A new model for the HPA axis explains dysregulation of stress hormones on the timescale of weeks

被引:111
作者
Karin, Omer [1 ]
Raz, Moriya [1 ]
Tendler, Avichai [1 ]
Bar, Alon [1 ]
Kohanim, Yael Korem [1 ]
Milo, Tomer [1 ]
Alon, Uri [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, Rehovot, Israel
基金
欧洲研究理事会;
关键词
dynamical compensation; exact adaptation; endocrine circuits; mathematical models of disease; systems medicine; CORTICOTROPIN-RELEASING HORMONE; ADRENAL-GLAND VOLUME; AUTOADDICTION OPIOID MODEL; BETA-ENDORPHIN; GLUCOCORTICOID-RECEPTOR; MAJOR DEPRESSION; CUSHINGS-SYNDROME; MATHEMATICAL-MODEL; CORTISOL RESPONSE; HUMAN CRH;
D O I
10.15252/msb.20209510
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stress activates a complex network of hormones known as the hypothalamic-pituitary-adrenal (HPA) axis. The HPA axis is dysregulated in chronic stress and psychiatric disorders, but the origin of this dysregulation is unclear and cannot be explained by current HPA models. To address this, we developed a mathematical model for the HPA axis that incorporates changes in the total functional mass of the HPA hormone-secreting glands. The mass changes are caused by HPA hormones which act as growth factors for the glands in the axis. We find that the HPA axis shows the property of dynamical compensation, where gland masses adjust over weeks to buffer variation in physiological parameters. These mass changes explain the experimental findings on dysregulation of cortisol and ACTH dynamics in alcoholism, anorexia, and postpartum. Dysregulation occurs for a wide range of parameters and is exacerbated by impaired glucocorticoid receptor (GR) feedback, providing an explanation for the implication of GR in mood disorders. These findings suggest that gland-mass dynamics may play an important role in the pathophysiology of stress-related disorders.
引用
收藏
页数:13
相关论文
共 97 条
[91]   Origin of ultradian pulsatility in the hypothalamic-pituitary-adrenal axis [J].
Walker, Jamie J. ;
Terry, John R. ;
Lightman, Stafford L. .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2010, 277 (1688) :1627-1633
[92]   Glucocorticoid receptor gene (NR3C1) DNA methylation in association with trauma, psychopathology, transcript expression, or genotypic variation: A systematic review [J].
Watkeys, Oliver J. ;
Kremerskothen, Kyle ;
Quide, Yann ;
Fullerton, Janice M. ;
Green, Melissa J. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2018, 95 :85-122
[93]   Epigenetic programming by maternal behavior [J].
Weaver, ICG ;
Cervoni, N ;
Champagne, FA ;
D'Alessio, AC ;
Sharma, S ;
Seckl, JR ;
Dymov, S ;
Szyf, M ;
Meaney, MJ .
NATURE NEUROSCIENCE, 2004, 7 (08) :847-854
[94]   Regional specificity of brain gluclocorticoid receptor mRNA alterations in subjects with schizophrenia and mood disorders [J].
Webster, MJ ;
Knable, MB ;
O'Grady, J ;
Orthmann, J ;
Weickert, CS .
MOLECULAR PSYCHIATRY, 2002, 7 (09) :985-994
[95]   QUANTIFICATION OF MORPHOLOGICAL-CHANGES IN PITUITARY CORTICOTROPES PRODUCED BY INVIVO CORTICOTROPIN-RELEASING FACTOR STIMULATION AND ADRENALECTOMY [J].
WESTLUND, KN ;
AGUILERA, G ;
CHILDS, GV .
ENDOCRINOLOGY, 1985, 116 (01) :439-445
[96]   CHANGES IN RELEASABILITY OF ACTH AND BETA-ENDORPHIN WITH CHRONIC STRESS [J].
YOUNG, E ;
AKIL, H .
NEUROPEPTIDES, 1985, 5 (4-6) :545-548
[97]   Mathematical Modelling of Endocrine Systems [J].
Zavala, Eder ;
Wedgwood, Kyle C. A. ;
Voliotis, Margaritis ;
Tabak, Joel ;
Spiga, Francesca ;
Lightman, Stafford L. ;
Tsaneva-Atanasova, Krasimira .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2019, 30 (04) :244-257