Chronic stress induces impairment of spatial working memory because of prefrontal dopaminergic dysfunction

Citation
K. Mizoguchi et al., Chronic stress induces impairment of spatial working memory because of prefrontal dopaminergic dysfunction, J NEUROSC, 20(4), 2000, pp. 1568-1574
Citations number
58
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROSCIENCE
ISSN journal
02706474 → ACNP
Volume
20
Issue
4
Year of publication
2000
Pages
1568 - 1574
Database
ISI
SICI code
0270-6474(20000215)20:4<1568:CSIIOS>2.0.ZU;2-X
Abstract
Although the mechanism responsible for cognitive deficits in stress-related neuropsychiatric disorders has been obscure, prefrontal cortical (PFC) dop aminergic dysfunction is thought to be involved. In animals, the mesoprefro ntal dopaminergic system is particularly vulnerable to stress, and chronic stress induces working memory impairment. However, the relation between the working memory impairment and altered dopaminergic activity in chronically stressed rats is unclear. Furthermore, the change of dopaminergic activity in the PFC induced by stress is thought to express as a stress response, n ot as a disorder of organic function. We have previously reported that chro nic stress administered by water immersion and restraint for 4 weeks induce s a organic disorder such as hippocampal neuronal degeneration. We therefor e examined whether chronically stressed (4 weeks) and recovered (10 d) rats show a working memory impairment caused by reduced dopamine (DA) transmiss ion in the PFC, as suspected in the neuropsychiatric disorders. The stress impaired the spatial working memory evaluated by T-maze task and induced a marked reduction of DA transmission concomitant with an increase in DA D1 r eceptor density in the PFC. This memory impairment was sufficiently amelior ated by intra-PFC infusion of 10 ng SKF 81297, a D1 receptor-specific agoni st. Pretreatment with intraperitoneal injection of 20 mg/kg SCH 23390, a D1 receptor antagonist, reversed the SKF 81297 response. These results indica te that chronic stress induces working memory impairment through a D1 recep tor-mediated hypodopaminergic mechanism in the PFC. These findings provide important information for understanding of the mechanisms underlying PFC dy sfunction in stress-related neuropsychiatric disorders.