PET/fMRI显示减肥手术可以逆转肥胖女性纹状体多巴胺能功能障碍。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Marta Lapo Pais, Joana Crisóstomo, Antero Abrunhosa, Miguel Castelo-Branco
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引用次数: 0

摘要

背景:中心机制可能在减肥手术(BS)的成功中发挥作用,BS是难治性肥胖的治疗选择。我们假设纹状体脑区的中枢多巴胺能受体功能是BS成功的关键机制。方法:我们通过横断面研究,研究了通过BS成功减肥(WL)的纹状体脑区中枢多巴胺2型和3型受体(D2/3 R)。使用正电子发射断层扫描(正电子发射断层扫描)绘制48名女性D2/3 R的不可置换结合电位(BPND): 19名成功缓解BS, 12名肥胖(OB), 17名体重正常的对照组。在感兴趣的区域和体素水平上比较组间参数图。我们还利用功能性磁共振成像(fMRI)研究了脑血氧水平依赖(BOLD)对食物含量的反应,以及关键变量如何与D2/3 R结合相关。结果:我们发现OB组和对照组在腹侧纹状体的平均D2/3 R BPND有显著差异(p = 0.042),在纹状体的体素水平上OB组和其他组之间(p = 0.05)显示OB组纹状体的神经激活也明显高于其他组。此外,D2/3 R BPND值与肥胖患者饮食行为的功能失调自我报告测量、对食物线索的激励显著性和高热量食物偏好相关。值得注意的是,纹状体的BOLD反应(Food > Baseline)与腹侧纹状体的D2/3 R结合呈正相关。结论:肥胖的纹状体多巴胺能功能障碍可能会增强对食物线索的显著性,驱动渴望和强迫进食。BS可能逆转肥胖中发现的纹状体分子和功能破坏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PET/fMRI demonstrates that bariatric surgery may reverse striatal dopaminergic dysfunction in women with obesity.

Background: Central mechanisms may play a role in the success of bariatric surgery (BS), the treatment of choice for refractory obesity. We hypothesize that central dopaminergic receptor function in striatal brain regions is a pivotal mechanism in the success of BS.

Methods: We conducted a cross-sectional study to investigate central dopamine type 2 and 3 receptors (D2/3 R) within striatal brain regions in successful weight loss (WL) through BS. Positron Emission Tomography was used to map nondisplaceable binding potential (BPND) of D2/3 R in 48 women: 19 successful responders to BS, 12 with obesity (OB), and 17 normal-weight controls. Parametric maps were compared between-groups in regions of interest and at voxel-level. We also investigated brain blood oxygenation level-dependent (BOLD) responses to food content using functional Magnetic Resonance Imaging (fMRI) and how key variables correlate with D2/3 R binding.

Results: We find mean D2/3 R BPND significant differences between OB and controls in the ventral striatum (p = 0.042) and at voxel-level across striatum between OB and the other groups (p < 0.05). Food content (Food > Non-food, p = 0.05) reveals significantly higher neural activation in striatum also for OB compared to the other groups. Moreover, D2/3 R BPND values correlate with dysfunctional self-report measures of eating behaviors, incentive salience to food cue and high-calorie food preferences in obesity. Notably, BOLD responses (Food > Baseline) in striatum correlate positively with D2/3 R binding in ventral striatum.

Conclusions: Striatal dopaminergic dysfunction in obesity may enhance salience to food cues, driving cravings and compulsive eating. BS may reverse the striatal molecular and functional disruptions found in obesity.

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