Conrad K P, Barrera S A, Friedman P A, Schmidt V M
Department of Physiology, Dartmouth Medical School, Hanover, New Hampshire 03756.
J Clin Invest. 1991 May;87(5):1700-9. doi: 10.1172/JCI115187.
We postulated that vascular phosphoinositide metabolism is attenuated during pregnancy, and thereby could contribute to maternal vasodilation and reduced vascular reactivity. The basal rate of incorporation of [3H]myo-inositol and [3H]glycerol into phosphoinositides of aortae from pregnant rats in vitro was significantly reduced, when compared with vessels from virgin animals. After injection of [3H]myo-inositol intravenously into chronically instrumented conscious pregnant and virgin rats, the incorporation of the label by phosphatidylinositol was 66 +/- 4% less in aortae of gravid versus virgin animals (P less than 0.001), despite comparable plasma concentrations of radioactivity. Fold stimulation of total [3H]inositol phosphates by arginine vasopressin, norepinephrine, and angiotensin II over a 15-min period was not different between aortic segments from virgin and gravid rats, although both absolute basal and stimulated levels were significantly less in vessels from pregnant animals. After 45 s of incubation with 10(-7) M arginine vasopressin, however, the fold-stimulation of [3H]inositol trisplus tetrakisphosphate was reduced in aortae from gravid rats, when compared with vessels from virgin animals (P less than 0.005). By HPLC, greater than 90% of the radioactivity in the [3H]inositol trisplus tetrakisphosphate column fraction after 30 and 60 s of agonist stimulation was [3H]inositol-1,4,5-trisphosphate. We further observed that the rate of uptake of [3H]myo-inositol by aortic vasculature obtained from gravid rats was significantly (24%) less than uptake by vessels from virgin animals. Plasma myo-inositol concentrations were not significantly different, but presumably as a consequence of reduced uptake, aortic segments freshly isolated from pregnant rats contained 22 +/- 6% less myo-inositol than vessels from virgin controls as measured by gas chromatography-mass spectrometry (P less than 0.03). We conclude that myo-inositol uptake and content, phosphoinositide turnover, and inositol phosphate production are reduced in aortic vasculature of gravid rats.
我们推测,孕期血管磷酸肌醇代谢减弱,进而可能导致母体血管舒张和血管反应性降低。与未孕动物的血管相比,体外培养的孕鼠主动脉中[3H]肌醇和[3H]甘油掺入磷酸肌醇的基础速率显著降低。给长期植入仪器的清醒孕鼠和未孕鼠静脉注射[3H]肌醇后,尽管血浆放射性浓度相当,但妊娠动物主动脉中磷脂酰肌醇对标记物的掺入量比未孕动物少66±4%(P<0.001)。在15分钟内,精氨酸加压素、去甲肾上腺素和血管紧张素II对总[3H]肌醇磷酸的刺激倍数在未孕和妊娠大鼠的主动脉段之间没有差异,尽管妊娠动物血管中的绝对基础水平和刺激水平均显著较低。然而,与未孕动物的血管相比,用10(-7)M精氨酸加压素孵育45秒后,妊娠大鼠主动脉中[3H]肌醇三磷酸加四磷酸的刺激倍数降低(P<0.005)。通过高效液相色谱法,激动剂刺激30秒和60秒后,[3H]肌醇三磷酸加四磷酸柱馏分中超过90%的放射性为[3H]肌醇-1,4,5-三磷酸。我们进一步观察到,妊娠大鼠主动脉血管对[3H]肌醇的摄取速率比未孕动物的血管显著低(24%)。血浆肌醇浓度没有显著差异,但可能由于摄取减少,通过气相色谱-质谱法测定,刚从妊娠大鼠分离的主动脉段所含肌醇比未孕对照血管少22±6%(P<0.03)。我们得出结论,妊娠大鼠主动脉血管中肌醇摄取和含量、磷酸肌醇周转以及肌醇磷酸生成均减少。