Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
Diabetes. 2010 Apr;59(4):1074-81. doi: 10.2337/db09-1520. Epub 2010 Jan 19.
To date, there are no data investigating the effects of GABA(A) activation on counterregulatory responses during repeated hypoglycemia in humans. The aim of this study was to determine the effects of prior GABA(A) activation using the benzodiazepine alprazolam on the neuroendocrine and autonomic nervous system (ANS) and metabolic counterregulatory responses during next-day hypoglycemia in healthy humans.
Twenty-eight healthy individuals (14 male and 14 female, age 27 +/- 6 years, BMI 24 +/- 3 kg/m(2), and A1C 5.2 +/- 0.1%) participated in four randomized, double-blind, 2-day studies. Day 1 consisted of either morning and afternoon 2-h hyperinsulinemic euglycemia or 2-h hyperinsulinemic hypoglycemia (2.9 mmol/l) with either 1 mg alprazolam or placebo administered 30 min before the start of each clamp. Day 2 consisted of a single-step hyperinsulinemic-hypoglycemic clamp of 2.9 mmol/l.
Despite similar hypoglycemia (2.9 +/- 1 mmol/l) and insulinemia (672 +/- 108 pmol/l) during day 2 studies, GABA(A) activation with alprazolam during day 1 euglycemia resulted in significant blunting (P < 0.05) of ANS (epinephrine, norepinephrine, muscle sympathetic nerve activity, and pancreatic polypeptide), neuroendocrine (glucagon and growth hormone), and metabolic (glucose kinetics, lipolysis, and glycogenolysis) counterregulatory responses. GABA(A) activation with alprazolam during prior hypoglycemia caused further significant (P < 0.05) decrements in subsequent glucagon, growth hormone, pancreatic polypeptide, and muscle sympathetic nerve activity counterregulatory responses.
Alprazolam activation of GABA(A) pathways during day 1 hypoglycemia can play an important role in regulating a spectrum of key physiologic responses during subsequent (day 2) hypoglycemia in healthy man.
迄今为止,尚无研究探讨在人类反复低血糖期间,GABA(A) 激活对代偿性反应的影响。本研究旨在确定苯二氮䓬类药物阿普唑仑预先激活 GABA(A) 对健康人体次日低血糖期间神经内分泌和自主神经系统 (ANS) 及代谢代偿反应的影响。
28 名健康个体(14 名男性和 14 名女性,年龄 27 +/- 6 岁,BMI 24 +/- 3 kg/m(2),A1C 5.2 +/- 0.1%)参加了四项随机、双盲、2 天的研究。第 1 天包括上午和下午 2 小时高胰岛素正常血糖或 2 小时高胰岛素低血糖(2.9 mmol/l),在开始每个钳夹前 30 分钟给予 1 毫克阿普唑仑或安慰剂。第 2 天进行单次高胰岛素-低血糖钳夹,血糖为 2.9 mmol/l。
尽管第 2 天研究期间的低血糖(2.9 +/- 1 mmol/l)和胰岛素血症(672 +/- 108 pmol/l)相似,但第 1 天正常血糖期间阿普唑仑激活 GABA(A)导致 ANS(肾上腺素、去甲肾上腺素、肌肉交感神经活动和胰多肽)、神经内分泌(胰高血糖素和生长激素)和代谢(葡萄糖动力学、脂肪分解和糖原分解)代偿性反应明显减弱(P < 0.05)。第 1 天低血糖期间阿普唑仑激活 GABA(A)导致随后的胰高血糖素、生长激素、胰多肽和肌肉交感神经活动代偿性反应进一步显著降低(P < 0.05)。
第 1 天低血糖期间阿普唑仑激活 GABA(A)途径可能在调节健康男性随后(第 2 天)低血糖期间一系列关键生理反应中发挥重要作用。