Obesity causes selective and long-lasting desensitization of AgRP neurons to dietary fat.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32720646.
- Also identified by DOI 10.7554/eLife.55909 and PMC identifier 7398661.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Body weight is regulated by interoceptive neural circuits that track energy need, but how the activity of these circuits is altered in obesity remains poorly understood. Here we describe the in vivo dynamics of hunger-promoting AgRP neurons during the development of diet-induced obesity in mice. We show that high-fat diet attenuates the response of AgRP neurons to an array of nutritionally-relevant stimuli including food cues, intragastric nutrients, cholecystokinin and ghrelin. These alterations are specific to dietary fat but not carbohydrate or protein. Subsequent weight loss restores the responsiveness of AgRP neurons to exterosensory cues but fails to rescue their sensitivity to gastrointestinal hormones or nutrients. These findings reveal that obesity triggers broad dysregulation of hypothalamic hunger neurons that is incompletely reversed by weight loss and may contribute to the difficulty of maintaining a reduced weight.
Medical subject headings
- Agouti-Related Protein
- Body Weight
- Dietary Fats
- Eating
- Homeostasis
- Hunger
- Obesity