Posttraining Inactivation of Excitatory Afferent Input to the Locus Coeruleus Impairs Retention in an Inhibitory Avoidance Learning Task
Posttraining Inactivation of Excitatory Afferent Input to the Locus Coeruleus Impairs Retention in an Inhibitory Avoidance Learning Task
复制标题
训练后蓝斑兴奋性传入输入失活会损害抑制性回避学习任务的记忆力
DOI:
--
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发表时间:
2000
影响因子:
2.7
通讯作者:
Cedric L. Williams
中科院分区:
文献类型:
--
作者:
E. Clayton;Cedric L. Williams
These experiments examined whether the nucleus paragigantocellularis (PGi) contributes to memory storage processing via its ascending excitatory influence on locus coeruleus (LC) neuronal activity. Activation of the LC leads to memory enhancement and also results in a widespread release of norepinephrine in target structures, such as the amygdala and hippocampus. Infusion of norepinephrine into either structure also improves memory for several types of learned responses. Thus, the capacity for norepinephrine to modulate memory within limbic structures may be contingent upon the functional connections between PGi and the LC. To examine this hypothesis, male Sprague-Dawley rats were implanted with cannula aimed above PGi (Experiments 1 and 2) or 1.5 mm dorsal or medial to PGi (Experiment 3). Immediately following inhibitory avoidance training (0.45 mA, 0. 5 s), phosphate-buffered saline, lidocaine (Experiment 1), or 12.5 or 25 nmol/0.5 microl of the GABA agonist muscimol (Experiment 2) was infused into PGi. On a retention test given 48 h later, the latency to reenter the footshock compartment was significantly shorter for subjects given either lidocaine or 12.5 or 25.0 nmol of muscimol compared to controls. In Experiment 3, infusion of lidocaine or muscimol into areas 1.5 mm dorsal or medial to PGi did not significantly alter retention, indicating that the memory impairment observed in Experiments 1 and 2 was site specific and not due to the spread of drug to cell groups surrounding PGi. These findings suggest that PGi may serve a vital function in relaying biologically relevant information to forebrain structures involved in memory via its excitatory influence on the LC.
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影响因子:
--
作者:
Gary Aston-Jones;C. Chiang;T. Alexinsky
通讯作者:
Gary Aston-Jones;C. Chiang;T. Alexinsky
影响因子:
1.9
作者:
Williams,CL;McGaugh,JL
通讯作者:
McGaugh,JL
DOI:
10.1152/ajpregu.1985.249.6.r672
发表时间:
1985
期刊:
The American journal of physiology
影响因子:
--
作者:
Sun,MK;Guyenet,PG
通讯作者:
Guyenet,PG
影响因子:
56.9
作者:
ASTONJONES, G;ENNIS, M;SHIPLEY, MT
通讯作者:
SHIPLEY, MT