INTERLEUKIN-6 STIMULATES THE HYPOTHALAMUS-PITUITARY-ADRENOCORTICAL AXIS IN MAN

被引:122
作者
SPATHSCHWALBE, E
BORN, J
SCHREZENMEIER, H
BORSTEIN, SR
STROMEYER, P
DRECHSLER, S
FEHM, HL
PORZSOLT, F
机构
[1] UNIV LUBECK, DEPT CLIN NEUROENDOCRINOL, D-23538 LUBECK, GERMANY
[2] UNIV LUBECK, DEPT INTERNAL MED, D-23538 LUBECK, GERMANY
[3] SANDOZ PHARMA LTD, D-53113 BONN, GERMANY
关键词
D O I
10.1210/jc.79.4.1212
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A recent study in humans, animal studies, and in vitro data have suggested that interleukin-6 (IL-6) stimulates the secretory activity of the hypothalamus-pituitary-adrenocortical (HPA) axis. In a phase II study, one female and six male patients with metastatic renal cell carcinoma received IL-6 to evaluate a possible antitumor effect of IL-6. This offered the possibility of investigating the influence of IL-6 on the HPA axis in man. The subjects were studied 1 day before, on day 1, and on day 21 of IL-6 therapy (150 mu g administered sc every day at 0900 h). Blood samples were taken at 0900, 1100, 1300, 1600, and 2000 h the day before, on day 1 of IL-6 therapy, 24 h after the first IL-6 injection, and on day 21 of IL-6 treatment. Plasma ACTH and cortisol levels promptly followed the rise of IL-6, which peaked 4 h after administration. They were significantly (P < 0.05) higher at 1100 and 1300 h on day 1 of IL-6 therapy compared with the corresponding plasma levels the day before IL-6 treatment. Cortisol concentrations remained significantly increased at 1600 and 2000 h after IL-6 administration. Twenty-four hours after the first IL-6 administration, IL-6, ACTH, and cortisol levels had reached preinjection values. Although plasma cortisol levels were similar on days 1 and 21, ACTH levels were lower on day 21 (than on day 1), but significantly elevated at 1100 h compared with levels on the day before the first IL-6 injection. Results confirming the very recent data of another study demonstrate a stimulating effect of IL-6 on the HPA axis in man. They support the notion that IL-6 is one of the cytokines involved in the interaction between the immune system and the HPA axis.
引用
收藏
页码:1212 / 1214
页数:3
相关论文
共 14 条
[1]   INTERLEUKIN-6 IN CLINICAL MEDICINE [J].
BAUER, J ;
HERRMANN, F .
ANNALS OF HEMATOLOGY, 1991, 62 (06) :203-210
[2]   THE EFFECTS OF RECOMBINANT HUMAN INTERLEUKIN (IL)-1-ALPHA, IL-1-BETA OR IL-6 ON HYPOTHALAMO-PITUITARY-ADRENAL AXIS ACTIVATION [J].
HARBUZ, MS ;
STEPHANOU, A ;
SARLIS, N ;
LIGHTMAN, SL .
JOURNAL OF ENDOCRINOLOGY, 1992, 133 (03) :349-355
[3]   CYTOKINES AND ENDOCRINE FUNCTION - AN INTERACTION BETWEEN THE IMMUNE AND NEUROENDOCRINE SYSTEMS [J].
IMURA, H ;
FUKATA, J ;
MORI, T .
CLINICAL ENDOCRINOLOGY, 1991, 35 (02) :107-115
[4]   THE EFFECT OF INTERLEUKIN-6 ON PITUITARY-HORMONE RELEASE INVIVO AND INVITRO [J].
LYSON, K ;
MCCANN, SM .
NEUROENDOCRINOLOGY, 1991, 54 (03) :262-266
[5]   RECOMBINANT INTERLEUKIN-6 ACTIVATES THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS IN HUMANS [J].
MASTORAKOS, G ;
CHROUSOS, GP ;
WEBER, JS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (06) :1690-1694
[6]   A CENTRAL MECHANISM IS INVOLVED IN THE SECRETION OF ACTH IN RESPONSE TO IL-6 IN RATS - COMPARISON TO AND INTERACTION WITH IL-1-BETA [J].
MATTA, SG ;
WEATHERBEE, J ;
SHARP, BM .
NEUROENDOCRINOLOGY, 1992, 56 (04) :516-525
[7]   INTERLEUKIN-6 STIMULATES THE SECRETION OF ADRENOCORTICOTROPIC HORMONE IN CONSCIOUS, FREELY-MOVING RATS [J].
NAITOH, Y ;
FUKATA, J ;
TOMINAGA, T ;
NAKAI, Y ;
TAMAI, S ;
MORI, K ;
IMURA, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 155 (03) :1459-1463
[8]   INTERLEUKINS-1 AND INTERLEUKINS-6 STIMULATE THE RELEASE OF CORTICOTROPIN-RELEASING HORMONE-41 FROM RAT HYPOTHALAMUS INVITRO VIA THE EICOSANOID CYCLOOXYGENASE PATHWAY [J].
NAVARRA, P ;
TSAGARAKIS, S ;
FARIA, MS ;
REES, LH ;
BESSER, GM ;
GROSSMAN, AB .
ENDOCRINOLOGY, 1991, 128 (01) :37-44
[9]   BINDING-SITES FOR INTERLEUKIN-6 IN THE ANTERIOR-PITUITARY GLAND [J].
OHMICHI, M ;
HIROTA, K ;
KOIKE, K ;
KURACHI, H ;
OHTSUKA, S ;
MATSUZAKI, N ;
YAMAGUCHI, M ;
MIYAKE, A ;
TANIZAWA, O .
NEUROENDOCRINOLOGY, 1992, 55 (02) :199-203
[10]  
SALAS MA, 1990, CLIN EXP IMMUNOL, V79, P470