Behavioral and neurotoxic effects seen during and after subchronic exposure of rats to organic mercury

被引:11
作者
Vezér, T
Papp, A
Kurunczi, A
Párducz, A
Náray, M
Nagymajtényi, L
机构
[1] Univ Szeged, Dept Publ Hlth, H-6720 Szeged, Hungary
[2] Hungarian Acad Sci, Biol Res Ctr, H-6701 Szeged, Hungary
[3] Natl Ctr Publ Hlth, Budapest, Hungary
关键词
methyl mercury; spontaneous exploratory activity; psychomotor performance; electrocorticogram; evoked activity; rat;
D O I
10.1016/j.etap.2004.12.045
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Young adult male Wistar rats (24/group) were treated for 5 weeks with methyl mercury(II)chloride (corresponding to 0.5 and 2.0 mgHg degrees/kg b.w., control: distilled water) by gavage, followed by a 19 weeks post-treatment period. Spontaneous motility, psychomotor performance and sensorimotor gating was repeatedly tested, electrophysiological recordings done, in the rats throughout the whole experiment. Decreased horizontal open field activity, reduced number of "noise positive" startle responses, as well as increase of startle response onset latency and peak time, and decrease of peak amplitude, was seen in the treated animals. Most changes disappeared in the post-treatment period. In the spontaneous cortical and hippocampal activity, altered distribution of the frequency bands was seen after 5 weeks of treatment but not at the end of the post-treatment period. Hippocampal population spikes in the treated animals were depressed and showed less potentiation, which effect was still present 19 weeks after finishing the treatment. The duration of the sensory cortical evoked potentials was shorter than in the controls. In the treated rats, tyrosine hydroxylase-immunoreactive boutons in the substantia nigra pars reticulata were shrunk; blood and brain Hg levels were significantly higher and decreased only slowly. Considering the continuous presence of low levels of mercurials in the human environment, effects of this kind may be supposed as the background of some human neurobehavioral abnormalities. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:785 / 796
页数:12
相关论文
共 47 条
[11]   Effects of chronic low-level oral lead exposure on prepulse inhibition of acoustic startle in the rat [J].
Commissaris, RL ;
Tavakoli-Nezhad, M ;
Barron, AJ ;
Pitts, DK .
NEUROTOXICOLOGY AND TERATOLOGY, 2000, 22 (01) :55-60
[12]  
Counter SA, 1998, NEUROTOXICOLOGY, V19, P185
[13]  
Denny MF, 1996, NEUROTOXICOLOGY, V17, P47
[14]   Electrophysiological biomarkers of an organophosphorous pesticide, dichlorvos [J].
Dési, I ;
Nagymajtényi, L .
TOXICOLOGY LETTERS, 1999, 107 (1-3) :55-64
[15]   5-HT1B receptor knockout, but not 5-HT1A receptor knockout mice, show reduced startle reactivity and footshock-induced sensitization, as measured with the acoustic startle response [J].
Dirks, A ;
Pattij, T ;
Bouwknecht, JA ;
Westphal, TT ;
Hijzen, TH ;
Groenink, L ;
van der Gugten, J ;
Oosting, RS ;
Hen, R ;
Geyer, MA ;
Olivier, B .
BEHAVIOURAL BRAIN RESEARCH, 2001, 118 (02) :169-178
[16]   Mechanism of action of methylmercury on in vivo striatal dopamine release -: Possible involvement of dopamine transporter [J].
Faro, LRF ;
do Nascimento, JLM ;
Alfonso, M ;
Durán, R .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (05) :455-465
[17]   Protection of methylmercury effects on the in vivo dopamine release by NMDA receptor antagonists and nitric oxide synthase inhibitors [J].
Faro, LRF ;
do Nascimento, JLM ;
Alfonso, M ;
Durán, R .
NEUROPHARMACOLOGY, 2002, 42 (05) :612-618
[18]   Effects of methyl mercury on the in vivo release of dopamine and its acidic metabolites DOPAC and HVA from striatum of rats [J].
Faro, LRF ;
Duran, R ;
do Nascimento, JLM ;
Alfonso, M ;
Picano-Diniz, CW .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 1997, 38 (02) :95-98
[19]   CHOLINERGIC MECHANISMS IN LEARNING, MEMORY AND DEMENTIA - A REVIEW OF RECENT-EVIDENCE [J].
FIBIGER, HC .
TRENDS IN NEUROSCIENCES, 1991, 14 (06) :220-223
[20]   Prenatal coexposure to metallic mercury vapour and methylmercury produce interactive behavioural changes in adult rats [J].
Fredriksson, A ;
Dencker, L ;
Archer, T ;
Danielsson, BRG .
NEUROTOXICOLOGY AND TERATOLOGY, 1996, 18 (02) :129-134