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腹侧被盖区神经降压素受体-1 神经元的激活可促进体重减轻。

Activation of ventral tegmental area neurotensin Receptor-1 neurons promotes weight loss.

机构信息

Neuroscience Graduate Program, Michigan State University, East Lansing, MI, 48114, USA; Department of Pharmacology and Toxicology, East Lansing, MI, 48114, USA.

Neuroscience Graduate Program, Michigan State University, East Lansing, MI, 48114, USA.

出版信息

Neuropharmacology. 2021 Sep 1;195:108639. doi: 10.1016/j.neuropharm.2021.108639. Epub 2021 Jun 9.

Abstract

Dopamine (DA) neurons in the ventral tegmental area (VTA) modulate physical activity and feeding behaviors that are disrupted in obesity. Yet, the heterogeneity of VTA DA neurons has hindered determination of which ones might be leveraged to support weight loss. We hypothesized that increased activity in the subset of VTA DA neurons expressing neurotensin receptor-1 (NtsR1) might promote weight loss behaviors. To test this, we used Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) to activate VTA NtsR1 neurons in normal weight and diet-induced obese mice. Acute activation of VTA NtsR1 neurons (24hr) significantly decreased body weight in normal weight and obese mice by reducing food intake and increasing physical activity. Moreover, daily activation of VTA NtsR1 neurons in obese mice sustained weight loss over 7 days. Activating VTA NtsR1 neurons also suppressed how much mice worked to obtain sucrose rewards, even when there was high motivation to consume. However, VTA NtsR1 neural activation was not reinforcing, nor did it invoke liabilities associated with whole-body NtsR1 agonism such as anxiety, vasodepressor response or hypothermia. Activating VTA NtsR1 neurons therefore promotes dual behaviors that support weight loss without causing adverse effects, and is worth further exploration for managing obesity.

摘要

腹侧被盖区(VTA)中的多巴胺(DA)神经元调节身体活动和摄食行为,而肥胖会破坏这些行为。然而,VTA DA 神经元的异质性阻碍了确定哪些神经元可能被利用来支持体重减轻。我们假设,表达神经降压素受体-1(NtsR1)的 VTA DA 神经元亚群的活性增加可能会促进体重减轻行为。为了验证这一点,我们使用 Designer Receptors Exclusively Activated by Designer Drugs(DREADDs)来激活正常体重和饮食诱导肥胖小鼠的 VTA NtsR1 神经元。急性激活 VTA NtsR1 神经元(24 小时)通过减少食物摄入和增加身体活动,显著降低了正常体重和肥胖小鼠的体重。此外,肥胖小鼠 VTA NtsR1 神经元的每日激活可在 7 天内持续减轻体重。激活 VTA NtsR1 神经元还抑制了老鼠获得蔗糖奖励所需的工作量,即使它们有强烈的消费动机。然而,VTA NtsR1 神经元的激活并没有增强作用,也没有引起全身 NtsR1 激动剂相关的不良反应,如焦虑、血管舒张反应或体温过低。因此,激活 VTA NtsR1 神经元可促进支持体重减轻的双重行为,而不会引起不良反应,值得进一步探索用于肥胖症的治疗。

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