Literature DB >> 8851913

Neural grafting of cholinergic neurons in the hippocampal formation.

B J Tarricone1, J R Simon, Y J Li, W C Low.   

Abstract

The cholinergic septohippocampal system plays an important role in spatial learning and memory functions. Transections of the septohippocampal pathway have been shown to result in a near complete loss of cholinergic innervation in the hippocampus and induce severe spatial memory impairments. In this article, we have reviewed the studies which demonstrate the ability of intrahippocampal septal grafts to reinnervate the hippocampal formation and ameliorate spatial learning and memory deficits. Neuroanatomical studies suggest that grafts of cholinergic tissue can innervate the host hippocampal formation in a pattern that mimics that of the normal septohippocampal pathway. This innervation, in turn, is associated with the formation of graft-to-host synaptic connections. Neurochemical studies reveal that intrahippocampal grafts of septal cells can restore choline acetyltransferase activity, acetylcholine synthesis, and high affinity choline uptake in presynaptic terminals of grafted neurons. In addition, these grafts can normalize the upregulation of cholinergic muscarinic receptors seen postsynaptically in the hippocampus following lesions of the septohippocampal pathway. The functional nature of these grafts is also substantiated by electrophysiological recordings which demonstrate stimulus-evoked graft-to-host synaptic transmission as well as the reinstatement of EEG activity typical of septohippocampal connectivity. In addition to graft-to-host connections, behavioral and neurochemical studies also provide evidence for host-to-graft connections that can regulate the activity of grafted cholinergic neurons during the performance of specific behavioral tasks requiring spatial memory function. Together, these studies suggest that grafts of cholinergic neurons from the medial septal nucleus can become anatomically and functionally incorporated into the circuitry of the host hippocampal formation.

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Year:  1996        PMID: 8851913     DOI: 10.1016/0166-4328(95)00144-1

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  4 in total

1.  Fetal hippocampal grafts containing CA3 cells restore host hippocampal glutamate decarboxylase-positive interneuron numbers in a rat model of temporal lobe epilepsy.

Authors:  A K Shetty; D A Turner
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

2.  Exposure of postnatal rats to a static magnetic field of 0.14 T influences functional laterality of the hippocampal high-affinity choline uptake system in adulthood; in vitro test with magnetic nanoparticles.

Authors:  Z Kristofiková; M Cermák; O Benesová; J Klaschka; P Zach
Journal:  Neurochem Res       Date:  2005-02       Impact factor: 3.996

Review 3.  Septohippocampal acetylcholine: involved in but not necessary for learning and memory?

Authors:  Marise B Parent; Mark G Baxter
Journal:  Learn Mem       Date:  2004 Jan-Feb       Impact factor: 2.460

4.  Fructus mume extracts alleviate cognitive impairments in 5XFAD transgenic mice.

Authors:  Jung-Cheol Park; Jinhua Ma; Won Kyung Jeon; Jung-Soo Han
Journal:  BMC Complement Altern Med       Date:  2016-02-06       Impact factor: 3.659

  4 in total

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