Carpentier A, Giacca A, Lewis G F
Department of Medicine, Division of Endocrinology, University of Toronto, Toronto General Hospital, Toronto, Ontario, Canada.
Diabetologia. 2001 Nov;44(11):1989-97. doi: 10.1007/s001250100002.
AIMS/HYPOTHESIS: We have shown previously that the increase of plasma non-esterified fatty acids for 48 h results in decreased glucose-stimulated insulin secretion in lean and non-diabetic obese subjects. It is currently not known if a prolonged increase in non-esterified fatty acids also impairs the insulin secretory response to non-glucose secretagogues.
Heparin and intralipid (to increase plasma non-esterified fatty acid concentrations by about two- to fourfold) or normal saline was infused intravenously for 48 h in 14 non-diabetic obese subjects. On the third day in both studies, insulin, C-peptide, proinsulin, and insulin secretion rate were assessed in response to an intravenous arginine infusion at fasting glucose concentration and a second arginine infusion after a 60-min 11 mmol/l hyperglycaemic clamp.
There were no significant differences detected in acute (5 min) or total (90 min) arginine-stimulated C-peptide or insulin secretion response in the heparin-intralipid study compared with the control group at fasting glucose or during hyperglycaemia.
CONCLUSION/INTERPRETATION: We have shown that a prolonged increase in plasma NEFA does not blunt arginine-stimulated insulin secretion or plasma insulin concentrations in non-diabetic obese subjects. These findings suggest that the previously demonstrated NEFA-induced impairment in insulin secretory response to glucose cannot be generalized for non-glucose secretagogues.
目的/假设:我们之前已经表明,在瘦型和非糖尿病肥胖受试者中,血浆非酯化脂肪酸水平升高48小时会导致葡萄糖刺激的胰岛素分泌减少。目前尚不清楚非酯化脂肪酸的长期升高是否也会损害对非葡萄糖促分泌剂的胰岛素分泌反应。
对14名非糖尿病肥胖受试者静脉输注肝素和脂乳剂(使血浆非酯化脂肪酸浓度增加约2至4倍)或生理盐水,持续48小时。在两项研究的第三天,在空腹血糖浓度下静脉输注精氨酸以及在60分钟11 mmol/l高血糖钳夹后再次输注精氨酸后,评估胰岛素、C肽、胰岛素原和胰岛素分泌率。
与对照组相比,在空腹血糖或高血糖期间,肝素-脂乳剂研究中急性(5分钟)或总(90分钟)精氨酸刺激的C肽或胰岛素分泌反应没有显著差异。
结论/解读:我们已经表明,血浆非酯化脂肪酸的长期升高不会减弱非糖尿病肥胖受试者中精氨酸刺激的胰岛素分泌或血浆胰岛素浓度。这些发现表明,先前证明的非酯化脂肪酸诱导的对葡萄糖的胰岛素分泌反应受损不能推广到非葡萄糖促分泌剂。