
浏览全部资源
扫码关注微信
重庆医科大学附属第一医院麻醉科
纸质出版日期:2011,
网络出版日期:2011-12-30,
移动端阅览
曾小华, 刘丹彦, 安民. 胞二磷胆碱预处理对大鼠脊髓缺血再灌注损伤的影响[J]. 陆军军医大学学报, 2011,33(24):2587-2591.
ZENG XIAOHUA, LIU DANYAN, AN MIN. Citicoline pretreatment protects rats against spinal cord ischemia-reperfusion injury. [J]. Journal of army medical university, 2011, 33(24): 2587-2591.
目的 探讨胞二磷胆碱对脊髓缺血再灌注损伤的影响及其作用机制。 方法 雄性SD大鼠72只,体质量(230±20)g,按随机数字表法分为3组(
n
=24):假手术组,缺血再灌注损伤组(IR组)和胞二磷胆碱预先给药组(citi组),各组按灌注后12、24、48、72 h分成4个亚组(
n
=6)。各组均采用改良Zivin法建立脊髓缺血再灌注损伤模型,并于灌注后12、24、48、72 h 4个时点采用改良Tarlov法对大鼠脊髓运动和感觉功能进行评分,HE染色观察脊髓L
2
~L
5
节段的病理学改变,TUNEL法检测脊髓凋亡细胞数,于再灌注后72 h处采用免疫组化方法检测脊髓神经元Bcl-2、Bax、caspase-9表达及Bcl-2与Bax的比值(Bcl-2/Bax)。 结果 与假手术组相比,IR组和citi组运动和感觉评分均降低,HE染色有明显的病理损伤,TUNEL染色神经细胞凋亡数量增加,免疫组化显示caspase-9 、Bcl-2、Bax蛋白表达增加,Bcl-2/Bax降低(
P
<
0.01);与IR组相比,citi组运动和感觉评分高,HE染色形态学损伤较轻,TUNEL染色神经细胞凋亡数量少,免疫组化Bcl-2表达明显增加,Bax、caspase-9表达降低,Bcl-2/Bax升高(
P
<
0.01)。 结论 胞二磷胆碱可减轻大鼠脊髓缺血再灌注损伤,改善神经功能,其机制可能与其上调Bcl-2蛋白表达,下调Bax、caspase-9蛋白表达,从而减轻神经元凋亡有关。
Objective To determine the effects of citicoline pretreatment on spinal cord ischemia-reperfusion (IR) injury in rats. Methods Seventy-two male SD rats weighing 210 to 250 g were randomly divided into 3 groups (
n
=24): sham operation group
ischemia-reperfusion injury group (group IR) and citicoline pretreatment group
(group citi). Every group was divided into 4 subgroups according to the time after reperfusion for 12
24
48 and 72 h respectively (
n
=6). After modified Zivin methods was used to establish model
Tarlov with modification was used for neurological function scores at the above mentioned time points
HE staining was employed for L
2-5
spinal cord pathological changes
TUNEL method for calculation apoptosis cells
and immunohistochemical assay for Bcl-2
Bax
caspase-9 expression. The ratio of Bcl-2 to Bax (Bcl-2/Bax) was calculated. Results Compared to Sham group
group IR and group citi showed significantly lower neurological function scores
obvious pathological injury
increased apoptotic nerve cells
enhanced expression of caspase-9
Bax and Bcl-2
and significantly lower Bcl-2/Bax ratio(
P
<
0.01). However
citi pretreatment resulted in better outcomes in above items compared to group IR(
P
<
0.01). Conclusion Citicoline pretreatment attenuates spinal cord IR injury
improves neurological function through up-regulating Bcl-2
down-regulating Bax and caspase-9
and thus reducing neuronal apoptosis.
脊髓胞二磷胆碱预处理缺血再灌注损伤凋亡
spinal cordciticolinepretreatmentischemia-reperfusionapoptosis
0
浏览量
0
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621