EFFECTS OF SINGLE AND REPEATED FOOTSHOCK ON DOPAMINE RELEASE AND METABOLISM IN THE BRAINS OF FISCHER RATS

Citation
Sj. Chrapusta et al., EFFECTS OF SINGLE AND REPEATED FOOTSHOCK ON DOPAMINE RELEASE AND METABOLISM IN THE BRAINS OF FISCHER RATS, Journal of neurochemistry, 68(5), 1997, pp. 2024-2031
Citations number
52
Categorie Soggetti
Biology,Neurosciences
Journal title
ISSN journal
00223042
Volume
68
Issue
5
Year of publication
1997
Pages
2024 - 2031
Database
ISI
SICI code
0022-3042(1997)68:5<2024:EOSARF>2.0.ZU;2-F
Abstract
Changes in the tissue levels of 3-methoxytyramine (3-MT), 3,4-dihydrox yphenylacetic acid (DOPAC), homovanillic acid (HVA), and dopamine in t he frontal cortex, hypothalamus, nucleus accumbens, and striatum were evaluated after 0.5-4 h of footshock (2 mA, for 3 s every 30 +/- 5 s) in Fischer rats. 3-MT, DOPAC, and HVA levels in the four brain areas p eaked at 0.5 h and in most cases returned to baseline values within 4 h. No changes were found in dopamine levels. Repeated footshock stress was evaluated by administering 10 footshock sessions (0.5 h, two per day for 5 days). At the end of the 10th footshock session, 3-MT levels were higher than at the end of the first footshock session in three o f the four brain regions, indicating sensitization of dopamine release . No differences were found between the first and 10th footshock sessi ons in DOPAC and HVA levels. Fourteen days after the 10th footshock se ssion, the levels of 3-MT, DOPAC, and HVA were the same as in control rats in all four brain regions, A 0.5-h footshock challenge presented 14 days after the 10th footshock session attenuated DOPAC levels in th e hypothalamus and nucleus accumbens, In contrast, DOPAC and HVA level s in the frontal cortex showed sensitization after footshock challenge , and a similar trend was apparent for 3-MT levels, These results indi cate that repeated footshock stress induces generalized sensitization of dopamine release and turnover in some areas of the brain of Fischer rats. This sensitization may persist in the cortical but not subcorti cal dopamine neurons after discontinuation of the treatment.