Prenatal exposure to methylmercury changes dopamine-modulated motor activity during early ontogeny:: age and gender-dependent effects

被引:71
作者
Giménez-Llort, L
Ahlbom, E
Daré, E
Vahter, M
Ögren, SO
Ceccatelli, S [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Div Toxicol & Neurotoxicol, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden
[3] Karolinska Inst, Inst Environm Med, Div Met Toxicol, S-17177 Stockholm, Sweden
关键词
methylmercury; motor activity; dopamine D-2 receptor; male and female rats;
D O I
10.1016/S1382-6689(00)00060-0
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We have shown previously that prenatal exposure of rats to 0.5 mg/kg/day of methylmercury (MeHg) produces gender-dependent changes in motor activity in adulthood. In the present study we have investigated whether changes in motor activity could also be found during early ontogeny of the offspring. Pregnant rats were treated with MeHg from day 7 of pregnancy to day 7 of lactation. The habituation to a novel environment (spontaneous activity) and the response to stimulation of the dopaminergic system were studied on postnatal day 14 and 21. Measures of spontaneous activity showed a slight increase in MeHg-prenatal exposed male and female rats at 14 days, but not at 21 days. Following administration of U91356A, a selective dopamine D-2 receptor agonist, a significantly lower dopamine-mediated locomotor activity was observed in the 21 day old MeHg-treated males, but not in females. These results show that prenatal exposure to MeHg alters postjunctional dopaminergic activity during the period of maturation of the dopamine system in the brain. Moreover, the gender-dependent susceptibility previously found in adulthood is already evident at the prepubertal stage. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:61 / 70
页数:10
相关论文
共 61 条
[41]  
OGREN SO, 1979, DOPAMINERGIC ERGOT D, P187
[42]  
Palkovits M, 1988, MAPS GUIDE MICRODISS
[43]   Pharmacology of U-91356A, an agonist for the dopamine D-2 receptor subtype [J].
Piercey, MF ;
Moon, MW ;
Sethy, VH ;
Schreur, PJKD ;
Smith, MW ;
Tang, AH ;
VonVoigtlander, PF .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 317 (01) :29-38
[44]   ONTOGENY OF DOPAMINE D1 AND D2 RECEPTOR SUBTYPES IN RAT BASAL GANGLIA - A QUANTITATIVE AUTORADIOGRAPHIC STUDY [J].
RAO, PA ;
MOLINOFF, PB ;
JOYCE, JN .
DEVELOPMENTAL BRAIN RESEARCH, 1991, 60 (02) :161-177
[45]  
Rice DC, 1996, NEUROTOXICOLOGY, V17, P139
[46]   BRAIN AND TISSUE-LEVELS OF MERCURY AFTER CHRONIC METHYLMERCURY EXPOSURE IN THE MONKEY [J].
RICE, DC .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1989, 27 (02) :189-198
[47]  
Rossi A., 1996, THESIS KAROLINSKA I
[48]   Prenatal exposure to methylmercury alters locomotor activity of male but not female rats [J].
Rossi, AD ;
Ahlbom, E ;
Ögren, SO ;
Nicotera, P ;
Ceccatelli, S .
EXPERIMENTAL BRAIN RESEARCH, 1997, 117 (03) :428-436
[49]   PSYCHOPHARMACOLOGICAL EFFECTS OF LOW AND HIGH-DOSES OF APOMORPHINE DURING ONTOGENY [J].
SHALABY, IA ;
SPEAR, LP .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1980, 67 (04) :451-459
[50]  
SHIMAI S, 1985, Journal of Toxicological Sciences, V10, P199