The gut hormone Allatostatin C/Somatostatin regulates food intake and metabolic homeostasis under nutrient stress
Olga Kubrak,
Takashi Koyama,
Nadja Ahrentløv,
Line Jensen,
Alina Malita,
Muhammad T. Naseem,
Mette Lassen,
Stanislav Nagy,
Michael J. Texada,
Kenneth V. Halberg and
Kim Rewitz ()
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Olga Kubrak: University of Copenhagen
Takashi Koyama: University of Copenhagen
Nadja Ahrentløv: University of Copenhagen
Line Jensen: University of Copenhagen
Alina Malita: University of Copenhagen
Muhammad T. Naseem: University of Copenhagen
Mette Lassen: University of Copenhagen
Stanislav Nagy: University of Copenhagen
Michael J. Texada: University of Copenhagen
Kenneth V. Halberg: University of Copenhagen
Kim Rewitz: University of Copenhagen
Nature Communications, 2022, vol. 13, issue 1, 1-17
Abstract:
Abstract The intestine is a central regulator of metabolic homeostasis. Dietary inputs are absorbed through the gut, which senses their nutritional value and relays hormonal information to other organs to coordinate systemic energy balance. However, the gut-derived hormones affecting metabolic and behavioral responses are poorly defined. Here we show that the endocrine cells of the Drosophila gut sense nutrient stress through a mechanism that involves the TOR pathway and in response secrete the peptide hormone allatostatin C, a Drosophila somatostatin homolog. Gut-derived allatostatin C induces secretion of glucagon-like adipokinetic hormone to coordinate food intake and energy mobilization. Loss of gut Allatostatin C or its receptor in the adipokinetic-hormone-producing cells impairs lipid and sugar mobilization during fasting, leading to hypoglycemia. Our findings illustrate a nutrient-responsive endocrine mechanism that maintains energy homeostasis under nutrient-stress conditions, a function that is essential to health and whose failure can lead to metabolic disorders.
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-28268-x
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DOI: 10.1038/s41467-022-28268-x
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