THE REPRODUCTIVE ENDOCRINE SYSTEM IN CYSTIC FIBROSIS: 2. CHANGES IN GONADOTROPHINS AND SEX STEROIDS FOLLOWING LHRH

1982 ◽  
Vol 16 (2) ◽  
pp. 127-137 ◽  
Author(s):  
E. O. REITER ◽  
R. C. STERN ◽  
A. W. ROOT
2002 ◽  
Vol 282 (1) ◽  
pp. E215-E221 ◽  
Author(s):  
Lionel Verdier ◽  
Yves Boirie ◽  
Sebastien Van Drieesche ◽  
Michelle Mignon ◽  
Rene-Jean Begue ◽  
...  

Glutamine synthetase, a key enzyme in the production of glutamine, is known to be induced by glucocorticoids and preserved in skeletal muscle during aging, but the effect of other steroids, such as sex steroids (progesterone, estradiol), is unknown in vivo. The aim of this study was to determine whether progesterone or estradiol plays a role in the regulation of glutamine synthetase (GS) with aging. The effects of glucocorticoids and sex steroids on muscle GS activity and mRNA expression were measured in adult (6–8 mo; n = 7 in each group) and aged (26 mo; n= 10 in each group) female Wistar rats after adrenalectomy (ADX), ovariectomy (OV), or both (ADXOV) and were compared with those in sham-operated (Sham) control rats. In tibialis anterior muscle, ADX noticeably decreased both GS activity and expression irrespective of age (50–60%; P < 0.05), whereas OV had no effect at either age. Progesterone and estradiol replacement had no effect on the recovery of muscle GS response in either ADX or OV rats, regardless of age. In contrast, heart GS activity was decreased by ADX in aged animals only. These results suggest that the reproductive endocrine status of female rats does not affect muscle GS activity either in muscle or in heart, in young or aged animals, and that the heart GS response to steroids may be differently regulated in aged rats.


1983 ◽  
Vol 245 (4) ◽  
pp. R473-R477 ◽  
Author(s):  
W. R. Smith

Some qualitative dynamical models of endocrine systems are considered and analyzed, with the reproductive endocrine system as an example. The models considered are systems of nonlinear ordinary differential equations describing the rates of change of the hormonal concentrations with time. This type of general approach, which requires only the incorporation of the basic qualitative features of the interactions present in the underlying system into the model, is a potentially powerful tool for elucidating possible mechanisms for observed qualitative patterns of hormonal dynamics.


2010 ◽  
Vol 50 (1) ◽  
pp. 53-62 ◽  
Author(s):  
K. Kubokawa ◽  
Y. Tando ◽  
S. Roy

2016 ◽  
Vol 175 ◽  
pp. 205-212 ◽  
Author(s):  
Yujing Su ◽  
Li Li ◽  
Jie Hou ◽  
Ning Wu ◽  
Wang Lin ◽  
...  

mBio ◽  
2020 ◽  
Vol 11 (5) ◽  
Author(s):  
Celine Vidaillac ◽  
Valerie Fei Lee Yong ◽  
Marie-Stephanie Aschtgen ◽  
Jing Qu ◽  
Shuowei Yang ◽  
...  

ABSTRACT Estrogen, a major female sex steroid hormone, has been shown to promote the selection of mucoid Pseudomonas aeruginosa in the airways of patients with chronic respiratory diseases, including cystic fibrosis. This results in long-term persistence, poorer clinical outcomes, and limited therapeutic options. In this study, we demonstrate that at physiological concentrations, sex steroids, including testosterone and estriol, induce membrane stress responses in P. aeruginosa. This is characterized by increased virulence and consequent inflammation and release of proinflammatory outer membrane vesicles promoting in vivo persistence of the bacteria. The steroid-induced P. aeruginosa response correlates with the molecular polarity of the hormones and membrane fluidic properties of the bacteria. This novel mechanism of interaction between sex steroids and P. aeruginosa explicates the reported increased disease severity observed in females with cystic fibrosis and provides evidence for the therapeutic potential of the modulation of sex steroids to achieve better clinical outcomes in patients with hormone-responsive strains. IMPORTANCE Molecular mechanisms by which sex steroids interact with P. aeruginosa to modulate its virulence have yet to be reported. Our work provides the first characterization of a steroid-induced membrane stress mechanism promoting P. aeruginosa virulence, which includes the release of proinflammatory outer membrane vesicles, resulting in inflammation, host tissue damage, and reduced bacterial clearance. We further demonstrate that at nanomolar (physiological) concentrations, male and female sex steroids promote virulence in clinical strains of P. aeruginosa based on their dynamic membrane fluidic properties. This work provides, for the first-time, mechanistic insight to better understand and predict the P. aeruginosa related response to sex steroids and explain the interindividual patient variability observed in respiratory diseases such as cystic fibrosis that are complicated by gender differences and chronic P. aeruginosa infection.


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