17β-Estradiol Alters Isoproterenol-Induced Relaxation in Rat Aortic Rings

[摘要] References(15)Cited-By(6)Female Wistar rats were treated with 17β-estradiol (E2) (10 μg, s.c.) or with sesame oil for 3 days. The relaxation induced by isoproterenol (10-9-3×10-6 M) in aortae precontracted with norepinephrine was significantly suppressed in aortae from E2-treated rats compared with the relaxation in those from control rats. NG-Nitro-L-arginine, a nitric oxide synthase inhibitor, inhibited isoproterenol-induced relaxation in aortae from both E2-treated and control rats. Metyrapone, a cytochrome P-450 monooxygenase inhibitor, inhibited it in aortae from control rats, but metyrapone enhanced the maximum relaxation in aortae from E2-treated rats. These results suggest that E2 modulates isoproterenol-induced vasodilation through nitric oxide and cytochrome P-450-dependent metabolites.

[学科分类] 药理学

[关键词] Cytochrome P-450;Isoproterenol;17β-Estradiol