Rossetti Paolo, Porcellati Francesca, Busciantella Ricci Natalia, Candeloro Paola, Cioli Patrizia, Nair K Sreekumaran, Santeusanio Fausto, Bolli Geremia B, Fanelli Carmine G
Department of Internal Medicine, University of Perugia, Perugia, Italy.
Diabetes. 2008 Jul;57(7):1905-17. doi: 10.2337/db08-0276. Epub 2008 Apr 4.
Amino acids stimulate glucagon responses to hypoglycemia and may be utilized by the brain. The aim of this study was to assess the responses to hypoglycemia in nondiabetic and type 1 diabetic subjects after ingestion of an amino acid mixture.
Ten nondiabetic and 10 diabetic type 1 subjects were studied on three different occasions during intravenous insulin (2 mU . kg(-1) . min(-1)) plus variable glucose for 160 min. In two studies, clamped hypoglycemia (47 mg/dl plasma glucose for 40 min) was induced and either oral placebo or an amino acid mixture (42 g) was given at 30 min. In the third study, amino acids were given, but euglycemia was maintained.
Plasma glucose and insulin were no different in the hypoglycemia studies with both placebo and amino acids (P > 0.2). After the amino acid mixture, plasma amino acid concentrations increased to levels observed after a mixed meal (2.4 +/- 0.13 vs. placebo study 1.7 +/- 0.1 mmol/l, P = 0.02). During clamped euglycemia, ingestion of amino acids resulted in transient increases in glucagon concentrations, which returned to basal by the end of the study. During clamped hypoglycemia, glucagon response was sustained and increased more in amino acid studies versus placebo in nondiabetic and diabetic subjects (P < 0.05), but other counter-regulatory hormones and total symptom score were not different. Beta-OH-butyrate was less suppressed after amino acids (200 +/- 15 vs. 93 +/- 9 micromol/l, P = 0.01). Among the cognitive tests administered, the following indicated less deterioration after amino acids than placebo: Trail-Making part B, PASAT (Paced Auditory Serial Addition Test) (2 s), digit span forward, Stroop colored words, and verbal memory tests for nondiabetic subjects; and Trail-Making part B, digit span backward, and Stroop color tests for diabetic subjects.
Oral amino acids improve cognitive function in response to hypoglycemia and enhance the response of glucagon in nondiabetic and diabetic subjects.
氨基酸可刺激胰高血糖素对低血糖的反应,且可能被大脑利用。本研究旨在评估非糖尿病和1型糖尿病受试者摄入氨基酸混合物后对低血糖的反应。
10名非糖尿病受试者和10名1型糖尿病受试者在静脉输注胰岛素(2 mU·kg⁻¹·min⁻¹)加可变葡萄糖的情况下,于三个不同时段进行了160分钟的研究。在两项研究中,诱导产生钳夹性低血糖(血浆葡萄糖47 mg/dl,持续40分钟),并在30分钟时给予口服安慰剂或氨基酸混合物(42 g)。在第三项研究中,给予氨基酸,但维持血糖正常。
在低血糖研究中,给予安慰剂和氨基酸时血浆葡萄糖和胰岛素水平无差异(P>0.2)。给予氨基酸混合物后,血浆氨基酸浓度升至混合餐后观察到的水平(2.4±0.13对安慰剂研究中的1.7±0.1 mmol/l,P = 0.02)。在钳夹性血糖正常期间,摄入氨基酸导致胰高血糖素浓度短暂升高,研究结束时恢复至基础水平。在钳夹性低血糖期间,非糖尿病和糖尿病受试者中,与安慰剂相比,氨基酸研究中胰高血糖素反应持续且增加更多(P<0.05),但其他反调节激素和总症状评分无差异。氨基酸后β-羟丁酸的抑制作用较小(200±15对93±9 μmol/l,P = 0.01)。在进行的认知测试中,以下结果表明,与安慰剂相比,氨基酸后非糖尿病受试者的连线测验B部分、PASAT(听觉连续加法测验)(2秒)、顺背数字广度、斯特鲁普颜色词测验和言语记忆测试;以及糖尿病受试者的连线测验B部分、倒背数字广度和斯特鲁普颜色测验的恶化程度较小。
口服氨基酸可改善对低血糖的认知功能,并增强非糖尿病和糖尿病受试者的胰高血糖素反应。