Department of Molecular Genetics and Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390-8584, USA.
Cell. 2013 Dec 5;155(6):1323-36. doi: 10.1016/j.cell.2013.10.052.
Circulating glucocorticoid levels oscillate with a robust circadian rhythm, yet the physiological relevance of this rhythmicity remains unclear. Here, we show that modulation of circadian glucocorticoid oscillation by enhancing its amplitude leads to anxiolytic-like behavior. We observed that mice with adrenal subcapsular cell hyperplasia (SCH), a common histological change in the adrenals, are less anxious than mice without SCH. This behavioral change was found to be dependent on the higher amplitude of glucocorticoid oscillation, although the total glucocorticoid secretion is not increased in these mice. Genetic and pharmacologic experiments demonstrated that intermediate opioid peptides secreted from SCH activate CXCR7, a β-arrestin-biased G-protein-coupled receptor (GPCR), to augment circadian oscillation of glucocorticoid levels in a paracrine manner. Furthermore, recapitulating this paracrine axis by subcutaneous administration of a synthetic CXCR7 ligand is sufficient to induce anxiolytic-like behavior. Adrenocortical β-arrestin-biased GPCR signaling is a potential target for modulating circadian glucocorticoid oscillation and emotional behavior.
循环糖皮质激素水平随强大的昼夜节律而波动,但这种节律的生理相关性尚不清楚。在这里,我们表明通过增强其幅度来调节昼夜节律糖皮质激素的波动会导致类似焦虑的行为。我们观察到,具有肾上腺包膜下细胞增生(SCH)的小鼠,即肾上腺的一种常见组织学变化,比没有 SCH 的小鼠焦虑程度更低。这种行为变化被发现依赖于糖皮质激素波动的更高幅度,尽管这些小鼠中的总糖皮质激素分泌没有增加。遗传和药理学实验表明,SCH 分泌的中间阿片肽激活 CXCR7,一种β-arrestin 偏向的 G 蛋白偶联受体(GPCR),以旁分泌方式增强糖皮质激素水平的昼夜节律波动。此外,通过皮下给予合成的 CXCR7 配体来再现这种旁分泌轴足以诱导类似焦虑的行为。肾上腺皮质β-arrestin 偏向的 GPCR 信号是调节昼夜节律糖皮质激素波动和情绪行为的潜在靶点。