1989
DOI: 10.1016/0197-4580(89)90028-6
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Septo-hippocampal neurons in the aged rat: Relation between their electrophysiological and pharmacological properties and behavioral performances

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Cited by 37 publications
(15 citation statements)
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“…The type 1 theta requires a connection to the isocortex via the entorhinal cortex, rather than depending on a particular neurotransmitter system [26]. A few reports have described changes in rat hippocampal theta with aging [13,16], however, the correlation between the two types of related behavior because it is a simple behavior to distinguish from LIA related behavior, such as immobility. The type 1 theta recordings from the walking rats were sampled and analyzed (Fig.…”
Section: Methodsmentioning
confidence: 98%
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“…The type 1 theta requires a connection to the isocortex via the entorhinal cortex, rather than depending on a particular neurotransmitter system [26]. A few reports have described changes in rat hippocampal theta with aging [13,16], however, the correlation between the two types of related behavior because it is a simple behavior to distinguish from LIA related behavior, such as immobility. The type 1 theta recordings from the walking rats were sampled and analyzed (Fig.…”
Section: Methodsmentioning
confidence: 98%
“…Therefore age-related impairment of these functions might be due at least in part to alterations in the hippocampus. The morphological and neurochemical age-related changes in rat hippocampus are well documented [3,4,8,9,14,15,22,23,30], but fewer studies have examined the age-related changes in electrophysiological properties [13,15,16,19,21].…”
Section: Methodsmentioning
confidence: 99%
“…These deficits were reminiscent of those produced by the nonselective muscarinic antagonist scopolamine or by ligands that impair cognition by dysregulating cholinergic neurotransmission at the level of the septohippocampal pathway. [42][43][44][45]49,50 Dysregulated acetylcholine release in response to environmental stimuli and deficits in the passive avoidance paradigm are not likely to be because of nonspecific phenotypic alterations such as hyperlocomotion in the KO mice. In fact, M4-KO mice that display increased basal locomotor activity 9 do not show deficits in the passive avoidance, whereas M2-KO mice, that perform poorly in the passive avoidance test, display normal locomotor activity (unpublished observations).…”
Section: Discussionmentioning
confidence: 99%
“…Although the passive avoidance paradigm is a nonspecific aversive memory test that involves a number of brain structures, it exhibits well-documented validity in depicting memory impairments as a result of aging, or pharmacological and genetic manipulations. [42][43][44][45][46] Acquisition and/or retention in the passive avoidance test are dependent on the integrity of the hippocampal cholinergic pathway. 35,[42][43][44]47,48 M2-and M2/M4-KO mice, but not M4-KO mice, showed impaired memory retention in the passive avoidance paradigm.…”
Section: Discussionmentioning
confidence: 99%
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