Release of corticotropin after administration of corticotropin-releasing hormone in depressed patients in relation to the dexamethasone suppression test

1993 ◽  
Vol 87 (2) ◽  
pp. 133-140 ◽  
Author(s):  
B.-E. Thalén ◽  
B.F. Kjellman ◽  
J.-G. Ljunggren ◽  
G. Akner ◽  
B. Kågedal ◽  
...  
1984 ◽  
Vol 144 (3) ◽  
pp. 311-313 ◽  
Author(s):  
D. Ames ◽  
G. Burrows ◽  
B. Davies ◽  
K. Maguire ◽  
T. Norman

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jacob M. Maskal ◽  
Luiz F. Brito ◽  
Alan W. Duttlinger ◽  
Kouassi R. Kpodo ◽  
Betty R. McConn ◽  
...  

AbstractIn utero heat stress alters postnatal physiological and behavioral stress responses in pigs. However, the mechanisms underlying these alterations have not been determined. The study objective was to characterize the postnatal hypothalamic–pituitary–adrenal axis response of in utero heat-stressed pigs. Pigs were subjected to a dexamethasone suppression test followed by a corticotrophin releasing hormone challenge at 10 and 15 weeks of age. Following the challenge, hypothalamic, pituitary, and adrenal tissues were collected from all pigs for mRNA abundance analyses. At 10 weeks of age, in utero heat-stressed pigs had a reduced (P < 0.05) cortisol response to the corticotrophin releasing hormone challenge versus controls. Additionally, the cortisol response tended to be greater overall (P < 0.10) in 15 versus 10-week-old pigs in response to the dexamethasone suppression test. The cortisol response tended to be reduced overall (P < 0.10) in 15 versus 10-week-old pigs in response to the corticotrophin releasing hormone challenge. Hypothalamic corticotropin releasing hormone mRNA abundance tended to be greater (P < 0.10) in in utero heat-stressed versus control pigs at 15-weeks of age. In summary, in utero heat stress altered some aspects of the hypothalamic–pituitary–adrenal axis related to corticotropin releasing hormone signaling, and age influenced this response.


1991 ◽  
Vol 69 (3) ◽  
pp. 878-878
Author(s):  
David Lester

For 10 nations suicide rates were not correlated with the percentages of depressed patients who responded abnormally to the Dexamethasone Suppression Test.


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