Search Results
Search for other papers by Madeleine R Di Natale in
Google Scholar
PubMed
Search for other papers by Alita Soch in
Google Scholar
PubMed
Search for other papers by Ilvana Ziko in
Google Scholar
PubMed
Search for other papers by Simone N De Luca in
Google Scholar
PubMed
Search for other papers by Sarah J Spencer in
Google Scholar
PubMed
Search for other papers by Luba Sominsky in
Google Scholar
PubMed
Introduction Psychological stress has well-known inhibitory effects on reproductive function ( Rivier & Rivest 1991 , Tilbrook et al. 2002 , Young et al. 2006 , Lynch et al. 2014 ), suppressing hypothalamic–pituitary–gonadal (HPG
Search for other papers by Ladan Eshkevari in
Google Scholar
PubMed
Search for other papers by Eva Permaul in
Google Scholar
PubMed
Search for other papers by Susan E Mulroney in
Google Scholar
PubMed
Introduction The classic response to chronic stress consists of an elegant, concerted interplay of two important pathways, the sympathetic nervous system (SNS) and the hypothalamus–pituitary–adrenal axis (HPA). The chronic activation of these stress
Search for other papers by V Squicciarini in
Google Scholar
PubMed
Search for other papers by R Riquelme in
Google Scholar
PubMed
Search for other papers by K Wilsterman in
Google Scholar
PubMed
Helen Wills Neuroscience Institute, UC Berkeley, Berkeley, California, USA
Search for other papers by G E Bentley in
Google Scholar
PubMed
Search for other papers by H E Lara in
Google Scholar
PubMed
) from sympathetic nerve terminals ( Benedict et al . 1979 ). Based on this observation, we have established a rat PCOS model, which involves chronic exposure to a cold sympathetic stress stimulus ( Bhatnagar et al . 1995 , Dorfman et al . 2003
Search for other papers by Raul Riquelme in
Google Scholar
PubMed
Search for other papers by Freddy Ruz in
Google Scholar
PubMed
Search for other papers by Artur Mayerhofer in
Google Scholar
PubMed
Search for other papers by Hernán E Lara in
Google Scholar
PubMed
and are associated with deregulation of ovarian function in pathologies such as polycystic ovary syndrome (PCOS). Exposure of adult rats to cold stress increases sympathetic activity and NA levels in the ovary ( Dorfman et al. 2003 , Bernuci et
Search for other papers by Henrik Oster in
Google Scholar
PubMed
promote the availability of energy at times of need while minimizing overall energetic needs at other times. Two of these, the stress system and the circadian clock, work closely together for this goal, but use fundamentally different principles of
Search for other papers by Barry N Madison in
Google Scholar
PubMed
Search for other papers by Patrick T K Woo in
Google Scholar
PubMed
Search for other papers by Nicholas J Bernier in
Google Scholar
PubMed
Introduction Challenges that disturb the homoeostasis of an animal can be met by an activation of the stress response. A key component of this response in fish involves the stimulation of the hypothalamic–pituitary–interrenal (HPI) axis
Search for other papers by Patricia Joseph-Bravo in
Google Scholar
PubMed
Search for other papers by Lorraine Jaimes-Hoy in
Google Scholar
PubMed
Search for other papers by Jean-Louis Charli in
Google Scholar
PubMed
biosynthesis studies Before continuing with this review we would like to stress some problems worthy of consideration when studying the regulation of TRH biosynthesis, given the diversity of experimental paradigms used. Cell lines are homogenous but with a
Search for other papers by George Fink in
Google Scholar
PubMed
secretion of pituitary ‘thyrotropic and adrenotropic principles’. Selye’s observations translate in modern terms to stress-induced immunosuppression, peptic ulceration and inflammatory bowel disease (IBD) and activation of the two main vertebrate stress
Search for other papers by Kook Hwan Kim in
Google Scholar
PubMed
Severance Biomedical Research Institute, Department of Internal Medicine, Yonsei University College of Medicine, 50 Yonsei‐ro, Seodaemun‐gu, Seoul 120-752, Korea
Search for other papers by Myung-Shik Lee in
Google Scholar
PubMed
of the beneficial metabolic effects of several therapeutic agents ( Fig. 1 ). Figure 1 Functional role of fibroblast growth factor 21 (FGF21) secreted from multiple organs in response to diverse stresses or stimuli. FGF21 expression is induced in
Search for other papers by M J F Newson in
Google Scholar
PubMed
Search for other papers by G R Pope in
Google Scholar
PubMed
Search for other papers by E M Roberts in
Google Scholar
PubMed
Search for other papers by S J Lolait in
Google Scholar
PubMed
Search for other papers by A-M O'Carroll in
Google Scholar
PubMed
multiple homeostatic perturbations. These include regulation of fluid ( O'Carroll & Lolait 2003 ) and cardiovascular homeostasis ( Ishida et al . 2004 ), the stress response ( O'Carroll et al . 2003 ), food intake ( Taheri et al . 2002 ), gastric cell