Blunted ACTH and cortisol responses to systemic injection of corticotropin-releasing hormone (CRH) in fibromyalgia role of somatostatin and CRH-binding protein

被引:32
作者
Riedel, W [1 ]
Schlapp, U
Leck, S
Netter, P
Neeck, G
机构
[1] Max Planck Inst Physiol & Clin Res, WG Kerckhoff Inst, D-61231 Bad Nauheim, Germany
[2] Univ Giessen, Inst Psychol, D-35390 Giessen, Germany
[3] WG Kerckhoff Clin & Fdn, Dept Rheumatol, Bad Nauheim, Germany
来源
NEUROENDOCRINE IMMUNE BASIS OF THE RHEUMATIC DISEASES II, PROCEEDINGS | 2002年 / 966卷
关键词
ACTH; cortisol; corticotropin-releasing hormone; fibromyalgia; somatostatin; CRH-binding protein;
D O I
10.1111/j.1749-6632.2002.tb04251.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thirteen female patients suffering from fibromyalgia (FM) and thirteen female age-matched controls were intravenously injected with a bolus dose of 100 mug corticotropin-releasing hormone (CRH), and the evoked secretion pattern of ACTH, cortisol, somatostatin, and growth hormone (GH) was followed up for two hours, together with the plasma levels of CRH. The increases of ACTH and cortisol following CRH were not significantly different between controls and FM patients. The increase of plasma CRH following its injection was significantly higher in FM patients and lasted about 45 min, paralleled by an increase of somatostatin with a similar time course. Basal GH levels were significantly lower in FM patients. GH increased in FM patients 90 min after injection of CRH, coincident with decreasing CRH and somatostatin levels, while GH levels in controls rather decreased with the lowest values occurring 90 min after CRH. The results support the concept that the hormonal secretion pattern frequently observed in FM patients is primarily caused by CRH, possibly as a response to chronic pain and stress. The elevated levels of CRH in the circulation of FM patients suggest elevated levels of CRH-binding protein, which could explain why the levels of ACTH and cortisol between controls and FM following CRH do not differ.
引用
收藏
页码:483 / 490
页数:8
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共 33 条
[2]   PERIPHERAL BUT NOT INTRACEREBROVENTRICULAR CORTICOTROPIN-RELEASING HORMONE (CRH) PRODUCES ANTINOCICEPTION WHICH IS NOT OPIOID MEDIATED [J].
AYESTA, FJ ;
NIKOLARAKIS, KE .
BRAIN RESEARCH, 1989, 503 (02) :219-224
[3]   LOW-LEVELS OF SOMATOMEDIN C IN PATIENTS WITH THE FIBROMYALGIA SYNDROME - A POSSIBLE LINK BETWEEN SLEEP AND MUSCLE PAIN [J].
BENNETT, RM ;
CLARK, SR ;
CAMPBELL, SM ;
BURCKHARDT, CS .
ARTHRITIS AND RHEUMATISM, 1992, 35 (10) :1113-1116
[4]   THE CONCEPTS OF STRESS AND STRESS SYSTEM DISORDERS - OVERVIEW OF PHYSICAL AND BEHAVIORAL HOMEOSTASIS [J].
CHROUSOS, GP ;
GOLD, PW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 267 (09) :1244-1252
[5]   HYPOTHALAMIC-PITUITARY-ADRENAL AXIS PERTURBATIONS IN PATIENTS WITH FIBROMYALGIA [J].
CROFFORD, LJ ;
PILLEMER, SR ;
KALOGERAS, KT ;
CASH, JM ;
MICHELSON, D ;
KLING, MA ;
STERNBERG, EM ;
GOLD, PW ;
CHROUSOS, GP ;
WILDER, RL .
ARTHRITIS AND RHEUMATISM, 1994, 37 (11) :1583-1592
[6]   Evidence that abnormalities of central neurohormonal systems are key to understanding fibromyalgia and chronic fatigue syndrome [J].
Crofford, LJ ;
Demitrack, MA .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 1996, 22 (02) :267-&
[7]   Neurohormonal perturbations in fibromyalgia [J].
Crofford, LJ ;
Engleberg, NC ;
Demitrack, MA .
BAILLIERES CLINICAL RHEUMATOLOGY, 1996, 10 (02) :365-378
[8]   The somatostatin analogue octreotide modulates iodothyronine deiodinase activity and pituitary neuromedin B [J].
Curty, FH ;
Lisbôa, PC ;
Ortiga-Carvalho, TM ;
Pazos-Moura, CC .
THYROID, 2000, 10 (08) :647-652
[9]   HALF-TIME OF ENDOGENOUS GROWTH-HORMONE (GH) DISAPPEARANCE IN NORMAL MAN AFTER STIMULATION OF GH SECRETION BY GH-RELEASING HORMONE AND SUPPRESSION WITH SOMATOSTATIN [J].
FARIA, ACS ;
VELDHUIS, JD ;
THORNER, MO ;
VANCE, ML .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (03) :535-541
[10]   PHYSIOLOGICAL-ROLE OF SOMATOSTATIN IN CONTROL OF GROWTH-HORMONE AND THYROTROPIN SECRETION [J].
FERLAND, L ;
LABRIE, F ;
JOBIN, M ;
ARIMURA, A ;
SCHALLY, AV .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1976, 68 (01) :149-156