# Rapid hormonal modulation of feeding circuit dynamics and its disruption in obesity

> **NIH NIH R01** · NORTHWESTERN UNIVERSITY · 2021 · $374,138

## Abstract

PROJECT SUMMARY
Obesity is a staggering public health threat associated with dysregulation of both long-acting homeostatic
feedback that modulates metabolism and satiety, and fast acting signals from the gut driving meal termination.
Excessive consumption of highly processed foods rich in sugar is increasingly implicated in the development of
obesity and its comorbidities. A major gap in our knowledge is to understand how carbohydrate-rich diets
modulate satiation via rapid gut-brain communication in normal weight and obese animals. Using a model I
pioneered to dissect the effects of gastrointestinal nutrient delivery on the in vivo dynamics of hypothalamic
feeding circuits, I previously showed that gastric infusion of macronutrients rapidly inhibits a population of hunger-
promoting neurons in the hypothalamus known as AgRP neurons. This inhibition is proportional to the total
number of calories infused and independent of macronutrient identity, though the molecular mechanisms are
macronutrient specific. More recent data show that obesity induced by a high-fat diet (HFD) results in a selective
decrease in fat-mediated AgRP neuron inhibition, supporting the idea that over-nutrition induces nutrient-specific
changes along the gut-brain axis. However, the molecular mechanisms of AgRP neuron inhibition induced by
carbohydrate ingestion remain largely unknown.
The work proposed here will test several hypotheses to begin addressing this question. Aim 1 uses a combination
of pharmacologic and conditional genetic tools to define a role for rapid post-ingestive hormone release from a
specialized population of gastrointestinal tract-lining cells known as enteroendocrine cells (EECs) in driving
carbohydrate-mediated AgRP neuron inhibition. In addition to defining the specific secreted signals required for
glucose-induced gut-brain communication, we will determine in which tissues and cell types these hormones act
to elicit changes in neural activity. In Aim 2, based upon our results in mice fed a HFD, we will test the hypothesis
that obesity induced by high-carbohydrate diets results in unique changes in the dynamics of gut-brain
communication compared to HFD due to nutrient-specific changes in the transcriptional landscape of EECs.
These studies will close several gaps in our understanding of how carbohydrate intake rapidly modulates feeding
circuit activity. It will clarify the role of key glucose-released gut hormones in mediating these dynamics,
demonstrate where critical hormone signaling is required, and reveal how carbohydrate overconsumption
changes the gut-brain axis at the levels of both neural activity and EEC function. Collectively, the integration of
these data will significantly advance our understanding of how over-nutrition leads to nutrient-specific changes
in critical homeostatic processes. This will ultimately yield novel insights into the treatment and prevention of
obesity.

## Key facts

- **NIH application ID:** 10182404
- **Project number:** 1R01DK128477-01
- **Recipient organization:** NORTHWESTERN UNIVERSITY
- **Principal Investigator:** Lisa R Beutler
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $374,138
- **Award type:** 1
- **Project period:** 2021-04-01 → 2026-01-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10182404

## Citation

> US National Institutes of Health, RePORTER application 10182404, Rapid hormonal modulation of feeding circuit dynamics and its disruption in obesity (1R01DK128477-01). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10182404. Licensed CC0.

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