| Autor: |
Moreira KM; Psychobiology Department, Universidade Federal de São Paulo (UNIFESP), Rua Napoleão de Barros 925, São Paulo 04024-002, SP, Brazil., Hipólide DC, Nobrega JN, Bueno OF, Tufik S, Oliveira MG |
| Jazyk: |
angličtina |
| Zdroj: |
Brain research [Brain Res] 2003 Jul 04; Vol. 977 (1), pp. 31-7. |
| DOI: |
10.1016/s0006-8993(03)02688-x |
| Abstrakt: |
Previous work had indicated that animals that were sleep-deprived and then trained on a passive avoidance task show poor retention of the task 24 h later after being allowed to sleep freely again. Cholinergic involvement is suggested by the fact that this effect is prevented by treatment with the muscarinic agonist pilocarpine during sleep deprivation. The observation that similar deficits are observed in non-deprived rats after treatment with M1-selective antagonist compounds such as dicyclomine or pirenzepine cause similar impairments, and gave rise to the hypothesis that sleep deprivation might induce significant reductions in M1 binding in brain areas involved in learning and memory processes. Rats were deprived of sleep for 96 h and then either immediately killed, or allowed to recover sleep for 24 h before being killed. [3H]pirenzepine binding to M1 sites was examined by quantitative autoradiography in 39 different brain areas in cage controls, sleep-deprived and sleep-recovered animals (N=8 per group). No significant differences among groups were found in any brain region. A separate group of animals was subjected to the sleep deprivation procedure and then trained in a simple avoidance task. Animals were then allowed to sleep and retested 24 h later. This group showed a significant impairment in the avoidance task compared to cage controls, in agreement with previous observations. These data suggest that proactive learning/memory deficits induced by sleep deprivation cannot be attributed to altered M1 binding either immediately after deprivation (when avoidance training occurs) or after sleep has recovered (when acquisition/retention are tested). The possibility remains that alterations in M1 function occur at post-membrane second messenger systems. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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