The present work describes time-dependent changes in the content of corticotropin-releasing hormone (CRH), adrenocorticotropin (ACTH), and P-endorphin (P-EP) in the hypothalamus (HT) and anterior pituitary (AP) and in the concentration of ACTH and P-EP in the plasma during the 17P estradiol (E,) ben
Lack of effect of interleukins 1α and 1β, during in vitro perifusion, on anterior pituitary release of adrenocorticotropic hormone and β endorphin in the male rat
✍ Scribed by S. Mélik Parsadaniantz; V. Lenoir; B. Terlain; B. Kerdelhué
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 803 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
It has been demonstrated that interleukin 1 (ILl) injection provokes a great variety of biological effects, notably an activation of the corticotropic axis, increasing plasma adrenocorticotropic hormone (ACTH) and corticosterone. However, the primary site of action of IL1 is still controversial. In the present study, we first verified the in vivo capability of human interleukins la (hILla) and l p (hIL1p) to release ACTH and p endorphin (p EP) in the normal male rat, before investigating, through an anterior pituitary (AP) perifusion system, the h I L l a and hILl p effects on basal and corticotropin-releasing factor (CRF)-induced ACTH and p EP secretions.
This system enabled the examination of a dynamic profile of hormones secretion, avoiding the possibility of feedback mechanisms, as is the case with the use of regular but very often longtime incubations.
The results showed that in a perifusion system, with a short duration treatment (below 2 hr) compatible with the kinetics of action observed in vivo, basal and CRF-induced ACTH and p E P release were not modified in the presence of a broad range of concentrations (from lo-'* to lo-' M) of h I L l a or hILIp. Taken together, these results clearly show that in an in vitro situation close to physiological conditions, the primary site of action of h I L l a and hILlP on ACTH and 0 EP release is not located at the AP level in the male rat.
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