Faulty serotonin - DHEA interactions in autism: results of the 5-hydroxytryptophan challenge test

被引:1
作者
Croonenberghs, Jan [1 ]
Spaas, Kristien [1 ]
Wauters, Annick [2 ]
Verkerk, Robert [3 ]
Scharpe, Simon [3 ]
Deboutte, Dirk [1 ]
Maes, Michael [4 ]
机构
[1] Univ Antwerp, Fac Med, AZ Middelheim, Univ Ctr Child & Adolescent Psychiat, B-2020 Antwerp, Belgium
[2] AZ Middelheim, Lab Clin Biol, Antwerp, Belgium
[3] Univ Antwerp, Dept Med Biochem, Edegem, Belgium
[4] Clin Res Ctr Mental Hlth, Antwerp, Belgium
关键词
autism; serotonin; cortisol; DHEA; L-5-hydroxytryptophan; neurogenesis; neurodegeneration; neurotoxic; stress;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Autism is accompanied by peripheral and central disorders in the metabolism of serotonin (5-HT). The present study examines plasma dehydroepiandrosterone-sulphate (DHEA-S) and the cortisol/DHEA-S ratio following administration of L-5-hydroxytryptophan (5-HTP), the direct precursor of 5-HT, to autistic patients. METHODS: Plasma DHEA-S levels were determined both before and after administration of 5-HTP or placebo, on two consecutive days in a single blind order in 18 male autistic patients and 22 matched healthy controls. RESULTS: The 5-HTP-induced DHEA-S responses were significantly higher in autistic patients than in controls. In baseline conditions, the cortisol/DHEA-S ratio was significantly higher in autistic patients than in controls. Discussion: The results suggest that autism is accompanied by a major disequilibrium in the serotonergic system. The increased Cortisol (neurotoxic) versus DHEA-S (neuroprotective) ratio suggests that an increased neurotoxic potential occurs in autism. CONCLUSIONS: It is concluded that a disequilibrium in the peripheral and central turnover of serotonin and an increased neurotoxic capacity by glucocorticoids are important pathways in autism.
引用
收藏
页码:385 / 390
页数:6
相关论文
共 45 条
[1]  
Achenbach T., 1991, Manual for the youth self-report and 1991 profile
[2]  
Achenbach T. M., MANUAL CHILD BEHAV C
[3]  
AMAN MG, 1994, ASSESSMENT REHABILIT, V1, P1
[4]   Dehydroepiandrosterone (DHEA) protects hippocampal cells from oxidative stress-induced damage [J].
Bastianetto, S ;
Ramassamy, C ;
Poirier, J ;
Quirion, R .
MOLECULAR BRAIN RESEARCH, 1999, 66 (1-2) :35-41
[5]  
Baulieu EE, 1996, J ENDOCRINOL, V150, pS221
[6]   Neurosteroids: A novel function of the brain [J].
Baulieu, EE .
PSYCHONEUROENDOCRINOLOGY, 1998, 23 (08) :963-987
[7]   Dehydroepiandrosterone protects hippocampal neurons against neurotoxin-induced cell death: Mechanism of action [J].
Cardounel, A ;
Regelson, W ;
Kalimi, M .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 222 (02) :145-149
[8]  
COHEN DJ, 1974, ARCH GEN PSYCHIAT, V31, P845
[9]   Dehydroepiandrosterone: A potential signalling molecule for neocortical organization during development [J].
Compagnone, NA ;
Mellon, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (08) :4678-4683
[10]  
Cook Edwin H. Jr., 1996, Current Opinion in Pediatrics, V8, P348, DOI 10.1097/00008480-199608000-00008