Endocrine Research Unit, Mayo Clinic, 200 1st Street SW, Rochester, Minnesota 55905, USA.
J Clin Endocrinol Metab. 2012 Mar;97(3):819-27. doi: 10.1210/jc.2011-2486. Epub 2011 Dec 14.
Endocannabinoid receptor 1 blockade is proposed to improve metabolic complications of obesity via central and peripheral effects.
Our objective was to test whether rimonabant improves insulin regulation of free fatty acid and glucose metabolism after controlling for fat loss.
This was a double-blind, placebo-controlled substudy of the visceral fat reduction assessed by computed tomography scan on rimonabant (VICTORIA) trial.
Sixty-seven abdominally obese, metabolic syndrome volunteers age 35-70 yr participated at academic medical center general clinical research centers.
Intervention included a 12-month lifestyle weight management program plus rimonabant 20 mg/d or placebo.
Body composition and two-step euglycemic, hyperinsulinemic clamp before and after intervention were performed. Insulin sensitivity was assessed as insulin concentration needed to suppress by 50% palmitate concentration [IC50(palmitate)], flux [IC50(palmitate)f], and hepatic glucose output [IC50(HGO)] and as insulin-stimulated glucose disposal (Δ glucose disappearance per Δ insulin concentration--glucose slope).
Body fat decreased by 4.5±2.9% (SD) in the rimonabant and 1.9±4.5% in the placebo group (P<0.005). The primary [improvement in IC50(palmitate) and IC50(palmitate)f] and secondary [improvement in IC50(HGO) and glucose slope] outcomes were not significantly different between the rimonabant and placebo groups. Post hoc analyses revealed that 1) changes in body mass index (BMI) and IC50(palmitate) were correlated (P=0.005) in the rimonabant group; this relationship was not significantly different from placebo when controlling for greater BMI loss (P=0.5); 2) insulin-regulated glucose disposal improved in both groups (P=0.002) and correlated with changes in BMI.
Improvements observed in insulin regulation of free fatty acid and glucose metabolism with rimonabant treatment in humans was not greater than that predicted by weight loss alone.
内源性大麻素受体 1 阻断被认为通过中枢和外周作用改善肥胖的代谢并发症。
我们的目的是在控制脂肪损失的情况下,测试是否利莫那班改善胰岛素对游离脂肪酸和葡萄糖代谢的调节作用。
这是一项利莫那班(VICTORIA)试验的通过计算机断层扫描评估内脏脂肪减少的双盲、安慰剂对照亚研究。
67 名年龄在 35-70 岁的腹部肥胖、代谢综合征志愿者在学术医疗中心的一般临床研究中心参加了这项研究。
干预措施包括为期 12 个月的生活方式体重管理计划,加上利莫那班 20mg/d 或安慰剂。
干预前后进行了体成分和两步正葡萄糖、高胰岛素钳夹。胰岛素敏感性通过抑制棕榈酸浓度 [IC50(palmitate)] 的 50%所需的胰岛素浓度来评估,通过棕榈酸 [IC50(palmitate)f] 和肝葡萄糖输出 [IC50(HGO)] 的通量以及胰岛素刺激的葡萄糖摄取(Δ葡萄糖消失量/Δ胰岛素浓度--葡萄糖斜率)。
利莫那班组的体脂减少了 4.5±2.9%(标准差),安慰剂组减少了 1.9±4.5%(P<0.005)。主要[改善 IC50(palmitate) 和 IC50(palmitate)f]和次要[改善 IC50(HGO) 和葡萄糖斜率]结果在利莫那班组和安慰剂组之间没有显著差异。事后分析显示,1)利莫那班组中体重指数(BMI)和 IC50(palmitate)的变化相关(P=0.005);当控制 BMI 下降更多时,这种关系与安慰剂组没有显著差异(P=0.5);2)两组胰岛素调节的葡萄糖摄取都有所改善(P=0.002),与 BMI 的变化相关。
在人类中,利莫那班治疗观察到的游离脂肪酸和葡萄糖代谢的胰岛素调节改善并不大于单独减肥的预测。