# Neural Mechanism of Impaired Satiation After Magel2 Mutation

> **NIH NIH R21** · UNIVERSITY OF ARIZONA · 2024 · $223,446

## Abstract

Project summary
Satiation is an important aspect of interoception that translates gut signals, such as cholecystokinin (CCK), into
eating suppression. Insatiable appetite is associated with developmental genetic diseases including Prader-Willi
Syndrome (PWS) and Shafer-Young Syndrome (SYS). Paradoxically, individuals with PWS have higher levels
of plasma CCK but consume more food, suggesting that the neural mechanism responsible for detecting
satiation signals is impaired and cannot convert satiation information into eating suppression. However, how the
neural circuit that regulates satiation is impaired in these diseases is still unknown. PWS and SYS share a
common mutation in the Magel2 gene, suggesting that the mutation of this gene might impair the satiation circuit.
Consistent with this, our preliminary results indicate that CCK fails to suppress food intake in Magel2-null mice.
Our previous studies have identified a specific population of neurons in the central nucleus of the amygdala (CeA)
marked by the expression of protein kinase C-delta, which plays a critical role in detecting CCK. Silencing these
neurons prevents the eating suppression caused by CCK and activation of these neurons suppresses food intake.
Here, we found that the response of CeA PKC-δ neurons to CCK is reduced in Magel2 null mice. Therefore, we
hypothesize that the neural circuits involving CeA PKC-δ neurons are impaired after Magel2 mutation. In this
proposal, we aim to determine how the CeA PKC-δ neurons are affected by the Magel2 mutation, using recently
developed in vivo calcium imaging and electrophysiology approaches (Aim 1). Because the total number of CeA
PKC-δ neurons is not affected by Magel2-mutation, we will also test the hypothesis that activation of CeA PKC-
δ neurons suppresses appetite in Magel2-null mice (Aim 2). Successful completion of the proposed studies will
help us understand how satiation and appetite are regulated in the brains of individuals with PWS and SYS.
Additionally, it may suggest novel druggable targets in the brain to control insatiable appetite and obesity in these
diseases, ultimately improving the quality of life.

## Key facts

- **NIH application ID:** 10947972
- **Project number:** 1R21HD116113-01
- **Recipient organization:** UNIVERSITY OF ARIZONA
- **Principal Investigator:** Haijiang Cai
- **Activity code:** R21 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $223,446
- **Award type:** 1
- **Project period:** 2024-09-01 → 2026-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10947972

## Citation

> US National Institutes of Health, RePORTER application 10947972, Neural Mechanism of Impaired Satiation After Magel2 Mutation (1R21HD116113-01). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10947972. Licensed CC0.

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