receptor DADLE on serum protein S-100B after global cerebral ischemia and reperfusion in rats
- VernacularTitle:δ阿片受体激动剂DADLE对全脑缺血-再灌注大鼠血清S-100B蛋白的影响
- Author:
Jieyun HAN
;
Zijing LIANG
;
Yanqi FAN
- Publication Type:Journal Article
- Keywords:
S-opioid receptor;
Global cerebral ischemia and reperfusion;
Protein S-100B
- From:
Chinese Journal of Emergency Medicine
2008;17(6):618-621
- CountryChina
- Language:Chinese
-
Abstract:
Objective To observe the influence of δ-opioid reperfusion in rats with change in serum protein S-100B level and to explore the neuroprotective effect of DADLE during cerebral resuscitation. Method The model of global cerebral ischemia and reperfusion was induced by bilateral common carol id artery occlusion combined with hypotension. Fifty SD rats were randomly divided into five groups: sham operation group, model group, DADLE pretreated group, DADI.E treated postischemia group, DADLE treatment during reperfusion group ( n = 10 for each group) .In sham operation group,the rats were operated without ischemia and treatment; in model group, rats had global cerebral ischemia and reperfusion model up without any treament; in DADLE pretreated group, rats received DADlE before ischemia; in DADLE treatment postischemia group,rats had DADLE immediately after ischemia; in DADLE treatment during reperfusion group,rats got DADLE during early reperfusion. After the establishment of model, serum protein S-JOOB was measured by using ELlSA.One-way analysis of variance and SNK test were used for comparison between groups. Results The serum protein S-100B level was (475.56±1.93) pg/ml in sham operational group and that was much lower than that in model group and DADLE treatment groups. While the levels of serum protein S-100B in all DADLE treatment groups were reduced significantly in comparison with model group. There were no differences in the levels of serum protein KS-100B between DADLE treatment groups. Conclusions The δ-opioid receptor DADLE exerts neuroprotective effects on global cerebral ischemia and reperfusion in rats.
