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作 者:郭立军[1,2] 江高峰[3] 李海鹏[1] 李琼[1] 刘恩岐[4] 李洁[1,3]
机构地区:[1]南华大学附属郴州市第一人民医院,湖南郴州423000 [2]湘南学院,湖南郴州423000 [3]南华大学药物药理研究所,湖南衡阳421001 [4]西安交通大学医学院实验动物中心,陕西西安710061
出 处:《中国药理学通报》2015年第6期827-833,共7页Chinese Pharmacological Bulletin
基 金:国家自然科学基金资助项目(No 81202535);郴州市科技局资助项目(No CZ2014015)
摘 要:目的探讨mm LDL对小鼠肠系膜动脉α1受体的作用。方法小鼠尾静脉注射mm LDL,微血管肌张力描记仪观察NA引起的小鼠肠系膜动脉收缩量效曲线变化,RTPCR、Western blot检测α1受体及α2受体表达。结果mm LDL引起NA收缩量效曲线明显增强,表现为Emax值由生理盐水(NS)组的(120.75±3.44)%上升为(161.00±6.87)%(P<0.01),p EC50值由NS组的(5.65±0.05)上升为(6.20±0.08)(P<0.01)。α1受体拮抗剂哌唑嗪引起量效曲线的明显右移,mm LDL引起α1受体m RNA水平、蛋白表达明显增加,对α2受体表达基本没有影响。结论尾静脉注射mm LDL上调小鼠肠系膜动脉α1受体。Aim To investigate the effects of mmLDL on the up-regulation ofα1 receptors in moues mesenteric arteries. Methods Mice tail intravenous injection of mmLDL was used . Vitro sensitive myograph was employed to examine Noradrenaline ( NA) induced vascular contraction on mice mesenteric artery, and the mRNA and protein expressions ofα1 andα2 receptors were an-alyzed by real-time PCR and Western blot, respective-ly. Results mmLDL significantly increased NA in-duced concentration-contractile curve, and the data of Emax and pEC50 were from ( 122. 61 ± 9. 40 )% and (5. 65 ± 0. 05 ) in normal saline ( NS ) group to (161. 01 ± 6. 90 )% and ( 6. 20 ± 0. 08 ) in mmLDL group (P 〈0. 01, P 〈0. 01), respectively. The α1 adrenoceptor antagonist prazosin shifted the concentration-contractile curve induced by NA towards right. Af-ter using mmLDL, the mRNA and protein levels of α1 adrenoceptor were significantly increased, but the mR-NA and protein levels of α2 adrenoceptor were not changed. Conclusion Tail intravenous injection of mmLDL enhances the vascular expressions of α1 adre-noceptors and the contractile effects mediated byα1 ad-renoceptors.
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