Experimental models of hypertension in various animals are useful in t
he research of vasoactive mechanisms. Recombinant DNA technology has p
roduced genetically engineered animals, mostly mice, useful in hyperte
nsion research. However, the development of hypertensive models in mic
e is fraught with technical difficulties. We describe here thr success
ful development in mice of two common types of experimental hypertensi
on the renovascular two-kidney, one clip and mineralocorticoid deoxyco
rticosterone-salt models. By adapting technology previously used in ra
ts, we succeeded in developing hypertension (defined as systolic press
ures higher than 140 mm Hg) in more than 50% of mice so treated. We al
so adapted the methodology for indirect tail-cuff blood pressure measu
rements as well as for direct intra-arterial monitoring of blood press
ure in conscious, freely moving mice. Application of these techniques
in transgenic or gene knockout mice with altered vasoactive hormones o
r receptors should allow elucidation of the role of the target gene pr
oducts in various types of hypertension.