Simultaneous changes in central and peripheral components of the hypothalamus-pituitary-thyroid axis in lipopolysaccharide-induced acute illness in mice

被引:124
作者
Boelen, A [1 ]
Kwakkel, J [1 ]
Thijssen-Timmer, DC [1 ]
Alkemade, A [1 ]
Fliers, E [1 ]
Wiersinga, WM [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Endocrinol & Metab, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1677/joe.0.1820315
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
During illness, major changes in thyroid hormone metabolism and regulation occur; these are collectively known as non-thyroidal illness and are characterized by decreased serum triiodothyronine (T-3) and thyroxine (T-4) without an increase in serum TSH. Whether alterations in the central part of the hypothalamus-pituitary-thyroid (HPT) axis precede changes in peripheral thyroid hormone metabolism instead of vice versa, or occur simultaneously, is presently unknown. We therefore studied the time-course of changes in thyroid hormone metabolism in the HPT axis of mice during acute illness induced by bacterial endotoxin (lipopolysaccharide; LPS). LPS rapidly induced interleukin-1beta mRNA expression in the hypothalamus, pituitary, thyroid and liver. This was followed by almost simultaneous changes in the pituitary (decreased expression of thyroid receptor (TR)-beta2, TSHbeta and 5'-deiodinase (D1) mRNAs), the thyroid (decreased TSH receptor mRNA) and the liver (decreased TRbeta1 and D1 mRNA). In the hypothalamus, type 2 deiodinase mRNA expression was strongly increased whereas preproTRH mRNA expression did not change after LPS. Serum T-3 and T-4 fell only after 24 h. Our results suggested almost simultaneous involvement of the whole HPT axis in the downregulation of thyroid hormone metabolism during acute illness.
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页码:315 / 323
页数:9
相关论文
共 25 条
[1]  
[Anonymous], 1987, MULTIPLE COMP PROCED, DOI DOI 10.1002/9780470316672
[2]   REDUCED TISSUE THYROID-HORMONE LEVELS IN FATAL ILLNESS [J].
AREM, R ;
WIENER, GJ ;
KAPLAN, SG ;
KIM, HS ;
REICHLIN, S ;
KAPLAN, MM .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1993, 42 (09) :1102-1108
[3]   Contribution of interleukin-12 to the pathogenesis of non-thyroidal illness [J].
Boelen, A ;
Kwakkel, J ;
Schiphort, MPT ;
Baur, A ;
Köhrle, J ;
Wiersinga, WM .
HORMONE AND METABOLIC RESEARCH, 2004, 36 (02) :101-106
[4]   Induced illness in interleukin-6 (IL-6) knock-out mice: A causal role of IL-6 in the development of the low 3,5,3'-triiodothyronine syndrome [J].
Boelen, A ;
Maas, MAW ;
Lowik, CWGM ;
Platvoet, MC ;
Wiersinga, WM .
ENDOCRINOLOGY, 1996, 137 (12) :5250-5254
[5]   THE ROLE OF CYTOKINES IN THE LIPOPOLYSACCHARIDE-INDUCED SICK EUTHYROID SYNDROME IN MICE [J].
BOELEN, A ;
PLATVOETTERSCHIPHORST, MC ;
BAKKER, O ;
WIERSINGA, WM .
JOURNAL OF ENDOCRINOLOGY, 1995, 146 (03) :475-483
[6]  
BOUABOULA M, 1992, J BIOL CHEM, V267, P21830
[7]   EXPRESSION OF THYROID-HORMONE RECEPTOR BETA-2 IN RAT HYPOTHALAMUS [J].
COOK, CB ;
KAKUCSKA, I ;
LECHAN, RM ;
KOENIG, RJ .
ENDOCRINOLOGY, 1992, 130 (02) :1077-1079
[8]   Fasting-induced increase in type II iodothyronine deiodinase activity and messenger ribonucleic acid levels is not reversed by thyroxine in the rat hypothalamus [J].
Diano, S ;
Naftolin, F ;
Goglia, F ;
Horvath, TL .
ENDOCRINOLOGY, 1998, 139 (06) :2879-2884
[9]   Type I interferons induce proteins susceptible to act as thyroid receptor (TR) corepressors and to signal the TR for destruction by the proteasome: possible etiology for unexplained chronic fatigue [J].
Englebienne, P ;
Verhas, M ;
Herst, CV ;
De Meirleir, K .
MEDICAL HYPOTHESES, 2003, 60 (02) :175-180
[10]   Lipopolysaccharide induces type 2 iodothyronine deiodinase in the mediobasal hypothalamus: Implications for the nonthyroidal illness syndrome [J].
Fekete, C ;
Gereben, B ;
Doleschall, M ;
Harney, JW ;
Dora, JM ;
Bianco, AC ;
Sarkar, S ;
Liposits, Z ;
Rand, W ;
Emerson, C ;
Kacskovics, I ;
Larsen, PR ;
Lechan, RM .
ENDOCRINOLOGY, 2004, 145 (04) :1649-1655