Adler G K, Majzoub J A
J Clin Endocrinol Metab. 1987 Jul;65(1):116-21. doi: 10.1210/jcem-65-1-116.
We studied the influence of a hypertonic saline infusion on the counterregulatory response to insulin-induced hypoglycemia in nine normal men. When given hypertonic saline, the men had less hypoglycemia in response to insulin, both acutely and in the recovery phase (P less than 0.01), and released 34% more glucagon (P less than 0.05) than when they were water loaded. The total integrated ACTH, cortisol, epinephrine, norepinephrine, and GH responses to hypoglycemia were similar after saline and water loading. After the saline load, the mean plasma vasopressin level rose from 11.0 +/- 2.2 (+/- SEM) to 20.9 +/- 2.9 pg/mL in response to insulin-induced hypoglycemia. In contrast, after the water load, vasopressin levels were undetectable (less than 2 pg/mL) and they increased only to 2.6 +/- 0.4 pg/mL with hypoglycemia. There was a significant positive correlation between basal plasma vasopressin and nadir glucose concentrations and a significant negative correlation between basal plasma vasopressin and the integrated fall in glucose after insulin administration (P less than 0.01 and P less than 0.025, respectively). The difference in the glycemic response to insulin may be related to the high vasopressin levels after saline loading, which could, either directly and/or through enhanced glucagon release, increase hepatic glucose production and thus limit the hypoglycemic response to insulin.
我们研究了高渗盐水输注对9名正常男性胰岛素诱导低血糖反调节反应的影响。给予高渗盐水时,男性对胰岛素的急性和恢复阶段低血糖反应均减轻(P<0.01),且与给予水负荷时相比,胰高血糖素释放增加34%(P<0.05)。盐水负荷和水负荷后,对低血糖的促肾上腺皮质激素、皮质醇、肾上腺素、去甲肾上腺素和生长激素的总综合反应相似。盐水负荷后,胰岛素诱导低血糖时,平均血浆血管加压素水平从11.0±2.2(±SEM)pg/mL升至20.9±2.9 pg/mL。相比之下,水负荷后,血管加压素水平检测不到(<2 pg/mL),低血糖时仅升至2.6±0.4 pg/mL。基础血浆血管加压素与最低血糖浓度之间存在显著正相关,基础血浆血管加压素与胰岛素给药后血糖的综合下降之间存在显著负相关(分别为P<0.01和P<0.025)。对胰岛素的血糖反应差异可能与盐水负荷后较高的血管加压素水平有关,其可直接和/或通过增强胰高血糖素释放增加肝葡萄糖生成,从而限制对胰岛素的低血糖反应。