Division of Medical Sciences & Graduate Entry Medicine, School of Medicine, Faculty of Medicine & Health Sciences, University of Nottingham, Royal Derby Hospital Centre, Uttoxeter Road, Derby, DE22 3DT, UK.
Lipids Health Dis. 2014 Mar 4;13:43. doi: 10.1186/1476-511X-13-43.
Circulating endocannabinoid levels are increased in obesity and diabetes. We have shown that fatty acid amide hydrolase (FAAH, an endocannabinoid hydrolysing enzyme) in subcutaneous adipose tissue positively correlates with BMI in healthy volunteers. The aim of the present study was to investigate whether the hydrolytic enzymes of the endocannabinoid system are affected by diabetes or metabolic syndrome in obesity.
Using radiolabelled substrates, FAAH and monoacylglycerol lipase (MGL) activities were assessed in adipocytes from various adipose depots in Zucker rats (n = 22, subcutaneous abdominal, visceral and epididymal) and bariatric patients (n = 28, subcutaneous abdominal and omental).
FAAH activity was significantly increased in adipocytes of obese (Zucker Fatty) compared to Zucker lean rats (P < 0.05) but was not raised in the Zucker Diabetic Fatty rats (ZDF). MGL activity was raised in both Zucker Fatty (P < 0.001-0.01) and ZDF rats (P < 0.05) and was positively correlated with body weight and plasma glucose levels (P < 0.01). In bariatric patients (BMI range 37-58 kg.m²), there was a trend for MGL activity to correlate positively with BMI, reaching significance when type 2 diabetic patients were removed. FAAH and MGL activities in obese humans were not correlated with blood pressure, skinfold thicknesses, fasting glucose, insulin, HbA1c, triglycerides or cholesterol levels.
FAAH in adipocytes is differentially altered in animal models of obesity and diabetes, while MGL activity is increased by both. However, in obese humans, FAAH or MGL activity in adipocytes is not affected by diabetes, dyslipidaemia or other markers of metabolic dysfunction. This suggests increased circulating levels of endocannabinoids are not a result of altered degradation in adipose tissue.
循环内源性大麻素水平在肥胖和糖尿病中升高。我们已经表明,在健康志愿者中,皮下脂肪组织中的脂肪酸酰胺水解酶(FAAH,一种内源性大麻素水解酶)与 BMI 呈正相关。本研究的目的是研究肥胖中糖尿病或代谢综合征是否会影响内源性大麻素系统的水解酶。
使用放射性标记的底物,评估 Zucker 大鼠(n=22,皮下腹部、内脏和附睾)和肥胖症患者(n=28,皮下腹部和网膜)不同脂肪组织中的脂肪细胞中的 FAAH 和单酰基甘油脂肪酶(MGL)活性。
与 Zucker 瘦鼠相比,肥胖(Zucker 肥胖)大鼠的脂肪细胞中 FAAH 活性显著升高(P<0.05),但在 Zucker 糖尿病肥胖(ZDF)大鼠中并未升高。MGL 活性在 Zucker 肥胖(P<0.001-0.01)和 ZDF 大鼠中均升高(P<0.05),并且与体重和血浆葡萄糖水平呈正相关(P<0.01)。在肥胖症患者(BMI 范围 37-58kg.m²)中,MGL 活性与 BMI 呈正相关趋势,当排除 2 型糖尿病患者时,该趋势具有统计学意义。肥胖人群的 FAAH 和 MGL 活性与血压、皮褶厚度、空腹血糖、胰岛素、HbA1c、甘油三酯或胆固醇水平无关。
肥胖动物模型中脂肪细胞中的 FAAH 发生了不同的改变,而糖尿病则会增加 MGL 活性。然而,在肥胖人群中,脂肪细胞中的 FAAH 或 MGL 活性不受糖尿病、血脂异常或其他代谢功能障碍标志物的影响。这表明循环内源性大麻素水平升高不是由于脂肪组织降解改变所致。