scholarly journals Relationships between rapid changes in local aromatase activity and estradiol concentrations in male and female quail brain

2014 ◽  
Vol 65 (2) ◽  
pp. 154-164 ◽  
Author(s):  
M.J. Dickens ◽  
C. de Bournonville ◽  
J. Balthazart ◽  
C.A. Cornil
2017 ◽  
Vol 29 (11) ◽  
pp. e12542 ◽  
Author(s):  
C. de Bournonville ◽  
G. F. Ball ◽  
J. Balthazart ◽  
C. A. Cornil

Endocrinology ◽  
2011 ◽  
Vol 152 (11) ◽  
pp. 4242-4251 ◽  
Author(s):  
Molly J. Dickens ◽  
Charlotte A. Cornil ◽  
Jacques Balthazart

The rapid and temporary suppression of reproductive behavior is often assumed to be an important feature of the adaptive acute stress response. However, how this suppression operates at the mechanistic level is poorly understood. The enzyme aromatase converts testosterone to estradiol in the brain to activate reproductive behavior in male Japanese quail (Coturnix japonica). The discovery of rapid and reversible modification of aromatase activity (AA) provides a potential mechanism for fast, stress-induced changes in behavior. We investigated the effects of acute stress on AA in both sexes by measuring enzyme activity in all aromatase-expressing brain nuclei before, during, and after 30 min of acute restraint stress. We show here that acute stress rapidly alters AA in the male and female brain and that these changes are specific to the brain nuclei and sex of the individual. Specifically, acute stress rapidly (5 min) increased AA in the male medial preoptic nucleus, a region controlling male reproductive behavior; in females, a similar increase was also observed, but it appeared delayed (15 min) and had smaller amplitude. In the ventromedial and tuberal hypothalamus, regions associated with female reproductive behavior, stress induced a quick and sustained decrease in AA in females, but in males, only a slight increase (ventromedial) or no change (tuberal) in AA was observed. Effects of acute stress on brain estrogen production, therefore, represent one potential way through which stress affects reproduction.


Neuroscience ◽  
2004 ◽  
Vol 123 (3) ◽  
pp. 647-666 ◽  
Author(s):  
C.R Dermon ◽  
A Stamatakis ◽  
S Giakoumaki ◽  
J Balthazart

1996 ◽  
Vol 148 (2) ◽  
pp. 233-239 ◽  
Author(s):  
A Gobbetti ◽  
M Zerani

Abstract To clarify the endocrine mechanism involved in the short captivity stress in the water frog, Rana esculenta, the activity of 9-ketoreductase, the enzyme which converts prostaglandin E2 (PGE2) into prostaglandin F2α (PGF2α), and aromatase, which converts testosterone into oestradiol-17β, were studied. Adult male and female frogs were sacrificed 0, 1·5, 3, 6, 12, 24, 48, 72, 168 and 336 h after capture in the field. PGE2, PGF2α, progesterone, testosterone, oestradiol-17β and corticosterone plasma levels were detected by RIA at each time point. 9-Ketoreductase (conversion of [3H]PGE2 into [3H]PGF2α) and aromatase (conversion of [3H]testosterone into [3H]oestradiol-17β) activities in the brain, testis, ovary and interrenal were also determined at each time point. After capture, levels of plasma PGF2α increased (male: 228%; female: 288%) and PGE2 decreased (male: 68%; female: 81%) at 1·5 h, oestradiol-17β increased (male: 399%; female: 425%) and testosterone decreased (male: 87%; female: 83%) at 6 h, and corticosterone increased (male: 421%; female: 426%) at 72 h. 9-Ketoreductase activity in the brain was enhanced at 1·5 h after capture (male: 249%; female: 262%); aromatase activity increased at 6 h in the testis (261%), ovary (273%) and interrenal (male: 227%; female: 267%). These results indicate that short captivity stress could induce an increase in plasma PGF2α through activation of brain 9-ketoreductase. In turn, PGF2α might enhance the levels of circulating oestradiol-17β through activation of gonadal and interrenal aromatase. Journal of Endocrinology (1996) 148, 233–239


2011 ◽  
Vol 170 (1) ◽  
pp. 180-188 ◽  
Author(s):  
Cornelia Voigt ◽  
Gregory F. Ball ◽  
Jacques Balthazart

1997 ◽  
Vol 37 (5) ◽  
pp. 505-514 ◽  
Author(s):  
JEE-YAU LEE ◽  
LESLIE A HOLDEN ◽  
MUSTAFA B.A DJAMGOZ

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