Effects of copper metabolism on neurological functions in Wistar and Wilson’s disease model rats

Behavioral functions of Wistar and Long-Evans Cinnamon (LEC) rats, Wilson’s disease animal model, were compared by measuring the open-field, acoustic startle reflex and prepulse inhibition (PPI), and shuttle-box avoidance learning tests with or without oral supplementation with copper or d-penicilla...

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Published inBiochemical and biophysical research communications Vol. 349; no. 3; pp. 1079 - 1086
Main Authors Fujiwara, Noriko, Iso, Hiroyuki, Kitanaka, Nobue, Kitanaka, Junichi, Eguchi, Hironobu, Ookawara, Tomomi, Ozawa, Keiichiro, Shimoda, Shigero, Yoshihara, Daisaku, Takemura, Motohiko, Suzuki, Keiichiro
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 27.10.2006
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Summary:Behavioral functions of Wistar and Long-Evans Cinnamon (LEC) rats, Wilson’s disease animal model, were compared by measuring the open-field, acoustic startle reflex and prepulse inhibition (PPI), and shuttle-box avoidance learning tests with or without oral supplementation with copper or d-penicillamine, copper chelator. All of the LEC rats, irrespective of the treatment, exhibited higher locomotor activity, a decreased habituation to startle response or a lower PPI, compared with Wistar rats. The copper content of all brain regions examined, except for the medulla oblongata of LEC rats, was significantly lower than those in Wistar rats. Besides, in the region of the striatum and the nucleus accumbens of the LEC rats, lower content of norepinephrine, and higher content of dopamine and serotonin were observed compared with Wistar rats. Although copper supplementation did not affect the brain copper content, it reduced the PPI in both Wistar and LEC rats. In contrast, d-penicillamine supplementation decreased both the brain copper content and locomotor activity, and enhanced the startle amplitude only in Wistar rats. These findings suggest that an imbalance in copper homeostasis affects monoamine metabolism and behavioral functions.
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ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2006.08.139