IGF-I/IGFBPs system response to endotoxin challenge in sheep

被引:33
作者
Briard, N
Dadoun, F
Pommier, G
Sauze, N
Lebouc, Y
Oliver, C
Dutour, A
机构
[1] Hop Nord Marseille, Serv Endocrinol Malad Metab & Nutr, F-13915 Marseille 20, France
[2] Inst Federat Jean Roche, INSERM, U501, Lab Neuroendocrinol Expt, F-13916 Marseille 20, France
[3] CNRS, ESA 6032, Unite Interact Prot & Differenciat Cellule Tumora, F-13385 Marseille, France
[4] Hop Trousseau, F-75571 Paris 12, France
关键词
D O I
10.1677/joe.0.1640361
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endotoxin (LPS), a membrane component of gram-negative bacteria produces multiple endocrine and metabolic effects that mimic those seen in acute sepsis. It induces species-dependent alterations of the growth hormone (GH) axis that may participate in the shift of the metabolism towards catabolic events. Humans and sheep show increased GH secretion in response to LPS, as opposed to rats, which have been the most studied. The purpose of our work was to evaluate the effects in intact rams of an acute intravenous administration of a high dose of LPS on the insulin-like growth factor (IGF)-I/IGF-binding proteins (IGFBPs) system and to analyse the temporal relationship of GH axis changes with those of several hormonal and metabolic parameters such as somatostatin, cortisol, insulin, and glucose. LPS induced a late moderate decrease of total IGF-I plasma levels following a 5-h steady-state period (-26.6 +/- 4.2%, P<0.05, 9 h after LPS), despite a biphasic and sustained increase of GH secretion in the same animals (2.48 +/- 0.39 ng/ml 2 h after LPS and 2.7 +/- 0.37 ng/ml 5 h after LPS vs 0.77 +/- 0.10 before LPS; Briard et al. 1998a). Western ligand blot analysis in IGFBPs showed an early short-lasting increase in IGFBP-1 (188.8 +/- 39% P<0.05, 3 h after LPS). No significant change was seen for either IGFBP-2, -3 or -4. We observed a marked and sustained increase in cortisol (128.18 +/- 7.21 ng/ml 3 h after LPS, vs 21.17 +/- 4.22 before LPS). Insulin also increased (27.69 +/- 3.90 mu U/ml 3 h after LPS, vs 13.48 +/- 1.69 before LPS) and its burst coincided with that of IGFBP-1. Moderately decreased IGF-I and increased IGFBP-1 plasma levels contrasted with the sustained increase in GH secretion that we recently described, thereby suggesting that endotoxin causes a state of resistance to GH. This may be exacerbated by reduced IGF-I bioavailability and/or action, and which may participate in the pathophysiology of the catabolic state seen in sepsis. The temporal analysis of hormone responses suggests that endotoxin-induced alterations of the IGF-I/IGFBPs system may involve the prolonged and substantial somatostatin rise that we recently demonstrated, together with an increase in glucocorticoid and cytokine as more generally assumed.
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页码:361 / 369
页数:9
相关论文
共 63 条
[51]   REGULATION OF INSULIN-LIKE GROWTH FACTOR-I (IGF-I) AND IGF-BINDING PROTEIN-1 GENE-TRANSCRIPTION BY HORMONES AND PROVISION OF AMINO-ACIDS IN RAT HEPATOCYTES [J].
PAO, CI ;
FARMER, PK ;
BEGOVIC, S ;
VILLAFUERTE, BC ;
WU, GJ ;
ROBERTSON, DG ;
PHILLIPS, LS .
MOLECULAR ENDOCRINOLOGY, 1993, 7 (12) :1561-1568
[52]  
PETER AT, 1989, AM J VET RES, V50, P368
[53]   SOMATOSTATIN ANALOG INDUCES INSULIN-LIKE GROWTH-FACTOR BINDING PROTEIN-1 (IGFBP-1) EXPRESSION IN HUMAN HEPATOMA-CELLS [J].
REN, SG ;
EZZAT, S ;
MELMED, S ;
BRAUNSTEIN, GD .
ENDOCRINOLOGY, 1992, 131 (05) :2479-2481
[54]   IN THE MOUSE, THE ACTIVATION OF THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS BY A LIPOPOLYSACCHARIDE (ENDOTOXIN) IS MEDIATED THROUGH INTERLEUKIN-1 [J].
RIVIER, C ;
CHIZZONITE, R ;
VALE, W .
ENDOCRINOLOGY, 1989, 125 (06) :2800-2805
[55]   IL-6 stimulation of insulin-like growth factor binding protein (IGFBP)-1 production [J].
Samstein, B ;
Hoimes, ML ;
Fan, J ;
Frost, RA ;
Gelato, MC ;
Lang, CH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 228 (02) :611-615
[56]   Effects of endotoxin lipopolysaccharide administration on the somatotropic axis [J].
Soto, L ;
Martín, AI ;
Millán, S ;
Vara, E ;
López-Calderón, A .
JOURNAL OF ENDOCRINOLOGY, 1998, 159 (02) :239-246
[57]   ON THE NEUROENDOCRINE ROLE OF INSULIN-LIKE GROWTH-FACTOR-1 AND FACTOR-II IN THE REGULATION OF GROWTH-HORMONE SECRETION [J].
SPENCER, GSG ;
BERRY, C ;
HODGKINSON, SC ;
BASS, JJ .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1993, 4 (06) :538-542
[58]   NUTRITIONAL REGULATION OF THE INSULIN-LIKE GROWTH-FACTORS [J].
THISSEN, JP ;
KETELSLEGERS, JM ;
UNDERWOOD, LE .
ENDOCRINE REVIEWS, 1994, 15 (01) :80-101
[59]   Inhibition by interleukin-1 beta and tumor necrosis factor-alpha of the insulin-like growth factor I messenger ribonucleic acid response to growth hormone in rat hepatocyte primary culture [J].
Thissen, JP ;
Verniers, J .
ENDOCRINOLOGY, 1997, 138 (03) :1078-1084
[60]   ACTIVATION OF THE HYPOTHALAMUS-PITUITARY-ADRENAL AXIS BY BACTERIAL-ENDOTOXINS - ROUTES AND INTERMEDIATE [J].
TILDERS, FJH ;
DERIJK, RH ;
VANDAM, AM ;
VINCENT, VAM ;
SCHOTANUS, K ;
PERSOONS, JHA .
PSYCHONEUROENDOCRINOLOGY, 1994, 19 (02) :209-232