ORIGINAL RESEARCH
Effect of Organic Mercury Exposure
During Early Stage of Ontogenic Development
on the Central Dopaminergic System in Adult
Rats
A. Durczok, R. Szkilnik, R. Brus, P. Nowak, Ł. Labus, J. Konecki1, 1. K. Drabek,
1. G. Kuballa, 1. W. Rycerski, 2. K. Mengel
More details
Hide details
Department of Pharmacology and 1. Department of Histology and Embriology,
Medical University of Silesia, 41-808 Zabrze, H. Jordana 38, Poland
2. Department of Pharmacology, Institut of Pharmacology and Toxicology, University of Heidelberg,
68169 Mannheim, Germany
Pol. J. Environ. Stud. 2002;11(4):307-314
KEYWORDS
ABSTRACT
Organic mercury (CH3HgCl) with metal concentration 5 ppm in tap water was applied to rats suckling
their newborn for the first 21 days of life. A second group of young rats took the mercury in their tap water
5 ppm from the 22nd to the 43rd day of postnatal life. Control rats drank tap water only. In 2-month-old
male rats the following behavioral study was performed after saline or specific central dopamine receptor
agonists and agonists apply (quinpirole, SKF-38393, haloperidol, SCH-23390): irritability, yawning behavior,
oral activity, locomotion, exploratory activity, and catalepsy. In the striatum and frontal cortex of three
examined groups the biogenic amines levels (DA, DOPAC, HVA, 3-MT, 5-HT, 5-HIAA, NA) were estimated
by means of HPLC/ED technique, and DA and 5-HT turnover.
The effect of quinpirole (a central dopamine D2 receptor agonists) was also examined on (3H)glucose uptake
in discrete parts of the brain. It was shown that mercury affected behavioral changes after dopaminergic
agents apply to adult animals when exposed in the period from the 22nd to 43rd day of postnatal development.
Biochemical changes (biogenic amines level, turnover and (3H)glucose uptake) were more pronounced
in adult animals exposed to mercury via mother's milk (1st to 21st day of life). In light of the above
we conclude that early postnatal exposure of rats to organic mercury modulates activity of the central
dopamine neurotransmitter system.