Chao J, Chao L
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston 29425-2211, USA.
Pharmacol Res. 1997 Jun;35(6):517-22. doi: 10.1006/phrs.1997.0179.
Hypertension is a multi-gene and multi-factorial disorder affecting about 25% of the population. Hypertensive subjects are more likely to develop other cardiovascular diseases such as peripheral vascular disease, coronary heart disease, congestive heart failure and cerebrovascular disease. To demonstrate potential therapeutic effects of somatic gene delivery in treating hypertension, we delivered human tissue kallikrein in the form of naked DNA or in an adenovirus vector into hypertensive rats. Naked DNA constructs were delivered into spontaneously hypertensive rats via intramuscular, intravenous, intraportal vein and intraperitoneal routes. A single injection of human kallikrein DNA construct caused a sustained reduction of blood pressure which began 1 week post-injection and continued for more than 6 weeks. The hypotensive effect caused by somatic gene delivery of human tissue kallikrein in hypertensive rats is reversed by aprotinin, a potent tissue kallikrein inhibitor. Both systemic and local delivery of the human tissue kallikrein gene in an adenovirus vector were found to be highly effective in producing a rapid and sustained reduction of blood pressure in hypertensive rat models such as spontaneously hypertensive rats; two kidney, one clip Goldblatt hypertensive rats; and Dahl salt-sensitive rats. The expression of human tissue kallikrein in rats was identified in the heart, kidney, aorta, lung and liver by reverse transcription-polymerase chain reaction followed by Southern blot analysis and by ELISA. Adenovirus-mediated kallikrein gene delivery also resulted in the attenuation of glomerular and tubular damage and reduction of the left ventricular mass and cardiomyocyte size in Dahl salt-sensitive rats fed a high salt diet. The ability of kallikrein gene delivery to produce a wide spectrum of beneficial effects makes it an excellent candidate in treating salt-related hypertension as well as cardiovascular and renal diseases. These results suggest the feasibility of applying somatic gene therapy for treating hypertension and salt-related cardiovascular and renal disorders.
高血压是一种多基因、多因素疾病,影响着约25%的人口。高血压患者更易患其他心血管疾病,如外周血管疾病、冠心病、充血性心力衰竭和脑血管疾病。为了证明体细胞基因传递在治疗高血压方面的潜在治疗效果,我们将人组织激肽释放酶以裸DNA或腺病毒载体的形式导入高血压大鼠体内。裸DNA构建体通过肌肉内、静脉内、门静脉内和腹膜内途径导入自发性高血压大鼠体内。单次注射人激肽释放酶DNA构建体可使血压持续降低,注射后1周开始,持续超过6周。在高血压大鼠中,通过体细胞基因传递人组织激肽释放酶所产生的降压作用可被抑肽酶(一种有效的组织激肽释放酶抑制剂)逆转。发现在腺病毒载体中全身和局部递送人组织激肽释放酶基因在诸如自发性高血压大鼠、二肾一夹型Goldblatt高血压大鼠和Dahl盐敏感大鼠等高血压大鼠模型中能非常有效地使血压快速且持续降低。通过逆转录 - 聚合酶链反应,随后进行Southern印迹分析和ELISA,在大鼠的心脏、肾脏、主动脉、肺和肝脏中鉴定出人组织激肽释放酶的表达。在高盐饮食喂养的Dahl盐敏感大鼠中,腺病毒介导的激肽释放酶基因传递还导致肾小球和肾小管损伤减轻,左心室质量和心肌细胞大小减小。激肽释放酶基因传递产生广泛有益作用的能力使其成为治疗盐相关性高血压以及心血管和肾脏疾病的极佳候选者。这些结果表明应用体细胞基因疗法治疗高血压以及盐相关性心血管和肾脏疾病的可行性。