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Gastric GDF15 levels are regulated by age, sex, and nutritional status in rodents and humans

Pena León, Verónica; Perez Lois, Raquel; Villalón, María; Folgueira Cobos, Cintia; Barja Fernández, Silvia; Prida, Eva; Baltar Boileve, Javier; SANTOS BENITO, FRANCISCO FERNANDO; Fernø, J.; García-Caballero Parada, Tomas; Nogueiras Pozo, Rubén; Quiñones Téllez, María del Mar; AL-MASSADI IGLESIAS, OMAR; Seoane Camino, Luisa Maria
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URI: http://hdl.handle.net/20.500.11940/23241
PMID: 37955834
DOI: 10.1007/s40618-023-02232-y
ESSN: 1720-8386
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J Endocrinol Invest. 2024 May;47(5):1139-1154 (1.785Mb)
VERSIÓN DEL EDITOR (63.29Kb)
Date issued
2024-05
Journal title
Journal of Endocrinological Investigation
Type of content
Artigo
DeCS
adulto | estado nutricional | humanos | animales | ratones | obesidad | mucosa gástrica | ayuno | ratas | factor 15 de diferenciación del crecimiento | características sexuales | estómago
MeSH
Age Factors | Adult | Stomach | Fasting | Humans | Gastric Mucosa | Obesity | Nutritional Status | Male | Sex Factors | Sex Characteristics | Female | Rats | Animals | Growth Differentiation Factor 15 | Mice
Abstract
[EN] Growth differentiation factor 15 (GDF15) is a stress response cytokine that has been proposed as a relevant metabolic hormone. Descriptive studies have shown that plasma GDF15 levels are regulated by short term changes in nutritional status, such as fasting, or in obesity. However, few data exist regarding how GDF15 levels are regulated in peripheral tissues. The aim of the present work was to study the variations on gastric levels of GDF15 and its precursor under different physiological conditions, such as short-term changes in nutritional status or overfeeding achieved by HFD. Moreover, we also address the sex- and age-dependent alterations in GDF15 physiology. The levels of gastric and plasma GDF15 and its precursor were measured in lean and obese mice, rats and humans by western blot, RT-PCR, ELISA, immunohistochemistry and by an in vitro organ culture system. Our results show a robust regulation of gastric GDF15 production by fasting in rodents. In obesity an increase in GDF15 secretion from the stomach is reflected with an increase in circulating levels of GDF15 in rats and humans. Moreover, gastric GDF15 levels increase with age in both rats and humans. Finally, gastric GDF15 levels display sexual dimorphism, which could explain the difference in circulating GFD15 levels between males and females, observed in both humans and rodents. Our results provide clear evidence that gastric GDF15 is a critical contributor of circulating GDF15 levels and can explain some of the metabolic effects induced by GDF15.

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