Xiao C, Giacca A, Carpentier A, Lewis G F
Department of Medicine and Physiology, University of Toronto, Toronto, ON, Canada.
Diabetologia. 2006 Jun;49(6):1371-9. doi: 10.1007/s00125-006-0211-x. Epub 2006 Apr 5.
AIMS/HYPOTHESIS: Prolonged elevation of plasma specific fatty acids may exert differential effects on glucose-stimulated insulin secretion (GSIS), insulin sensitivity and clearance.
We examined the effect of oral ingestion, at regular intervals for 24 h, of an emulsion containing either predominantly monounsaturated (MUFA), polyunsaturated (PUFA) or saturated (SFA) fat or water (control) on GSIS, insulin sensitivity and insulin clearance in seven overweight or obese, non-diabetic humans. Four studies were conducted in each individual in random order, 4-6 weeks apart. Twenty-four hours after initiation of oral ingestion, subjects underwent a 2 h, 20 mmol/l hyperglycaemic clamp to assess GSIS, insulin sensitivity and insulin clearance.
Following oral ingestion of any of the three fat emulsions over 24 h, plasma NEFAs were elevated by approximately 1.5- to 2-fold over the basal level. Ingestion of any of the three fat emulsions resulted in reduction in insulin clearance, and SFA ingestion reduced insulin sensitivity. PUFA ingestion was associated with an absolute reduction in GSIS, whereas insulin secretion failed to compensate for insulin resistance in subjects who ingested SFA.
CONCLUSIONS/INTERPRETATION: Oral ingestion of fats with differing degrees of saturation resulted in different effects on insulin secretion and action. PUFA ingestion resulted in an absolute reduction in insulin secretion and SFA ingestion induced insulin resistance. Failure of insulin secretion to compensate for insulin resistance implies impaired beta cell function in the SFA study.
目的/假设:血浆特定脂肪酸的长期升高可能对葡萄糖刺激的胰岛素分泌(GSIS)、胰岛素敏感性和清除率产生不同影响。
我们研究了7名超重或肥胖的非糖尿病患者每隔24小时定时口服包含主要为单不饱和脂肪酸(MUFA)、多不饱和脂肪酸(PUFA)或饱和脂肪酸(SFA)的脂肪乳剂或水(对照)对GSIS、胰岛素敏感性和胰岛素清除率的影响。每位受试者按随机顺序进行4项研究,每项研究间隔4 - 6周。在开始口服24小时后,受试者接受2小时、20 mmol/l的高血糖钳夹试验以评估GSIS、胰岛素敏感性和胰岛素清除率。
在24小时内口服三种脂肪乳剂中的任何一种后,血浆非酯化脂肪酸(NEFAs)比基础水平升高了约1.5至2倍。摄入三种脂肪乳剂中的任何一种都会导致胰岛素清除率降低,摄入SFA会降低胰岛素敏感性。摄入PUFA与GSIS的绝对降低有关,而在摄入SFA的受试者中胰岛素分泌未能补偿胰岛素抵抗。
结论/解读:口服不同饱和度的脂肪对胰岛素分泌和作用产生不同影响。摄入PUFA导致胰岛素分泌绝对减少,摄入SFA诱导胰岛素抵抗。在SFA研究中胰岛素分泌未能补偿胰岛素抵抗意味着β细胞功能受损。