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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 67 (1987), S. 77-84 
    ISSN: 1432-1106
    Keywords: Sympatho-hippocampal sprouting ; Mossy fibers ; Medial septum ; Hippocampus ; Zinc ; Noradrenergic system ; NGF
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Deafferentation of septo-hippocampal projections results in sprouting of sympathetic noradrenergic (NA) fibers into the hippocampus. To determine whether dentate granule cells are necessary for the initiation and/or direction of this sprouting, both NA intensity and zinc density were microspectrophotometrically quantified at 10 or 30 days after selective neurotoxin lesions of either granule cells or CA3 pyramidal cells, and electrolytic lesions of medial septum. Groups with elevated zinc density at 10 days also had significantly higher NA levels at 30 days. Destruction of granule cells eliminated the rise in zinc and prevented the NA increase. The zinc increase may be related to a nerve growth factor-like protein responsible for the initiation of sympathetic sprouting.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Neural transplantation ; Acetylcholine ; Hippocampus ; Spatial memory ; Atropine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The ability of intrahippocampal grafts of fetal septal-diagonal band tissue, rich in developing cholinergic neurons, to ameliorate cognitive impairments induced by bilateral fimbria-fornix transections in rats was examined in three experiments using the Morris water-maze to test different aspects of spatial memory. Experiment 1. Rats with fimbria-fornix lesions received either septal cell suspension grafts or solid septal grafts; normal rats and rats with lesions alone were used as controls. Sixteen weeks after surgery, the rats' spatial learning and memory were tested in the water-maze using a place test, designed to investigate place navigation performance, in which rats learned to escape from the water by swimming to a platform hidden beneath the water's surface. After 5 days of training, the rats were given a spatial probe test in which the platform was removed from the tank to test spatial reference memory. Experiment 2. The same rats used in Exp. 1 were tested in a delayed-match-to-sample, working memory version of the water-maze task. The platform was located in one of two possible locations during each trial, which was composed of 2 swims. If the rat remembered the location of the platform on the 2nd swim of a trial, it should find the platform more quickly on that swim, and thereby demonstrate working memory. Experiment 3. Prior to receiving fimbria-fornix lesions, normal rats were trained in a modification of the water-maze task using alternating cue navigation and place navigation trials (i.e., with visible or non-visible escape platforms). The retention and reacquisition of the place task and the spatial probe test were examined in repeated tests up to 6 months after the lesion and intrahippocampal grafting of septal cell suspensions. The effects of central muscarinic cholinergic receptor blockade with atropine were also tested. Normal rats performed well in both the place and spatial probe tests. In contrast, rats with fimbria-fornix lesions only were unable to acquire or retain spatial information in any test. Instead, these rats adopted a random, nonspatial search strategy, whereby their latencies to find the platform decreased in the place navigation tasks. Sixty to 80% of the rats with septal suspension or solid grafts had recovered place navigation, i.e., the ability to locate the platform site in the tank, in Exp. 1 and 3, and they showed a significantly improved performance in the working memory test in Exp. 2. Atropine abolished the recovered place navigation in the grafted rats, whereas normal rats were impaired to a lesser extent. In contrast, atropine had no effect on the non-spatial strategy adopted by rats with fimbria-fornix lesions only. The results show that: (1) fimbria-fornix lesions disrupt spatial learning and memory in both naive and pretrained rats; (2) with extended training the fimbria-fornix lesioned rats develop an efficient non-spatial strategy, which enables them to reduce their escape latency to levels close to those of intact controls; (3) intrahippocampal septal grafts can restore the ability of the lesioned rats to use spatial cues in the localization of the platform site; and (4) the behavioural recovery produced by grafts is dependent upon an atropine sensitive mechanism.
    Type of Medium: Electronic Resource
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