Developmental changes in the endocrine stress response in orangutans (Pongo pygmaeus)

2019 ◽  
Vol 189 (6) ◽  
pp. 659-672 ◽  
Author(s):  
Rafaela S. C. Takeshita ◽  
Renata S. Mendonça ◽  
Fred B. Bercovitch ◽  
Michael A. Huffman
2021 ◽  
Vol 22 (3) ◽  
pp. 1057
Author(s):  
Magdalena Wójcik-Jagła ◽  
Agata Daszkowska-Golec ◽  
Anna Fiust ◽  
Przemysław Kopeć ◽  
Marcin Rapacz

Mechanisms involved in the de-acclimation of herbaceous plants caused by warm periods during winter are poorly understood. This study identifies the genes associated with this mechanism in winter barley. Seedlings of eight accessions (four tolerant and four susceptible to de-acclimation cultivars and advanced breeding lines) were cold acclimated for three weeks and de-acclimated at 12 °C/5 °C (day/night) for one week. We performed differential expression analysis using RNA sequencing. In addition, reverse-transcription quantitative real-time PCR and enzyme activity analyses were used to investigate changes in the expression of selected genes. The number of transcripts with accumulation level changed in opposite directions during acclimation and de-acclimation was much lower than the number of transcripts with level changed exclusively during one of these processes. The de-acclimation-susceptible accessions showed changes in the expression of a higher number of functionally diverse genes during de-acclimation. Transcripts associated with stress response, especially oxidoreductases, were the most abundant in this group. The results provide novel evidence for the distinct molecular regulation of cold acclimation and de-acclimation. Upregulation of genes controlling developmental changes, typical for spring de-acclimation, was not observed during mid-winter de-acclimation. Mid-winter de-acclimation seems to be perceived as an opportunity to regenerate after stress. Unfortunately, it is competitive to remain in the cold-acclimated state. This study shows that the response to mid-winter de-acclimation is far more expansive in de-acclimation-susceptible cultivars, suggesting that a reduced response to the rising temperature is crucial for de-acclimation tolerance.


2007 ◽  
Vol 44 (3) ◽  
pp. 166-177 ◽  
Author(s):  
M. Winterhalter ◽  
H. A. Adams ◽  
T. Engels ◽  
N. Rahe-Meyer ◽  
J. Zuk ◽  
...  

2013 ◽  
Vol 186 ◽  
pp. 136-144 ◽  
Author(s):  
Carolyn M. Bauer ◽  
Nicholas K. Skaff ◽  
Andrew B. Bernard ◽  
Jessica M. Trevino ◽  
Jacqueline M. Ho ◽  
...  

Author(s):  
David E. Henley ◽  
Joey M. Kaye ◽  
Stafford L. Lightman

In the face of any threat or challenge, either real or perceived, an organism must mount a series of coordinated and specific hormonal, autonomic, immune, and behavioural responses that allow it to either escape or adapt (1–3). To be successful, the characteristics and intensity of the response must match that posed by the threat itself and should last no longer than is necessary. A response that is either inadequate or excessive in terms of its specificity, intensity or duration may result in one or more of a multitude of psychological or physical pathologies (2–5). This concept of threat and the organism’s response to it is frequently recognized and understood as ‘stress’ but is so diverse that it lacks a universally accepted definition (2) and thus is difficult to investigate or study (6). In the early 1900s, Walter Cannon introduced the concept of homoeostasis (4)—an ideal steady state for all physiological processes. Stress has been defined as the state where this ideal is threatened. More easily appreciated, however, are those factors, both intrinsic and extrinsic, which represent a challenge to homoeostasis (termed stressors) and the complex physiological, hormonal, and behavioural responses that occur to restore the balance, the stress response (1). The importance of endocrine systems in this stress response was emphasized by Hans Selye (7), who described the need for multiple, integrated systems to respond in a coordinated fashion following exposure to a particular stressor. Nonspecific activation of the hypothalamic–pituitary–adrenal (HPA) and sympatho-adrenomedullary (SAM) axes occurred following initial exposure to a noxious stimulus. Continued exposure to the same agent has been shown to have lasting and damaging effects on various endocrine, immune, and other systems, although recovery from this state was possible provided the stress was terminated (7). In addition to various noxious agents, numerous potential stressors exist including exertion, physical extremes, trauma, injury, and psychological stress. Indeed, psychological stressors are some of the most potent stimuli of the endocrine stress response particularly when they involve elements of novelty, uncertainty, and unpredictability. This has been highlighted by the observation that anticipating an event can be as potent an activator of the stress response as the event itself (7).


2009 ◽  
Vol 30 (21) ◽  
pp. 2606-2613 ◽  
Author(s):  
Markus Rauchenzauner ◽  
Florian Ernst ◽  
Florian Hintringer ◽  
Hanno Ulmer ◽  
Christoph F. Ebenbichler ◽  
...  

2010 ◽  
Vol 27 ◽  
pp. 223 ◽  
Author(s):  
C. Ozhan ◽  
M. O. Ozhan ◽  
M. A. Suzer ◽  
M. B. Eskin ◽  
I. Kati

2005 ◽  
Vol 22 (Supplement 34) ◽  
pp. 134 ◽  
Author(s):  
M. Georgiou ◽  
Th. Georgiadou ◽  
I. Soumpasis ◽  
R. Ziagka ◽  
E. Sfyra ◽  
...  

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