Estrogen-related receptor [beta] deficiency alters body composition and response to restraint stress

• Published in: BMC physiology Vol. 13
• Main Authors: Byerly, Mardi S, Swanson, Roy D, Wong, G William, Blackshaw, Seth
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 22.09.2013; BioMed Central
• Subjects: ACTH; Analysis; Binding sites; Brain; Corticosterone; Corticotropin releasing hormone; Deoxyribonucleic acid; DNA; DNA binding proteins; Drug dosages; Estrogen; Estrogens; Gene expression; Genetic aspects; Genetic transcription; Ligands; Medicine; Metabolism; Neuropeptide Y; Neuropeptides; Phenols; Physiological aspects; Receptors; Rodents; Stress
• ISSN: 1472-6793; 1472-6793
• DOI: 10.1186/1472-6793-13-10

Estrogen-related receptors (ERRs) are orphan nuclear hormone receptors expressed in metabolically active tissues and modulate numerous homeostatic processes. ERRs do not bind the ligand estrogen, but they are able to bind the estrogen response element (ERE) embedded within the ERR response elements (ERREs) to regulate transcription of genes. Previous work has demonstrated that adult mice lacking Err[beta] have altered metabolism and meal patterns. To further understand the biological role of Err[beta], we characterized the stress response of mice deficient for one or both alleles of Err[beta]. Sox2-Cre:Err[beta] mice lack Err[beta] expression in all tissues of the developing embryo. Sox2-Cre:Err[beta].sup.+/lox heterozygotes were obese, had increased Npy and Agrp gene expression in the arcuate nucleus of the hypothalamus, and secreted more corticosterone in response to stress. In contrast, Sox2-Cre:Err[beta].sup.lox/lox homozygotes were lean and, despite increased Npy and Agrp gene expression, did not secrete more corticosterone in response to stress. Sox2-Cre:Err[beta].sup.+/lox and Sox2-Cre:Err[beta].sup.lox/lox mice treated with the Err[beta] and Err[gamma] agonist DY131 demonstrated increased corticotropin-releasing hormone (Crh) expression in the paraventricular nucleus of the hypothalamus, although corticosterone levels were not affected. Nes-Cre:Err[beta].sup.lox/lox mice, which selectively lack Err[beta] expression in the nervous system, also demonstrated elevated stress response during an acoustic startle response test and decreased expression of both Crh and corticotropin-releasing hormone receptor 2 (Crhr2). Loss of Err[beta] affects body composition, neuropeptide levels, stress hormones, and centrally-modulated startle responses of mice. These results indicate that Err[beta] alters the function of the hypothalamic-pituitary-adrenocortical axis and indicates a role for Err[beta] in regulating stress response.