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(Hypertension. 2001;38:543.)
© 2001 American Heart Association, Inc.

Genetics and Gene Therapy

Gene Therapy for Hypertension

The Preclinical Data

M. Ian Phillips

Department of Physiology, College of Medicine, University of Florida, Gainesville.

M. Ian Phillips, PhD, DSc, Department of Physiology, College of Medicine, Box 100274, University of Florida, Gainesville, FL 32610-0274. E-Mail MIP{at}phys.med.ufl.edu

Abstract

Abstract—— Despite several drugs for the treatment of hypertension, there are many patients with poorly controlled high blood pressure. This is partly because all of the available drugs are short-lasting (24 hours), have side effects, and are not highly specific. Gene therapy offers a possibility of producing longer-lasting effects with precise specificity based on the genetic design. Preclinical studies on gene therapy for hypertension have taken 2 approaches. Chao et al have performed extensive studies on gene transfer to increase vasodilator proteins. They have transferred kallikrein, atrial natriuretic peptide, adrenomedullin, and endothelin NO synthase into different rat models. Their results show that blood pressure can be lowered for 3 to 12 weeks with the expression of these genes. The antisense approach, which we began by targeting angiotensinogen and the angiotensin type 1 (AT₁) receptor, has now been tested independently by several different groups in multiple models of hypertension. Other genes targeted include the ß₁-adrenoceptor, thyrotropin-releasing hormone, angiotensin gene-activating elements, carboxypeptidase Y, c-fos, and CYP4A1. There have been 2 methods of delivering antisense: one is by oligodeoxynucleotides, and the other is with full-length DNA in viral vectors. All the studies show a decrease in blood pressure lasting several days to weeks or months. Oligos are safe and nontoxic and could be delivered orally or eventually by skin patches. Systemic delivery of recombinant adeno-associated virus with DNA antisense to AT₁ receptors in adult rodents decreases hypertension for up to 6 months. We conclude that there is sufficient preclinical data to give serious consideration to phase I trials for testing some of the antisense oligodeoxynucleotides, although testing the viral vectors needs much more work.

Key Words: genes • drug therapy • kallkirein • renin angiotensin system • adrenergic receptor blockers • oligonucleotides • antisense • adeno-associated virus

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