Regulation of the HPA axis by cytokines

被引:222
作者
Turnbull, AV
Rivier, C
机构
[1] Clayton Foundation Laboratories, Peptide Biology, The Salk Institute, La Jolla, CA 92037
关键词
D O I
10.1006/brbi.1995.1026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytokines are a group of polypeptide mediators, classically associated with the regulation of immunity and inflammation. However, these peptides regulate not only local immune/inflammatory responses, but also elicit many CNS-mediated responses which accompany such immune/inflammalory reactions. This article reviews the evidence that interleukin (IL)-1, IL-6, and tumor necrosis factor alpha (TNF alpha) produce hypothalamo-pituitary-adrenal (HPA) axis activation in response to various threats to homeostasis. To aid such an examination, and to gain insights into the potential mechanisms by which these cytokines influence the HPA axis, experimental findings are discussed within a framework of criteria. If a particular cytokine plays a significant role in the regulation of the HPA axis in response to a particular pathophysiology, then necessarily: (1) receptors for that cytokine should be present within tissues associated with the HPA axis; (2) administration of that cytokine should elicit HPA activation; (3) the HPA axis should be exposed to that cytokine; and (4) inhibition of the action of that cytokine should prevent HPA activation. The evidence discussed indicates that some, if not all, of these criteria are met for each of IL-1, IL-6, and TNF alpha. However, the extensive interactions between different cytokines, the broad spectrum of pathophysiologies associated with increased cytokine production (including inflammatory and non-inflammatory stresses), and the number of tissues/cells capable of either synthesizing or responding to cytokines, suggest that multiple mechanisms mediate the influence of cytokines on the HPA axis. (C) 1995 Academic Press, Inc.
引用
收藏
页码:253 / 275
页数:23
相关论文
共 189 条
[1]  
ADERKA D, 1989, J IMMUNOL, V143, P3517
[2]   LIPOPOLYSACCHARIDE INDUCES HUMAN INTERLEUKIN-1 RECEPTOR ANTAGONIST AND INTERLEUKIN-1 PRODUCTION IN THE SAME CELL [J].
ANDERSSON, J ;
BJORK, L ;
DINARELLO, CA ;
TOWBIN, H ;
ANDERSSON, U .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (10) :2617-2623
[3]   INTERLEUKIN-1-BETA ENHANCES CORTICOSTERONE SECRETION BY ACTING DIRECTLY ON THE RAT ADRENAL-GLAND [J].
ANDREIS, PG ;
NERI, G ;
BELLONI, AS ;
MAZZOCCHI, G ;
KASPRZAK, A ;
NUSSDORFER, GG .
ENDOCRINOLOGY, 1991, 129 (01) :53-57
[4]   DIFFERENTIAL ALTERATIONS IN PLASMA IL-L AND TNF LEVELS AFTER TRAUMA AND HEMORRHAGE [J].
AYALA, A ;
WANG, P ;
BA, ZF ;
PERRIN, MM ;
ERTEL, W ;
CHAUDRY, IH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (01) :R167-R171
[5]   SYSTEMIC CYTOKINE RESPONSE AFTER MAJOR SURGERY [J].
BAIGRIE, RJ ;
LAMONT, PM ;
KWIATKOWSKI, D ;
DALLMAN, MJ ;
MORRIS, PJ .
BRITISH JOURNAL OF SURGERY, 1992, 79 (08) :757-760
[6]   THE CYTOKINE NETWORK [J].
BALKWILL, FR ;
BURKE, F .
IMMUNOLOGY TODAY, 1989, 10 (09) :299-303
[7]   BRAIN INTERLEUKIN-1 GENE-EXPRESSION INDUCED BY PERIPHERAL LIPOPOLYSACCHARIDE ADMINISTRATION [J].
BAN, E ;
HAOUR, F ;
LENSTRA, R .
CYTOKINE, 1992, 4 (01) :48-54
[8]   RECEPTORS FOR INTERLEUKIN-1 (ALPHA AND BETA) IN MOUSE-BRAIN - MAPPING AND NEURONAL LOCALIZATION IN HIPPOCAMPUS [J].
BAN, E ;
MILON, G ;
PRUDHOMME, N ;
FILLION, G ;
HAOUR, F .
NEUROSCIENCE, 1991, 43 (01) :21-30
[9]   PENETRATION OF INTERLEUKIN-6 ACROSS THE MURINE BLOOD-BRAIN-BARRIER [J].
BANKS, WA ;
KASTIN, AJ ;
GUTIERREZ, EG .
NEUROSCIENCE LETTERS, 1994, 179 (1-2) :53-56
[10]  
BANKS WA, 1991, J PHARMACOL EXP THER, V259, P988