Mouse interleukin-6 stimulates the HPA axis and increases brain tryptophan and serotonin metabolism

被引:81
作者
Wang, JP [1 ]
Dunn, AJ [1 ]
机构
[1] Louisiana State Univ, Med Ctr, Dept Pharmacol & Therapeut, Shreveport, LA 71103 USA
关键词
interleukin-6; ACTH; corticosterone; tryptophan; serotonin;
D O I
10.1016/S0197-0186(98)00016-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuroendocrine and neurochemical responses were studied following administration of recombinant mouse IL-6 (mIL-6) to mice. Intravenous (iv) or intraperitoneal (ip) injection of mIL-6 caused a rapid and short-lived activation of the hypothalamo-pituitary-adrenocortical (HPA) axis, as indicated by increases in plasma ACTH and corticosterone, with peak responses around 30-60 min. These responses contrast with those to ip mIL-1 beta which is substantially more potent and induces a greater response which does not peak until about 2 h following ip administration. Unlike IL-1 and lipopolysaccharide (LPS), IL-6 had no detectable effect on norepinephrine metabolism. However, tryptophan concentrations were elevated in most brain regions studied 1-2 h following iv mIL-6, and 2 h following ip mIL-6, significantly later than the peak HPA response. 5-hydroxyindoleacetic acid (5-HIAA) and the ratio of 5-HIAA to serotonin (5-HT) were elevated at around the same time in the brain stem, and occasionally in other brain regions. These responses were observed at doses of mIL-6 as low as 0.25 mu g, and near maximal effects were achieved by 0.5 mu g. Recombinant human IL-6 elicited similar responses, but was significantly less potent. Heal-treated mIL-6 elicited none of the responses. Serum amyloid A protein (SAA) concentrations were not elevated until 4 h after iv or ip mIL-6 administration, suggesting that the neuroendocrine and neurochemical changes were not secondary to an acute phase protein response. Intracerebroventricular injection of mIL-6 also elevated tryptophan and 5-HIAA in the hypothalamus and brain stem. Pretreatment of mice with the cydooxygenase inhibitor, indomethacin, or the nitric oxide synthase inhibitor, N-omega-nitro-L-arginine methyl ester (L-NAME) did not attenuate the mIL-6 induced neuroendocrine or neurochemical responses. However, the ganglionic blocking drug, chlorisondamine, prevented the increases in tryptophan and S-HIAA:5-HT ratios. IL-6 may contribute to the HPA and indoleaminergic responses to LPS and IL-1. It is possible that the increases of tryptophan and serotonin metabolism may contribute to some of the biological effects of IL-6. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:143 / 154
页数:12
相关论文
共 67 条
[21]   BRAIN SEROTONIN CONTENT - PHYSIOLOGICAL DEPENDENCE ON PLASMA TRYPTOPHAN LEVELS [J].
FERNSTROM, JD ;
WURTMAN, RJ .
SCIENCE, 1971, 173 (3992) :149-+
[22]   PERMISSIVE ROLE OF GLUCOCORTICOIDS ON INTERLEUKIN-1 ACTIVATION OF THE HYPOTHALAMIC SEROTONERGIC SYSTEM [J].
GEMMA, C ;
DELUIGI, A ;
DESIMONI, MG .
BRAIN RESEARCH, 1994, 651 (1-2) :169-173
[23]   DOPAMINE INVOLVEMENT IN ACTH-INDUCED GROOMING BEHAVIOR [J].
GUILD, AL ;
DUNN, AJ .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1982, 17 (01) :31-36
[24]  
Hartmann E., 1984, PROGR TRYPTOPHAN SER, P297
[25]   INTERLEUKIN-1, INTERLEUKIN-6 - MESSENGERS IN THE NEUROENDOCRINE IMMUNE-SYSTEM [J].
HOOGHEPETERS, E ;
VELKENIERS, B ;
VANHAELST, L ;
HOOGHE, R .
PATHOLOGY RESEARCH AND PRACTICE, 1991, 187 (05) :622-625
[26]   EFFECTS OF L-TRYPTOPHAN ON SHORT-TERM FOOD-INTAKE IN LEAN MEN [J].
HRBOTICKY, N ;
LEITER, LA ;
ANDERSON, GH .
NUTRITION RESEARCH, 1985, 5 (06) :595-607
[27]   INTERLEUKIN-6 AN ENDOCRINE CYTOKINE [J].
JONES, TH .
CLINICAL ENDOCRINOLOGY, 1994, 40 (06) :703-713
[28]   ADRENOCORTICOTROPIN RELEASE INDUCED BY INTRACEREBROVENTRICULAR INJECTION OF RECOMBINANT HUMAN INTERLEUKIN-1 IN RATS - POSSIBLE INVOLVEMENT OF PROSTAGLANDIN [J].
KATSUURA, G ;
GOTTSCHALL, PE ;
DAHL, RR ;
ARIMURA, A .
ENDOCRINOLOGY, 1988, 122 (05) :1773-1779
[29]   ENDOTOXIN ADMINISTRATION STIMULATES CEREBRAL CATECHOLAMINE RELEASE IN FREELY MOVING RATS AS ASSESSED BY MICRODIALYSIS [J].
LAVICKY, J ;
DUNN, AJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 1995, 40 (03) :407-413
[30]   INDUCTION OF INTERLEUKIN-6 BY HUMAN AND MURINE RECOMBINANT INTERLEUKIN-1 IN MICE [J].
LIBERT, C ;
BROUCKAERT, P ;
SHAW, A ;
FIERS, W .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (03) :691-694