Evidence map›Paper›PMID 42741020›Full record

ArticleFrontiers in endocrinology2026

Overexpression of FGFR1 in AgRP neurons protects against obesity and improves glucose homeostasis.

Daniel Shookster, Ahjanelle Martin, Madison Gunn, Shea O'Connell, Hu Huang

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Daniel ShooksterEast Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States.
Ahjanelle MartinEast Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States.
Madison GunnEast Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States.
Shea O'ConnellEast Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States.
Hu HuangEast Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, United States.

Funding

FGFR1 Signaling in AgRP Neurons for Regulating MetabolismR15DK139539 · NIDDK · EAST CAROLINA UNIVERSITY · PI HUANG, HU · 2025 to 2025
$453k
The central role of alpha-klotho in regulation of metabolismR15DK121215 · NIDDK · EAST CAROLINA UNIVERSITY · PI HUANG, HU · 2019 to 2019
$443k
NIDDK NIH HHS R15 DK121215NIDDK NIH HHS R15 DK139539
6 · The paper itself

Abstract

Background: The rising prevalence of metabolic disorders highlights the need to identify targetable pathways. Although hypothalamic AgRP neuron signaling influences energy balance, the beneficial role of fibroblast growth factor receptor 1 (FGFR1) within these neurons remains incompletely understood. Methods: We employed an AAV-mediated CRISPR/Cas9 activation system to achieve AgRP neuron-specific overexpression of FGFR1 in adult mice. Metabolic phenotypes were assessed during high-fat diet (HFD) feeding, and mechanistic insights were gained using GT1-7 hypothalamic cells. Results: FGFR1 overexpression in AgRP neurons attenuated high-fat diet (HFD)-induced weight gain and improved glucose tolerance, effects that were associated with reduced energy intake. Mechanistically, FGFR1 overexpression correlated with increased FOXO1 phosphorylation and reduced AgRP mRNA expression, suggesting a potential FGFR1-FOXO1 regulatory axis. Conclusion: These findings identify a contributory role for AgRP neuronal FGFR1 signaling in modulating metabolic outcomes under HFD conditions and suggest that this pathway may represent a potential avenue for further investigation in the context of obesity and diabetes.

Indexed as

Agouti-Related ProteinGlucoseHomeostasisNeuronsObesityReceptor, Fibroblast Growth Factor, Type 1AnimalsDiet, High-FatEnergy MetabolismHypothalamusMaleMiceMice, Inbred C57BLSignal TransductionAgouti-Related ProteinAgrp protein, mouseFgfr1 protein, mouseGlucoseReceptor, Fibroblast Growth Factor, Type 1AgRP neuronFGFR1 expressionglucose homeostasismetabolismobesity

Identifiers

PMID42741020
PMCPMC13572110

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.