Weiner C P, Lizasoain I, Baylis S A, Knowles R G, Charles I G, Moncada S
Wellcome Research Laboratories, Beckenham Kent, United Kingdom.
Proc Natl Acad Sci U S A. 1994 May 24;91(11):5212-6. doi: 10.1073/pnas.91.11.5212.
We have examined the effects of pregnancy and sex hormones on calcium-dependent and calcium-independent nitric oxide synthases (NOSs) in the guinea pig. Pregnancy (near term) caused a > 4-fold increase in the activity of calcium-dependent NOS in the uterine artery and at least a doubling in the heart, kidney, skeletal muscle, esophagus, and cerebellum. The increase in NOS activity in the cerebellum during pregnancy was inhibited by the estrogen-receptor antagonist tamoxifen. Treatment with estradiol (but not progesterone) also increased calcium-dependent NOS activity in the tissues examined from both females and males. Testosterone increased calcium-dependent NOS only in the cerebellum. No significant change in calcium-independent NOS activity was observed either during pregnancy or after the administration of any sex hormone. Both pregnancy and estradiol treatment increased the amount of mRNAs for NOS isozymes eNOS and nNOS in skeletal muscle, suggesting that the increases in NOS activity result from enzyme induction. Thus both eNOS and nNOS are subject to regulation by estrogen, an action that could explain some of the changes that occur during pregnancy and some gender differences in physiology and pathophysiology.
我们研究了妊娠和性激素对豚鼠钙依赖性和非钙依赖性一氧化氮合酶(NOSs)的影响。妊娠(接近足月)导致子宫动脉中钙依赖性NOS的活性增加超过4倍,心脏、肾脏、骨骼肌、食管和小脑中至少增加一倍。妊娠期间小脑NOS活性的增加被雌激素受体拮抗剂他莫昔芬抑制。雌二醇(而非孕酮)处理也增加了来自雌性和雄性的所检测组织中钙依赖性NOS的活性。睾酮仅增加小脑中钙依赖性NOS的活性。在妊娠期间或给予任何性激素后,未观察到非钙依赖性NOS活性有显著变化。妊娠和雌二醇处理均增加了骨骼肌中NOS同工酶eNOS和nNOS的mRNA量,提示NOS活性的增加是由酶诱导所致。因此,eNOS和nNOS均受雌激素调节,这一作用可以解释妊娠期间发生的一些变化以及生理和病理生理学中的一些性别差异。