Chao J, Jin L, Lin K F, Chao L
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston 29425, USA.
Hypertens Res. 1997 Dec;20(4):269-77. doi: 10.1291/hypres.20.269.
Adrenomedullin (ADM) is a potent vasoactive peptide. In this study, we explored the effects of a continuous supply of ADM by somatic gene delivery on spontaneously hypertensive rats (SHR). DNA constructs containing the human ADM cDNA fused to either the cytomegalovirus promoter (CMV-cADM) or Rous Sarcoma virus 3'-long terminal repeat (RSV-cADM) were intravenously injected into SHR through the tail vein. Expression of human ADM in SHR was identified in the kidney, adrenal gland, heart, and lung by radioimmunoassay and reverse transcription-polymerase chain reaction followed by Southern blot analysis. A single injection of ADM plasmid DNA in young adult SHR (7 wk old) caused a significant reduction in systolic blood pressure for up to 5 wk (p < 0.05). A second injection of CMV-cADM 5 wk after the first delivery resulted in a further reduction in blood pressure for another 3 wk (p < 0.001). A maximal blood pressure reduction of 22 mmHg in SHR was observed 7 wk after injection of CMV-cADM plasmid DNA (185 +/- 1.7 mmHg, n = 6, p < 0.001), and a reduction of 15 mmHg was observed after injection of RSV-cADM (192 +/- 2.7 mmHg, n = 6, p < 0.001), as compared with control rats given vector DNA (207 +/- 2.4 mmHg, n = 6). Similarly, injection of CMV-cADM plasmid DNA in adult SHR (10 wk old) resulted in a significant reduction in blood pressure for up to 6 wk. Antibodies to either human ADM or its plasmid DNA were not detected in rat sera after the second injection. These studies indicate that intravenous injection of the human ADM gene in hypertensive rats results in expression of the foreign gene and induces a long-lasting reduction in blood pressure.
肾上腺髓质素(ADM)是一种强效血管活性肽。在本研究中,我们探讨了通过体细胞基因递送持续供应ADM对自发性高血压大鼠(SHR)的影响。将含有与人巨细胞病毒启动子(CMV-cADM)或劳斯肉瘤病毒3'-长末端重复序列(RSV-cADM)融合的人ADM cDNA的DNA构建体通过尾静脉静脉注射到SHR中。通过放射免疫分析、逆转录-聚合酶链反应以及随后的Southern印迹分析,在SHR的肾脏、肾上腺、心脏和肺中鉴定出人ADM的表达。在年轻成年SHR(7周龄)中单次注射ADM质粒DNA可使收缩压显著降低长达5周(p<0.05)。首次给药5周后第二次注射CMV-cADM可使血压在另外3周内进一步降低(p<0.001)。注射CMV-cADM质粒DNA 7周后,SHR的最大血压降低了22 mmHg(185±1.7 mmHg,n = 6,p<0.001),注射RSV-cADM后降低了15 mmHg(192±2.7 mmHg,n = 6,p<0.001),而给予载体DNA的对照大鼠血压为207±2.4 mmHg(n = 6)。同样,在成年SHR(10周龄)中注射CMV-cADM质粒DNA可使血压显著降低长达6周。第二次注射后在大鼠血清中未检测到针对人ADM或其质粒DNA的抗体。这些研究表明,在高血压大鼠中静脉注射人ADM基因可导致外源基因表达并诱导血压长期降低。