To explore the hypothesis that altered vascular muscle signal transduc
tion may underlie some of the vascular changes observed in hypertensiv
e models, we measured expression of GTP-binding protein (G protein) al
pha-subunits, G(s), G(i), and G(q), in aortic muscle of reduced renal
mass and sham-operated rats and proximal and distal aortic segments fr
om rats with interrenal aortic coarctation (IR-AC). G protein expressi
on was measured by immunoblot analysis. When we probed aortic muscle m
embrane with G(i) and G(q) alpha-subunit antibodies, we identified 41-
and 42-kD immunoreactive proteins, respectively. Three immunoreactive
bands specific to G(s) alpha-subunit antibody were resolved. Immunore
active blot densities were compared. In aortic muscle membrane of redu
ced renal mass rats (blood pressure, 148+/-7 mm Hg), we found signific
antly reduced G(s) and G(i) blot densities compared with sham-operated
controls (blood pressure, 99+/-12 mm Hg). There were no differences i
n G(q) blot densities between reduced renal mass and control rats. G(s
) and G(i) blot densities were significantly lower in IR-AC proximal a
ortic segments (carotid pressure, 165+/-5 mm Hg) and distal aortic seg
ments (femoral pressure, 121+/-4 mm Hg) than in aortas of sham-operate
d controls. In contrast, G(q) expression was significantly increased i
n the high-pressure proximal aortic segments compared with low-pressur
e distal aortic segments from IR-AC rats. Thus, altered G protein expr
ession occurs in aortic muscle from nongenetic rat models of hypertens
ion. Given the differences between reduced renal mass and IR-AC models
, it is clear that pressure is not the only variable regulating G prot
ein expression and that hormonal and/or metabolic influences probably
play a larger role.