Estrogen Ameliorates N(superscript ω)-nitro-L-arginine Methy1 Ester-induced Blood Pressure Increment in Male Spontaneously Hypertensive Rats: The Role of cGMP

Chia-Hung Yen；Yu-Ren Wang；Chiu-Feng Huang；Ying-Tung Lau

blood pressure ； estradiol ； nitric oxide ； cyclic guanosine monophosphate ； spontaneously hypertensive rats

The Chinese Journal of Physiology

47卷4期（2004 / 12 / 31）

183 - 187

英文

Estrogen (17beta-estradiol, or E2) reduces systolic blood pressure (SBP) increment and increases aortic cyclic guanosine monophosphate (cGMP) in male spontaneously hypertensive rats (SHRs). It is unknown, however, whether the E2-enhanced aortic cGMP is essential for the BP-lowering effect or not. N(superscript ω)-nitro-L-arginine-methy1 ester (L-NAME), an L-arginine analogue and nitric oxide (NO) synthase inhibitor, significantly increases SBP and decreases aortic cGMP in male SHRs. We thus treated male SHRs with vehicle (corn oil) or E2 (s.c, 2 mg/kg/week) with or without L-NAME (20 mg/dl in the drinking water). SBP was measured weekly. Plasma nitrate/Nitrite (NOx) concentrations and aortic cGMP levels were all measured at the end of the study. We found that SBP increment was significantly higher in L-NAME group, compared with the controls, and that E2 treatment reduced this L-NAME effect. Plasma NOx concentrations were not significantly different among different groups. Basal and acetylcholine induced aortic cGMP, but not sodium nitroprusside-induced cGMP, were significantly lower in L-NAME group, compared with the controls. E2 co-administration did not modify L-NAME-induced aortic cGMP decrease. These data indicate that E2-induced BP-lowering effect in L-NAME treated male SHRs is not closely associated with the enhancement of vascular cGMP.