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慢性肾上腺素能受体阻断不能预防大鼠高胰岛素血症诱导的高血压。

Chronic adrenergic receptor blockade does not prevent hyperinsulinemia-induced hypertension in rats.

作者信息

Keen H L, Brands M W, Alonso-Galicia M, Hall J E

机构信息

Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson 39216-4505, USA.

出版信息

Am J Hypertens. 1996 Dec;9(12 Pt 1):1192-9. doi: 10.1016/S0895-7061(96)00254-3.

Abstract

Increased adrenergic activity has been suggested to mediate the hypertension associated with hyperinsulinemia. This study tested whether combined alpha1- and beta-adrenergic receptor blockade would prevent insulin-induced hypertension when euglycemia was maintained by continuous intravenous glucose infusion. Sprague-Dawley rats (n = 16) were instrumented with artery and vein catheters and placed in metabolic cages. Propranolol and prazosin (10 mg/kg/day each) were infused continuously intravenously in 9 rats and 7 other rats received vehicle. Mean arterial pressure (MAP) and heart rate (HR) were measured 24 h per day using computerized methods. After a control period, a 7-day intravenous infusion of insulin (1.5 microU/kg/min) was begun and glucose was coadministered intravenously at 23 mg/kg/min to prevent hypoglycemia. The MAP averaged 93 +/- 1 mm Hg in the blockade rats during the control period, which was significantly lower than the 98 +/- 1 mm Hg in the normal rats. During insulin infusion, MAP increased similarly in both groups, with a 10 +/- 2 mm Hg and 11 +/- 1 mm Hg increase in normal and blockade rats, respectively, by day 7. The HR also increased in both groups: from 417 +/- 8 beats/ min to 426 +/- 13 beats/min (P = NS) in normal rats and from 379 +/- 10 beats/min to 419 +/- 10 beats/min (P < .05) in blockade rats. Control sodium excretion averaged 2.5 +/- 0.1 mEq/day in both groups and no significant change in sodium balance was measured in either group. All variables returned toward control after stopping insulin. These results suggest that increased adrenergic activity is not required for chronic hyperinsulinemia to raise blood pressure in rats.

摘要

肾上腺素能活性增加被认为介导了与高胰岛素血症相关的高血压。本研究测试了在通过持续静脉输注葡萄糖维持血糖正常时,联合α1和β肾上腺素能受体阻断是否能预防胰岛素诱导的高血压。将16只Sprague-Dawley大鼠安装动脉和静脉导管,并置于代谢笼中。9只大鼠持续静脉输注普萘洛尔和哌唑嗪(各10mg/kg/天),另外7只大鼠接受赋形剂。每天使用计算机化方法测量平均动脉压(MAP)和心率(HR)。在对照期后,开始为期7天的胰岛素静脉输注(1.5微单位/千克/分钟),并以23毫克/千克/分钟的速度静脉联合给予葡萄糖以预防低血糖。在对照期,阻断组大鼠的MAP平均为93±1mmHg,显著低于正常大鼠的98±1mmHg。在胰岛素输注期间,两组的MAP均有相似程度的升高,到第7天,正常大鼠和阻断组大鼠的MAP分别升高了10±2mmHg和11±1mmHg。两组的HR也都增加:正常大鼠从417±8次/分钟增加到426±13次/分钟(P=无显著性差异),阻断组大鼠从379±10次/分钟增加到419±10次/分钟(P<0.05)。两组的对照期钠排泄平均为2.5±0.1mEq/天,两组的钠平衡均未测得显著变化。停止胰岛素输注后,所有变量均恢复到对照水平。这些结果表明,慢性高胰岛素血症在大鼠中升高血压并不需要肾上腺素能活性增加。

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