4.5 Article

Chronic chemogenetic manipulation of ventral pallidum targeted neurons in male rats fed an obesogenic diet

期刊

BRAIN RESEARCH
卷 1784, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.brainres.2022.147886

关键词

Reward; Food; DREADDs; Motivation

资金

  1. Department of Psychiatry at the Geisel School of Medicine at Dartmouth
  2. Dartmouth Clinical and Translational Science Institute from the National Center for Advancing Translational Sciences (NCATS) of the NIH [KL2TR001088]
  3. NIH [1R01DA044199, 1F31DA050369-01]
  4. NSF [IOS1557987]

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Current treatments for obesity have limited effects on long-term weight reduction. Chronic neuromodulation, a new interventional strategy, shows promise based on preclinical animal studies. This study focused on the ventral pallidum (VP) and found that both inhibitory and excitatory chemogenetic manipulations of VP-targeted neurons caused weight gain over time, not clearly related to consumption levels. The complex reciprocal feedback between ventral striatal structures and metabolic centers may underlie these unexpected findings.
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.

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