Department of Addictive Behavior and Addiction Medicine, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
JAMA Psychiatry. 2014 Nov;71(11):1254-61. doi: 10.1001/jamapsychiatry.2014.1215.
Obesity has emerged as a leading health threat but its biological basis remains insufficiently known, hampering the search for novel treatments. Here, we study oleoylethanolamide, a naturally occurring lipid that has been clearly implicated in weight regulation in animals. However, its role for weight regulation and obesity in humans is still unclear.
To investigate associations between plasma oleoylethanolamide levels and body mass index (BMI, calculated as weight in kilograms divided by height in meters squared) and functional magnetic resonance imaging response to food stimuli in obese patients and matched control participants.
DESIGN, SETTING, AND PARTICIPANTS: Case-control study of 21 obese patients and 24 matched control participants. Obesity was defined as having a BMI of at least 30. The mean age of participants was 40.8 years and BMIs ranged from 18.2 to 47.5.
Interactions between plasma oleoylethanolamide levels and obesity on BMI and functional magnetic resonance imaging response to food stimuli.
Associations between oleoylethanolamide and BMI differed significantly depending on whether individuals were obese or not (P = .02). In obese individuals, oleoylethanolamide showed a trend toward a positive correlation with BMI (P = .06, ρ = 0.42), while this relationship was inverse for nonobese control participants (P = .07, ρ = -0.34). Similarly, we found significant interactions between oleoylethanolamide levels and obesity on food-related brain activation in cortical areas associated with reward processing and interoceptive signaling (P = .009). Specifically, nonobese individuals with higher oleoylethanolamide levels had higher insular brain activity (P < .001, ρ = 0.70); again, the relationship trended to be inverse for obese patients (P = .11, ρ = -0.36). These effects were not associated with plasma levels of leptin and anandamide, suggesting an independent role of oleoylethanolamide in hunger-associated interoceptive signaling. Analysis of food craving during the functional magnetic resonance imaging task suggested that the identified brain areas may be involved in suppressing food-liking reactions in nonobese individuals.
This study suggests that oleoylethanolamide-mediated signaling plays an important role for hedonic regulation of food craving and obesity in humans and thus may be a valuable target for developing novel antiobesity drugs.
肥胖已成为主要的健康威胁,但肥胖的生物学基础仍知之甚少,这阻碍了新型治疗方法的研发。本文研究了油酰乙醇酰胺,这是一种天然存在的脂质,在动物体重调节中已被明确涉及。然而,其在人类体重调节和肥胖中的作用仍不清楚。
研究肥胖患者和匹配的对照组参与者血浆油酰乙醇酰胺水平与体重指数(BMI,体重以千克为单位除以身高以米为单位)和对食物刺激的功能性磁共振成像反应之间的关联。
设计、地点和参与者:21 名肥胖患者和 24 名匹配对照组参与者的病例对照研究。肥胖定义为 BMI 至少为 30。参与者的平均年龄为 40.8 岁,BMI 范围为 18.2 至 47.5。
血浆油酰乙醇酰胺水平与肥胖对 BMI 和对食物刺激的功能性磁共振成像反应的相互作用。
油酰乙醇酰胺与 BMI 之间的关联因个体是否肥胖而有显著差异(P=0.02)。在肥胖个体中,油酰乙醇酰胺与 BMI 呈正相关趋势(P=0.06,ρ=0.42),而在非肥胖对照组参与者中,这种关系则相反(P=0.07,ρ=-0.34)。同样,我们发现油酰乙醇酰胺水平与肥胖对与奖励处理和内脏信号相关的皮质区域的食物相关大脑激活之间存在显著相互作用(P=0.009)。具体而言,具有较高油酰乙醇酰胺水平的非肥胖个体的岛叶大脑活动更高(P<0.001,ρ=0.70);同样,这种关系对肥胖患者呈负相关趋势(P=0.11,ρ=-0.36)。这些影响与血浆瘦素和花生四烯酸酰胺水平无关,表明油酰乙醇酰胺在饥饿相关内脏信号中发挥独立作用。对功能性磁共振成像任务中食物渴望的分析表明,所确定的大脑区域可能参与抑制非肥胖个体对食物的喜爱反应。
这项研究表明,油酰乙醇酰胺介导的信号在人类对食物渴望的愉悦调节和肥胖中起着重要作用,因此可能是开发新型抗肥胖药物的有价值的靶点。