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作 者:迟淑梅 王泽民[2] 张利 章晓英[1] 陈洁芳 孙保亮[3] CHI Shumei;WANG Zemin;ZHANG Li;ZHANG Xiaoying;CHEN Jiefang;SUN Baohang(Hangzhou Seventh People's Hospital, a.Department of Neurology;Department of Pharmacy, Hangzhou 310013, China;Key Lab of Cerebral Mierocirculation in Universities of Shandong, Department of Neurology, Affiliated Hospital of Taishan Medical College, Tai 'an 271000, China)
机构地区:[1]杭州市第七人民医院神经内科,杭州310013 [2]杭州市第七人民医院药剂科,杭州310013 [3]山东省高校脑微循环重点实验室泰山医学院附属医院神经内科,山东泰安271000
出 处:《中国现代应用药学》2018年第6期793-796,共4页Chinese Journal of Modern Applied Pharmacy
基 金:国家自然科学基金项目(30770759)
摘 要:目的探讨经鼻靶向中枢给予降钙素基因相关肽(calcitonin gene-related peptide,CGRP)对海马细胞凋亡和脑损伤的作用。方法枕大池2次注血法制作蛛网膜下腔出血(subarach-noid hemorrhage,SAH)模型。将48只♂Wistar大鼠随机分为正常对照组、SAH组、生理盐水(NS)+SAH组(经鼻给予NS)、CGRP+SAH组(经鼻给予CGRP),每组12只。于第2次注血3 d后,采用免疫荧光技术检测海马组织中Bcl-2和caspase-3的蛋白表达。结果免疫荧光染色显示Bcl-2和caspase-3在正常对照组大鼠海马组织中只观察到极少量表达;SAH组、NS+SAH组Bcl-2和caspase-3蛋白表达明显增多;与SAH组和NS+SAH组相比较,经鼻给予CGRP治疗后,Bcl-2表达显著升高,caspase-3表达水平显著降低,差异均具有统计学意义(P<0.01)。结论 CGRP经鼻靶向中枢给药能有效抑制SAH大鼠海马组织细胞凋亡,对脑损伤具有显著保护作用。OBJECTIVE To investigate the effect of intranasal calcitonin gene-related peptide(CGRP) on hippocampal apoptosis and cerebral injury. METHODS Subarach-noid hemorrhage(SAH) model was established by cisterna double injection of fresh autologous arterial blood. Forty-eight male Wistar rats were randomly divided into normal control group, SAH group, normal saline(NS)+SAH group(intranasal NS) and CGRP+SAH group(intranasal CGRP)(n=12). The expression of Bcl-2 and caspase-3 in hippocampal tissues was detected by immunofluorescence technique on the 3 rd day after the second injection. RESULTS Immunofluorescence staining results showed that the Bcl-2, caspase-3 expressed very small amounts in normal control group, it was obviously increased in SAH and NS+SAH group. Compared with SAH and NS+SAH group, intransal CGRP could significantly rise the expression of Bcl-2(P〈0.01) and decrease the expression of caspase-3 level significantly(P〈0.01). CONCLUSION Intransal CGRP can inhibit the apoptosis of hippocampal tissue cells effectively and have a significant protective effect on brain injury in SAH rats.
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