Buchanan T A, Sipos G F, Madrilejo N, Liu C, Campese V M
Department of Medicine, University of Southern California Medical School, Los Angeles 90033.
Am J Physiol. 1992 Jan;262(1 Pt 1):E14-9. doi: 10.1152/ajpendo.1992.262.1.E14.
We performed euglycemic clamp studies with labeled glucose to measure insulin's effect on hepatic glucose output (HGO) and peripheral glucose clearance in eight conscious mobile spontaneously hypertensive rats (SHR) and eleven normotensive Wistar-Kyoto (WKY) rats age 9-10 wk. Systolic blood pressure was elevated in the SHR (P less than 0.001), whereas means of 12-h-fasted plasma insulin (P greater than 0.4), glucose (P greater than 0.07), HGO (P greater than 0.25), and glucose clearance (P greater than 0.2) did not differ significantly between groups. Infusions of human insulin into SHR and WKY rats (1 and 1.5 mU.min-1.kg-1, respectively) during concomitant somatostatin administration reestablished basal insulinemia in both groups. Neither HGO (P greater than 0.15) nor glucose clearance (P greater than 0.3) differed significantly between SHR and WKY rats under those conditions. Somatostatin plus higher-dose insulin infusions (4 mU.min-1.kg-1 in SHR and 3 or 6 mU.min-1.kg-1 in WKY rats) resulted in physiological hyperinsulinemia in all rats. Insulin sensitivity, calculated as the increase in glucose clearance effected by an increase in circulating insulin during higher-dose insulin infusions, did not differ significantly between SHR and WKY groups (P greater than 0.3). HGO was completely suppressed in SHR and WKY rats during the higher-dose insulin infusions. Our data indicate that hypertension is present in SHR at an age when insulin-mediated glucose disposal is not different from age-matched WKY rats. These findings do not support a role for peripheral insulin resistance in the genesis of hypertension in SHR.
我们对8只清醒、活动自如的自发性高血压大鼠(SHR)和11只9 - 10周龄的血压正常的Wistar - Kyoto(WKY)大鼠进行了用标记葡萄糖的正常血糖钳夹研究,以测量胰岛素对肝脏葡萄糖输出(HGO)和外周葡萄糖清除率的影响。SHR的收缩压升高(P < 0.001),而两组间12小时禁食血浆胰岛素(P > 0.4)、葡萄糖(P > 0.07)、HGO(P > 0.25)和葡萄糖清除率(P > 0.2)的均值无显著差异。在同时给予生长抑素的情况下,分别向SHR和WKY大鼠输注人胰岛素(分别为1和1.5 mU·min⁻¹·kg⁻¹),使两组均恢复基础胰岛素血症。在这些条件下,SHR和WKY大鼠的HGO(P > 0.15)和葡萄糖清除率(P > 0.3)均无显著差异。生长抑素加更高剂量胰岛素输注(SHR为4 mU·min⁻¹·kg⁻¹,WKY大鼠为3或6 mU·min⁻¹·kg⁻¹)使所有大鼠产生生理性高胰岛素血症。在更高剂量胰岛素输注期间,以循环胰岛素增加所引起的葡萄糖清除率增加来计算的胰岛素敏感性,SHR和WKY组之间无显著差异(P > 0.3)。在更高剂量胰岛素输注期间,SHR和WKY大鼠的HGO均被完全抑制。我们的数据表明,在SHR中出现高血压时,其胰岛素介导的葡萄糖处置与年龄匹配的WKY大鼠并无差异。这些发现不支持外周胰岛素抵抗在SHR高血压发生中起作用。