Doucette Wilder T, Smedley Elizabeth B, Ruiz-Jaquez Metztli, Khokhar Jibran Y, Smith Kyle S
Department of Psychiatry, Dartmouth Hitchcock Medical Center, Lebanon, NH, United Sates; Geisel School of Medicine, Hanover, NH, United Sates.
Department of Psychological and Brain Sciences, Dartmouth College, Hanover, NH, United Sates; Department of Psychology and Neuroscience Program, Temple University, Philadelphia, PA, United Sates.
Brain Res. 2022 Jun 1;1784:147886. doi: 10.1016/j.brainres.2022.147886. Epub 2022 Mar 18.
Current treatments for obesity do not reliably reduce body weight over time. New interventional strategies, including chemogenetics, carry promise based on preclinical animal studies. Here, we focused on the ventral pallidum (VP) due to its clearly established role in eating behavior. Chronic inhibitory or excitatory chemogenetic activation was used to modulate the activity of VP-targeted neurons in rats on an obesogenic diet. Based on studies using acute VP manipulations, we hypothesized that VP inhibition would decrease weight gain, while VP stimulation would increase weight. Instead, both manipulations caused weight gain over time, and in a manner not clearly linked to consumption levels. We theorize that the complex reciprocal feedback between ventral striatal structures and metabolic centers likely underpin our unexpected findings. Regardless, this study suggests that the result of strategies to prevent obesity with chronic neuromodulation could be difficult to predict from prior preclinical studies that have used acute interventions.
目前针对肥胖症的治疗方法并不能长期可靠地减轻体重。包括化学遗传学在内的新干预策略,基于临床前动物研究展现出了前景。在此,我们将重点放在腹侧苍白球(VP)上,因为其在进食行为中所起的作用已明确确立。慢性抑制性或兴奋性化学遗传激活被用于调节食用致肥胖饮食的大鼠中靶向VP的神经元的活性。基于使用急性VP操纵的研究,我们假设抑制VP会减少体重增加,而刺激VP会增加体重。相反,随着时间的推移,两种操纵都导致了体重增加,而且其方式与消费水平并无明显关联。我们推测腹侧纹状体结构与代谢中心之间复杂的相互反馈可能是我们意外发现的基础。无论如何,这项研究表明,从先前使用急性干预的临床前研究中很难预测慢性神经调节预防肥胖症策略的结果。