EFFECT OF INTERLEUKIN-1-BETA ON PLASMA ACTH, BETA-ENDORPHIN, AND CORTICOSTERONE LEVELS IN INFANT AND PREPUBERTAL RATS

Citation
I. Barna et al., EFFECT OF INTERLEUKIN-1-BETA ON PLASMA ACTH, BETA-ENDORPHIN, AND CORTICOSTERONE LEVELS IN INFANT AND PREPUBERTAL RATS, Pediatric research, 37(6), 1995, pp. 714-719
Citations number
30
Categorie Soggetti
Pediatrics
Journal title
ISSN journal
00313998
Volume
37
Issue
6
Year of publication
1995
Pages
714 - 719
Database
ISI
SICI code
0031-3998(1995)37:6<714:EOIOPA>2.0.ZU;2-K
Abstract
IL-1 beta is known to enhance ACTH release from the anterior pituitary in the adult rat, mainly by simulating the hypothalamic ACTH-releasin g hormone (CRH) release, but it seems to have a direct effect on the p ituitary and on the adrenal hormone secretion, too. The effect of IL-1 beta on the beta-endorphin (beta E) secretion from the intermediate l obe is less well studied. There is very little information on the effe ct of IL-1 beta on the hypothalamic-pituitary-adrenal axis (HPAA) in t he postnatal rat, which is a special period, because the reactivity of the HPAA is blunted. The effect of IL-1 beta in this period seemed to be of special interest, because neither the immune nor the endocrine system is fully developed. In the present study we tested the 30- and 120-min effect of intraperitoneally administered 0.5 and 100 ng/g body weight IL-1 beta on the plasma immunoreactive (ir) ACTH, beta E, and corticosterone (CS) levels in the 10-d-old (infant) and 30-d-old (prep ubertal) rat. Generally, the ir-ACTH, ir-beta E, and ir-CS levels were significantly higher in prepubertal than in infant rats. Hormone leve ls were more enhanced by the higher dose of IL-1 beta, and changes wer e more pronounced at 120 min than at 30 min. The relative increase of ir-ACTH and ir-beta E was smaller in the infant than in the prepuberta l rat. In contrast, the relative increase of ir-CS was more pronounced in the infant rat. Changes in plasma ir-beta E and ir-ACTH levels wer e not parallel, suggesting different responsiveness of the anterior pi tuitary corticotrophs and intermediate pituitary melanotrophs to IL-1 beta stimulation. The age-related peculiarities in response to IL-1 be ta could be due to a different secretory capacity andior different kin etics of the HPAA in the infant (10-d-old) and prepubertal (30-d-old) rat. There could be a change in sensitivity of different components of the HPAA (hypothalamus, pituitary, adrenal) to IL-1 beta during the p ostnatal development.