Does sex influence circulating and renal RAAS components and blood pressure in hypertensive mRen(2).Lewis and normotensive Lewis rats?
Sex differences in circulating and renal RAAS components are primarily evident in hypertensive mRen(2).Lewis rats, with males showing enhanced RAAS activity that may contribute to higher blood pressure.
Sex differences in blood pressure are evident in experimental models and human subjects, yet the mechanisms underlying this disparity remain equivocal. The current study sought to define the extent of male-female differences in the circulating and tissue renin-angiotensin aldosterone systems (RAASs) of congenic mRen(2). Lewis and control Lewis rats. Male congenics exhibited higher systolic blood pressure than females 200 +/- 4 vs. 146 +/- 7 mmHg, P 0.05. Plasma ANG II levels were twofold higher in male congenics 47 +/- 3 vs. 19 +/- 3 pM, P < 0.01 and fivefold higher than in male or female Lewis rats 6 +/- 1 vs. 6 +/- 1 pM. ANG I levels were also highest in the males; however, plasma ANG-(1-7) was higher in female congenics. Male congenics exhibited greater circulating renin and angiotensin-converting enzyme (ACE) activities, as well as angiotensinogen, than female littermates. Renal cortical and medullary ANG II levels were also higher in the male congenics versus all the other groups; ANG I was lower in the males. Cortical ACE2 activity was higher in male congenics, yet neprilysin activity and protein were greater in the females, which may contribute to reduced renal levels of ANG II. These data reveal that sex differences in both the circulating and renal RAAS are apparent primarily in the hypertensive group. The enhanced activity of the RAAS in male congenics may contribute to the higher pressure and tissue injury evident in the strain.
Pendergrass et al. (Sun,) studied this question.