A high-protein diet-responsive gut hormone regulates behavioral and metabolic optimization in Drosophila melanogaster

Protein is essential for all living organisms; however, excessive protein intake can have adverse effects, such as hyperammonemia. Although mechanisms responding to protein deficiency are well-studied, there is a significant gap in our understanding of how organisms adaptively suppress excessive protein intake. In the present study, utilizing the fruit fly, Drosophila melanogaster, we discover that the peptide hormone CCHamide1 (CCHa1), secreted by enteroendocrine cells in response to a high-protein diet (HPD), is vital for suppressing overconsumption of protein. Gut-derived CCHa1 is received by a small subset of enteric neurons that produce short neuropeptide F, thereby modulating protein-specific satiety. Importantly, impairment of the CCHa1-mediated gut-enteric neuronal axis results in ammonia accumulation and a shortened lifespan under HPD conditions. Collectively, our findings unravel the crosstalk of gut hormone and neuronal pathways that orchestrate physiological responses to prevent and adapt to dietary protein overload.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2024-12-30
DOI
https://doi.org/10.1038/s41467-024-55050-y
Citations
22
Primary Topic
Aquaculture Nutrition and Growth
Type
article
Field-Weighted Citation Impact
13.16

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A high-protein diet-responsive gut hormone regulates behavioral and metabolic optimization in Drosophila melanogaster

Hiromu Tanimoto, Makoto Matsuyama, Shu Kondo, Takashi Nishimura et al.
22 citations
Nature Communications
Aquaculture Nutrition and Growth
13.16
article

A high-protein diet-responsive gut hormone regulates behavioral and metabolic optimization in Drosophila melanogaster

Hiromu Tanimoto, Makoto Matsuyama, Shu Kondo, Takashi Nishimura, Taishi Yoshii, Yuto Yoshinari, Ryusuke Niwa, Tomoe Kobayashi
article en
22 citations

Abstract

Protein is essential for all living organisms; however, excessive protein intake can have adverse effects, such as hyperammonemia. Although mechanisms responding to protein deficiency are well-studied, there is a significant gap in our understanding of how organisms adaptively suppress excessive protein intake. In the present study, utilizing the fruit fly, Drosophila melanogaster, we discover that the peptide hormone CCHamide1 (CCHa1), secreted by enteroendocrine cells in response to a high-protein diet (HPD), is vital for suppressing overconsumption of protein. Gut-derived CCHa1 is received by a small subset of enteric neurons that produce short neuropeptide F, thereby modulating protein-specific satiety. Importantly, impairment of the CCHa1-mediated gut-enteric neuronal axis results in ammonia accumulation and a shortened lifespan under HPD conditions. Collectively, our findings unravel the crosstalk of gut hormone and neuronal pathways that orchestrate physiological responses to prevent and adapt to dietary protein overload.

Nature CommunicationsVol. 15(1)
National Institute of Genetics (JP), University of Tsukuba (JP), Tokyo University of Science (JP), Okayama University (JP), Gunma University (JP), Tohoku University (JP), Shigei Medical Research Institute (JP)
Japan Agency for Medical Research and Development, University of Tsukuba, Japan Society for the Promotion of Science, Life Science Center for Survival Dynamics Tsukuba Advanced Research Alliance, Institute of Genetics, Core Research for Evolutional Science and Technology
Zero hunger
Openalex Percentile: Top 1%
Aquaculture Nutrition and Growth
13.16
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.