Arylalkylamine N-acetyltransferase (AANAT) genotype as a personal trait in melatonin synthesis

被引:11
作者
Bloemeke, Brunhilde [1 ]
Golka, Klaus [2 ]
Griefahn, Barbara [2 ]
Roemer, Hermann C. [2 ]
机构
[1] Univ Trier, Dept Environm Toxicol, D-54296 Trier, Germany
[2] Univ Dortmund IfADo, Leibniz Res Ctr Working Environm & Human Factors, Inst Occupat Physiol, Dortmund, Germany
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | 2008年 / 71卷 / 13-14期
关键词
ETHNIC-DIFFERENCES; PINEAL-GLAND; SEROTONIN; RHYTHM; IDENTIFICATION; POLYMORPHISM; DISORDERS; GENE; NAT2;
D O I
10.1080/15287390801988020
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The melatonin rhythm is arguably the best marker for the phase of the endogenous "biological clock." Arylalkylamine N-acetyltransferase ( AANAT) is known to catalyze the acetylation of serotonin, a rate-limiting process in melatonin synthesis. Different single-nucleotide polymorphisms ( SNPs) in the AANAT gene were identified recently in the Japanese population, and one of the genes was significantly associated with the delayed sleep phase syndrome. Thus, 54 healthy Caucasian males were genotyped to investigate whether these SNPs in the AANAT gene affected melatonin levels. The endogenous melatonin levels were analyzed in saliva under standardized experimental conditions ("constant routines") by radioimmunoassay. Despite the broad temporal variation of the human nocturnal melatonin profiles, none of the investigated SNPs were found in the AANAT gene in this study. These findings point to ethnic differences with respect to these SNPs, rather than time of day termed "morningness." In summary, SNPs in the AANAT gene identified thus far cannot explain the observed interindividual differences for nocturnal melatonin profiles in the subjects investigated.
引用
收藏
页码:874 / 876
页数:3
相关论文
共 22 条
[1]  
Arendt J, 1998, REV REPROD, V3, P13, DOI 10.1530/revreprod/3.1.13
[2]  
Arendt J., 1995, MELATONIN MAMMALIAN
[3]   Identification of N-acetyltransferase 2 genotypes by continuous monitoring of fluorogenic hybridization probes [J].
Blömeke, B ;
Sieben, S ;
Spötter, D ;
Landt, O ;
Merk, HF .
ANALYTICAL BIOCHEMISTRY, 1999, 275 (01) :93-97
[4]  
BLOMEKE B, 1999, IARC SCI PUBL, V148, P133
[5]   A mathematical model of diurnal variations in human plasma melatonin levels [J].
Brown, EN ;
Choe, Y ;
Shanahan, TL ;
Czeisler, CA .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (03) :E506-E516
[6]   The human serotonin N-acetyltransferase (EC 2.3.1.87) gene (AANAT): Structure, chromosomal localization, and tissue expression [J].
Coon, SL ;
Mazuruk, K ;
Bernard, M ;
Roseboom, PH ;
Klein, DC ;
Rodriguez, IR .
GENOMICS, 1996, 34 (01) :76-84
[7]   Circadian rhythm sleep disorders (CRSD) [J].
Dagan, Y .
SLEEP MEDICINE REVIEWS, 2002, 6 (01) :45-55
[8]   Cytochrome P450 isoforms involved in melatonin metabolism in human liver microsomes [J].
Facciolá, G ;
Hidestrand, M ;
von Bahr, C ;
Tybring, G .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 56 (12) :881-888
[9]   The enhanced bladder cancer susceptibility of NAT2 slow acetylators towards aromatic amines: a review considering ethnic differences [J].
Golka, K ;
Prior, V ;
Blaszkewicz, M ;
Bolt, HM .
TOXICOLOGY LETTERS, 2002, 128 (1-3) :229-241
[10]   Occupational history and genetic N-acetyltransferase polymorphism in urothelial cancer patients of Leverkusen, Germany [J].
Golka, K ;
Prior, V ;
Blaszkewicz, M ;
Cascorbi, I ;
Schops, W ;
Kierfeld, G ;
Roots, I ;
Blot, HM .
SCANDINAVIAN JOURNAL OF WORK ENVIRONMENT & HEALTH, 1996, 22 (05) :332-338