Journal Article

Activation of the hypothalamic–pituitary–adrenal axis by exogenous and endogenous GDF15

Breen, Danna M., Rostron, Anthony J., Rimmington, Debra, Clatworthy, Menna R., Yeo, Giles S. H., Moita, Luís F., Coll, Anthony P., Tadross, John A., Tung, Y. C. Loraine, Bennett, Don, Liu, Hui, Neves-Costa, Ana, Bence, Kendra K., Scott, Jonathan, Melvin, Audrey, Kim, Hanna, Simpson, A. John, Cimino, Irene, O’Rahilly, Stephen, Pedersen, Kent, Jørgensen, Sebastian Beck, Joaquim, Stephanie, Kohnke, Sara N., Lee, E-Chiang, Barker, Peter, Lockhart, Samuel M., Barros, André, Burling, Keith

2021

Overview

An acute increase in the circulating concentration of glucocorticoid hormones is essential for the survival of severe somatic stresses. Circulating concentrations of GDF15, a hormone that acts in the brain to reduce food intake, are frequently elevated in stressful states. We now report that GDF15 potently activates the hypothalamic–pituitary–adrenal (HPA) axis in mice and rats. A blocking antibody to the GDNF-family receptor α-like receptor completely prevented the corticosterone response to GDF15 administration. In wild-type mice exposed to a range of stressful stimuli, circulating levels of both corticosterone and GDF15 rose acutely. In the case of Escherichia coli or lipopolysaccharide injections, the vigorous proinflammatory cytokine response elicited was sufficient to produce a near-maximal HPA response, regardless of the presence or absence of GDF15. In contrast, the activation of the HPA axis seen in wild-type mice in response to the administration of genotoxic or endoplasmic reticulum toxins, which do not provoke a marked rise in cytokines, was absent in Gdf15 −/− mice. In conclusion, consistent with its proposed role as a sentinel hormone, endogenous GDF15 is required for the activation of the protective HPA response to toxins that do not induce a substantial cytokine response. In the context of efforts to develop GDF15 as an antiobesity therapeutic, these findings identify a biomarker of target engagement and a previously unrecognized pharmacodynamic effect, which will require monitoring in human studies.

• Publisher: National Academy of Sciences
• Subject: Animals / Antibodies / Biological Sciences / Biomarkers / Blocking antibodies / Cisplatin - administration & dosage / Cisplatin - pharmacology / Corticosterone / Cytokines / E coli / Endoplasmic reticulum / Endoplasmic Reticulum Stress - drug effects / Food intake / Genotoxicity / Glial cell line-derived neurotrophic factor / Glial Cell Line-Derived Neurotrophic Factor Receptors - metabolism / Glucocorticoids / Glucocorticoids - metabolism / Growth Differentiation Factor 15 - administration & dosage / Growth Differentiation Factor 15 - metabolism / Hormones / Humans / Hypothalamic-pituitary-adrenal axis / Hypothalamo-Hypophyseal System - metabolism / Hypothalamus / Inflammation / Lipopolysaccharides / Mice / Pharmacodynamics / Physiology / Pituitary / Pituitary-Adrenal System - metabolism / Rats / Receptors / Target recognition / Toxins / Tunicamycin - pharmacology