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
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.