A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila

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A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila. / Malita, Alina; Kubrak, Olga; Koyama, Takashi; Ahrentløv, Nadja; Texada, Michael J.; Nagy, Stanislav; Halberg, Kenneth V.; Rewitz, Kim.

In: Nature Metabolism, Vol. 4, No. 11, 2022, p. 1532-1550.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Malita, A, Kubrak, O, Koyama, T, Ahrentløv, N, Texada, MJ, Nagy, S, Halberg, KV & Rewitz, K 2022, 'A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila', Nature Metabolism, vol. 4, no. 11, pp. 1532-1550. https://doi.org/10.1038/s42255-022-00672-z

APA

Malita, A., Kubrak, O., Koyama, T., Ahrentløv, N., Texada, M. J., Nagy, S., Halberg, K. V., & Rewitz, K. (2022). A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila. Nature Metabolism, 4(11), 1532-1550. https://doi.org/10.1038/s42255-022-00672-z

Vancouver

Malita A, Kubrak O, Koyama T, Ahrentløv N, Texada MJ, Nagy S et al. A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila. Nature Metabolism. 2022;4(11):1532-1550. https://doi.org/10.1038/s42255-022-00672-z

Author

Malita, Alina ; Kubrak, Olga ; Koyama, Takashi ; Ahrentløv, Nadja ; Texada, Michael J. ; Nagy, Stanislav ; Halberg, Kenneth V. ; Rewitz, Kim. / A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila. In: Nature Metabolism. 2022 ; Vol. 4, No. 11. pp. 1532-1550.

Bibtex

@article{a5780eeea13645bf82deeaabe390125b,
title = "A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila",
abstract = "Animals must adapt their dietary choices to meet their nutritional needs. How these needs are detected and translated into nutrient-specific appetites that drive food-choice behaviours is poorly understood. Here we show that enteroendocrine cells of the adult female Drosophila midgut sense nutrients and in response release neuropeptide F (NPF), which is an ortholog of mammalian neuropeptide Y-family gut-brain hormones. Gut-derived NPF acts on glucagon-like adipokinetic hormone (AKH) signalling to induce sugar satiety and increase consumption of protein-rich food, and on adipose tissue to promote storage of ingested nutrients. Suppression of NPF-mediated gut signalling leads to overconsumption of dietary sugar while simultaneously decreasing intake of protein-rich yeast. Furthermore, gut-derived NPF has a female-specific function in promoting consumption of protein-containing food in mated females. Together, our findings suggest that gut NPF-to-AKH signalling modulates specific appetites and regulates food choice to ensure homeostatic consumption of nutrients, providing insight into the hormonal mechanisms that underlie nutrient-specific hungers.",
author = "Alina Malita and Olga Kubrak and Takashi Koyama and Nadja Ahrentl{\o}v and Texada, {Michael J.} and Stanislav Nagy and Halberg, {Kenneth V.} and Kim Rewitz",
note = "Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
doi = "10.1038/s42255-022-00672-z",
language = "English",
volume = "4",
pages = "1532--1550",
journal = "Nature Metabolism",
issn = "2522-5812",
publisher = "Springer",
number = "11",

}

RIS

TY - JOUR

T1 - A gut-derived hormone suppresses sugar appetite and regulates food choice in Drosophila

AU - Malita, Alina

AU - Kubrak, Olga

AU - Koyama, Takashi

AU - Ahrentløv, Nadja

AU - Texada, Michael J.

AU - Nagy, Stanislav

AU - Halberg, Kenneth V.

AU - Rewitz, Kim

N1 - Publisher Copyright: © 2022, The Author(s).

PY - 2022

Y1 - 2022

N2 - Animals must adapt their dietary choices to meet their nutritional needs. How these needs are detected and translated into nutrient-specific appetites that drive food-choice behaviours is poorly understood. Here we show that enteroendocrine cells of the adult female Drosophila midgut sense nutrients and in response release neuropeptide F (NPF), which is an ortholog of mammalian neuropeptide Y-family gut-brain hormones. Gut-derived NPF acts on glucagon-like adipokinetic hormone (AKH) signalling to induce sugar satiety and increase consumption of protein-rich food, and on adipose tissue to promote storage of ingested nutrients. Suppression of NPF-mediated gut signalling leads to overconsumption of dietary sugar while simultaneously decreasing intake of protein-rich yeast. Furthermore, gut-derived NPF has a female-specific function in promoting consumption of protein-containing food in mated females. Together, our findings suggest that gut NPF-to-AKH signalling modulates specific appetites and regulates food choice to ensure homeostatic consumption of nutrients, providing insight into the hormonal mechanisms that underlie nutrient-specific hungers.

AB - Animals must adapt their dietary choices to meet their nutritional needs. How these needs are detected and translated into nutrient-specific appetites that drive food-choice behaviours is poorly understood. Here we show that enteroendocrine cells of the adult female Drosophila midgut sense nutrients and in response release neuropeptide F (NPF), which is an ortholog of mammalian neuropeptide Y-family gut-brain hormones. Gut-derived NPF acts on glucagon-like adipokinetic hormone (AKH) signalling to induce sugar satiety and increase consumption of protein-rich food, and on adipose tissue to promote storage of ingested nutrients. Suppression of NPF-mediated gut signalling leads to overconsumption of dietary sugar while simultaneously decreasing intake of protein-rich yeast. Furthermore, gut-derived NPF has a female-specific function in promoting consumption of protein-containing food in mated females. Together, our findings suggest that gut NPF-to-AKH signalling modulates specific appetites and regulates food choice to ensure homeostatic consumption of nutrients, providing insight into the hormonal mechanisms that underlie nutrient-specific hungers.

U2 - 10.1038/s42255-022-00672-z

DO - 10.1038/s42255-022-00672-z

M3 - Journal article

C2 - 36344765

AN - SCOPUS:85141428212

VL - 4

SP - 1532

EP - 1550

JO - Nature Metabolism

JF - Nature Metabolism

SN - 2522-5812

IS - 11

ER -

ID: 327388275