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尾加压素受体GPR14在大鼠心血管系统及脑内的表达 被引量:3

Expression of urotensinⅡreceptor GPR14 in cardiovasculature and brain of rats
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摘要 目的 :观察尾加压素 (U )受体 GPR14在 SD大鼠心血管系统及脑内的表达。 方法 :采用半定量逆转录 -聚合酶链反应 (RT- PCR)检测 GPR14。 结果 :在心血管系统中 ,大鼠颈总动脉、胸主动脉、左心房及左心室均表达 GPR14m RNA,其中心室表达丰度最高 ;在中枢神经系统中 ,大鼠小脑、大脑皮质、下丘脑及海马均表达 GPR14m RNA,其中小脑表达丰度较高。结论 :U 受体 GPR14在大鼠心血管系统及脑组织中都有表达 ,提示 U 在心血管及中枢神经活动中发挥重要作用。 Objective: To observe the expression of the G-protein-coupled-receptor 14 (GPR14), urotensinⅡreceptor, in the cardiovascular system and brain of SD rats. Methods: Semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) was used to detect the GPR14 mRNA. Results: In cardiovascular system, GPR14 mRNA was detected in the left ventricle, left atrium, thoratic aorta and carotid aorta. The highest level of expression was found in the left ventricle. In the brain, GPR14 mRNA was detected in cortex, hippocampus, hypothalamus and cerebellum, and higher level of expression was found in the cerebellum. Conclusion: GPR14 mRNA expression is found in the cardiovascular and neural tissues of tested rat, suggesting that urotensinⅡ may play an important role in cardiovasculature and central nervous activity.
出处 《第二军医大学学报》 CAS CSCD 北大核心 2002年第1期45-47,共3页 Academic Journal of Second Military Medical University
基金 国家"973"重点课题基金资助项目( G2 0 0 0 0 5 6 90 5 )
关键词 G蛋白偶联受体 尿紧张素类 小脑 聚合酶链反应 心血管系统 大鼠 尾加压素受体 GPR14 mRNA G-protein-coupled-receptor urotensins ventricle cerebellum polymerase chain reaction
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参考文献8

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同被引文献51

  • 1竺晓鸣,杜冠华.尾加压素Ⅱ生物学效应研究进展[J].中国药理学通报,2006,22(6):651-654. 被引量:8
  • 2钟萍,李志樑,吴宏超,唐朝枢.心力衰竭家兔尾加压素Ⅱ心肌表达的研究[J].解放军保健医学杂志,2006,8(3):144-146. 被引量:1
  • 3宋庆刚,吕建庄,杨竞霄.尾加压素Ⅱ促进乳鼠心肌成纤维细胞分泌胶原及增殖的细胞内信号转导机制[J].西安交通大学学报(医学版),2007,28(2):156-160. 被引量:3
  • 4李莉,刘亚辉,陈晓燕,郑晓敏,李瑞杰.慢性心力衰竭患者血浆尾加压素Ⅱ、脑钠肽与心功能关系的临床意义[J].临床荟萃,2007,22(11):784-785. 被引量:4
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  • 9Liu Q, Pong SS, Zeng Z, et al . Identification of urotensin Ⅱ as the endogenous ligand for the orphan G-proteincoupled receptor GPR-14[J]. Biochem Biophys Res Commun, 1999 ;266(1):174.
  • 10Chatenet D, Dubessy C, Leprince J, et al.Structure-activity relationships and structural conformation of a novel urotensin Ⅱ-related peptide[J].Peptides,2004 ;25(10): 1819.

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