Hulman S, Brodsky N, Miller J, Donnelly C, Helms J, Falkner B
Department of Pediatrics, Albert Einstein Medical Center, Philadelphia, PA 19141-3098, USA.
Am J Hypertens. 1996 Dec;9(12 Pt 1):1200-5. doi: 10.1016/S0895-7061(96)00304-4.
We have previously shown that juvenile Sprague-Dawley rats, fed a diet in which complex carbohydrates are replaced by sucrose, develop insulin resistance and hypertension. These conditions develop despite the absence of genetic predisposition to either. When studied with the euglycemic hyperinsulinemic clamp technique, these rats have reduced insulin-stimulated glucose utilization, but normal suppression of hepatic glucose output. In the young sucrose-fed rats, it was noted that the degree of blood pressure elevation was greater in males than in females. The purpose of this study was to test the hypothesis that estrogen withdrawal increases insulin resistance and hypertension. Female rats were randomized at weaning (3 weeks of life) to receive control diet or sucrose diet. Animals were assessed with weekly weight and indirect tail-cuff blood pressure. At 8 weeks of life, the sucrose-fed rats were randomized to receive bilateral oophorectomy or sham surgery (anesthesia and uterine horn exposure without removal of the ovaries). At 13 to 14 weeks of life, all animals were fasted overnight, and had an oral glucose tolerance test while conscious. Weight and weight gain were not different among the groups over the 11 week study period. Animals fed the sucrose diet developed significantly higher blood pressure than animals fed the control diet; oophorectomized animals had higher blood pressure than sham-operated animals (P <.0001). Sucrose-fed oophorectomized animals developed fasting and glucose-stimulated hyperinsulinemia. Estrogen withdrawal augments blood pressure in juvenile rats made insulin resistant and hypertensive with a sucrose diet. Estrogen withdrawal in these animals also induces fasting and glucose-stimulated hyperinsulinemia, which are signs of worsening insulin resistance. Androgen:estrogen imbalance increases metabolic dysfunction and worsens hypertension in this animal model.
我们之前已经表明,幼年斯普拉格-道利大鼠食用一种用蔗糖替代复合碳水化合物的饮食后,会出现胰岛素抵抗和高血压。尽管没有这两种疾病的遗传易感性,但这些情况还是出现了。当用正常血糖高胰岛素钳夹技术进行研究时,这些大鼠胰岛素刺激的葡萄糖利用率降低,但肝脏葡萄糖输出的正常抑制功能存在。在幼年食用蔗糖的大鼠中,注意到雄性大鼠的血压升高程度大于雌性大鼠。本研究的目的是检验雌激素撤退会增加胰岛素抵抗和高血压这一假设。雌性大鼠在断奶时(3周龄)被随机分为接受对照饮食或蔗糖饮食。每周对动物的体重和间接尾袖血压进行评估。在8周龄时,食用蔗糖的大鼠被随机分为接受双侧卵巢切除术或假手术(麻醉并暴露子宫角但不切除卵巢)。在13至14周龄时,所有动物过夜禁食,并在清醒状态下进行口服葡萄糖耐量试验。在11周的研究期间,各组之间的体重和体重增加没有差异。食用蔗糖饮食的动物血压明显高于食用对照饮食的动物;卵巢切除的动物血压高于假手术动物(P<.0001)。食用蔗糖且卵巢切除动物出现空腹和葡萄糖刺激的高胰岛素血症。雌激素撤退会使食用蔗糖饮食而产生胰岛素抵抗和高血压的幼年大鼠血压升高。这些动物的雌激素撤退还会诱发空腹和葡萄糖刺激的高胰岛素血症,这是胰岛素抵抗恶化的迹象。在这个动物模型中,雄激素与雌激素失衡会增加代谢功能障碍并使高血压恶化。