Bunnag P, Hori M T, Ormsby B, Berger M E, Golub M S, Tuck M L
Division of Endocrinology, Department of Veterans Affairs Medical Center, Sepulveda, CA 91343, USA.
Hypertens Res. 1997 Mar;20(1):17-21. doi: 10.1291/hypres.20.17.
This study was conducted to investigate whether altered vascular responsiveness to vasoactive compounds contributes to the development of hypertension in diet-induced hyperinsulinemic rats. Male Sprague-Dawley rats were randomly assigned to receive high fructose, high sucrose, or standard rat chow for 13-18 wk. Blood pressure was monitored by indirect (tail-cuff) measurements at regular intervals during the diet treatment. Vascular responses to various vasoactive agents were studied both in vivo and in vitro. Blood pressure response, as assessed by direct (intra-arterial) measurement, to graded dose infusions of norepinephrine or angiotensin II or bolus infusion of acetylcholine were determined. In vitro vascular responses of the tail arteries to exogenous norepinephrine were also studied. The fructose- and the sucrose-fed rats had significantly higher blood pressure than controls. Serum insulin levels were also significantly higher in fructose- and sucrose-fed rats than in controls. The blood pressure responses to graded infusions of norepinephrine were significantly less in the fructose-fed rats than in controls. The blood pressure responses to angiotensin II and acetylcholine infusion were not significantly different among the three groups of rats. In vitro studies of vascular reactivity in the tail arteries revealed than the concentration of norepinephrine that produced half-maximal contraction (NE EC50) was significantly higher in the fructose group than control. Thus, impaired vascular responses to exogenous norepinephrine were observed in fructose-fed rats both in vivo and in vitro. This may be due to an adaptation to increased sympathetic nervous activity, or may be a compensatory response to other structural or functional changes that produce hypertension in this model.
本研究旨在探讨血管对血管活性化合物反应性的改变是否会导致饮食诱导的高胰岛素血症大鼠发生高血压。将雄性Sprague-Dawley大鼠随机分为三组,分别给予高果糖、高蔗糖或标准大鼠饲料,持续13 - 18周。在饮食治疗期间,定期通过间接(尾套法)测量监测血压。对各种血管活性药物的血管反应在体内和体外进行了研究。通过直接(动脉内)测量评估血压对去甲肾上腺素或血管紧张素II分级剂量输注或乙酰胆碱推注的反应。还研究了尾动脉对体外给予去甲肾上腺素的血管反应。喂食果糖和蔗糖的大鼠血压显著高于对照组。喂食果糖和蔗糖的大鼠血清胰岛素水平也显著高于对照组。喂食果糖的大鼠对去甲肾上腺素分级输注的血压反应明显低于对照组。三组大鼠对血管紧张素II和乙酰胆碱输注的血压反应无显著差异。尾动脉血管反应性的体外研究显示,果糖组产生半数最大收缩的去甲肾上腺素浓度(NE EC50)显著高于对照组。因此,在喂食果糖的大鼠体内和体外均观察到对外源性去甲肾上腺素的血管反应受损。这可能是由于对交感神经活动增加的适应,也可能是对该模型中导致高血压的其他结构或功能变化的代偿反应。