Overexpression of corticotropin-releasing hormone in transgenic mice and chronic stress-like autonomic and physiological alterations

被引:70
作者
Dirks, A [1 ]
Groenink, L
Bouwknecht, JA
Hijzen, TH
van der Gugten, J
Ronken, E
Verbeek, JS
Veening, JG
Dederen, PJWC
Korosi, A
Schoolderman, LF
Roubos, EW
Olivier, B
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Psychopharmacol, Utrecht, Netherlands
[2] Solvay Pharmaceut, Dept CNS Pharmacol, Weesp, Netherlands
[3] Leiden Univ, Med Ctr, Dept Human & Clin Genet, Leiden, Netherlands
[4] UMC St Radboud, Dept Anat, Nijmegen, Netherlands
[5] Univ Nijmegen, Fac Sci, Dept Cellular Anim Physiol, Nijmegen, Netherlands
[6] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
关键词
body temperature; chronic stress; CRF; CRH; food intake; heart rate; mice; quantitative immunocytochemistry; radiotelemetry;
D O I
10.1046/j.1460-9568.2002.02245.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To gain a greater insight into the relationship between hyperactivity of the corticotropin-releasing hormone (CRH) system and autonomic and physiological changes associated with chronic stress, we developed a transgenic mouse model of central CRH overproduction. The extent of central and peripheral CRH overexpression, and the amount of bioactive CRH in the hypothalamus were determined in two lines of CRH-overexpressing (CRH-OE) mice. Furthermore, 24 h patterns of body temperature, heart rate, and activity were assessed using radiotelemetry, as well as cumulative water and food consumption and body weight gain over a 7-day period. CRH-OE mice showed increased amounts of CRH peptide and mRNA only in the central nervous system. Despite the presence of the same CRH transgene in their genome, only in one of the two established lines of CRH-OE mice ( line 2122, but not 2123) was overexpression of CRH associated with increased levels of bioactive CRH in the hypothalamus, increased body temperature and heart rate ( predominantly during the light ( inactive) phase of the diurnal cycle), decreased heart rate variability during the dark ( active) phase, and increased food and water consumption, when compared with littermate wildtype mice. Because line 2122 of the CRH transgenic mice showed chronic stress-like neuroendocrine and autonomic changes, these mice appear to represent a valid animal model for chronic stress and might be valuable in the research on the consequences of CRH excess in situations of chronic stress.
引用
收藏
页码:1751 / 1760
页数:10
相关论文
共 71 条
[61]   DEVELOPMENT OF CUSHINGS-SYNDROME IN CORTICOTROPIN-RELEASING FACTOR TRANSGENIC MICE [J].
STENZELPOORE, MP ;
CAMERON, VA ;
VAUGHAN, J ;
SAWCHENKO, PE ;
VALE, W .
ENDOCRINOLOGY, 1992, 130 (06) :3378-3386
[62]  
STENZELPOORE MP, 1994, J NEUROSCI, V14, P2579
[63]   Effect of tone-dependent fear conditioning on heart rate and behavior of C57BL/6N mice [J].
Stiedl, O ;
Spiess, J .
BEHAVIORAL NEUROSCIENCE, 1997, 111 (04) :703-711
[64]   CORTICOTROPIN RELEASING-FACTOR PRODUCES BEHAVIORAL ACTIVATION IN RATS [J].
SUTTON, RE ;
KOOB, GF ;
LEMOAL, M ;
RIVIER, J ;
VALE, W .
NATURE, 1982, 297 (5864) :331-333
[65]   RAT CORTICOTROPIN-RELEASING HORMONE GENE - SEQUENCE AND TISSUE-SPECIFIC EXPRESSION [J].
THOMPSON, RC ;
SEASHOLTZ, AF ;
HERBERT, E .
MOLECULAR ENDOCRINOLOGY, 1987, 1 (05) :363-370
[66]   CHARACTERIZATION OF A 41-RESIDUE OVINE HYPOTHALAMIC PEPTIDE THAT STIMULATES SECRETION OF CORTICOTROPIN AND BETA-ENDORPHIN [J].
VALE, W ;
SPIESS, J ;
RIVIER, C ;
RIVIER, J .
SCIENCE, 1981, 213 (4514) :1394-1397
[67]   PHYSIOLOGICAL-ROLE OF CORTICOTROPIN-RELEASING FACTOR IN THE CONTROL OF ADRENOCORTICOTROPIN-MEDIATED CORTICOSTERONE RELEASE FROM THE RAT ADRENAL-GLAND [J].
VANOERS, JWAM ;
HINSON, JP ;
BINNEKADE, R ;
TILDERS, FJH .
ENDOCRINOLOGY, 1992, 130 (01) :282-288
[68]   THE CONTINUING PROBLEM OF FALSE POSITIVES IN REPEATED MEASURES ANOVA IN PSYCHOPHYSIOLOGY - A MULTIVARIATE SOLUTION [J].
VASEY, MW ;
THAYER, JF .
PSYCHOPHYSIOLOGY, 1987, 24 (04) :479-486
[69]   Patterns of c-fos expression induced by fluvoxamine are different after acute vs. chronic oral administration [J].
Veening, JG ;
Coolen, LM ;
Spooren, WJPM ;
Joosten, H ;
van Oorschot, R ;
Mos, J ;
Ronken, E ;
Olivier, B .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 1998, 8 (03) :213-226
[70]   TISSUE-SPECIFIC CONTROL ELEMENTS OF THE THY-1 GENE [J].
VIDAL, M ;
MORRIS, R ;
GROSVELD, F ;
SPANOPOULOU, E .
EMBO JOURNAL, 1990, 9 (03) :833-840