Evidence map›Paper›PMID 24828655›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Activation of neurotensin receptor 1 facilitates neuronal excitability and spatial learning and memory in the entorhinal cortex: beneficial actions in an Alzheimer's disease model.

Zhaoyang Xiao, Nicholas I Cilz, Lalitha Kurada, Binqi Hu, Chuanxiu Yang, Etsuko Wada, Colin K Combs, James E Porter, Florian Lesage, Saobo Lei

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 63 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Zhaoyang XiaoDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203.
Nicholas I CilzDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203.
Lalitha KuradaDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203.
Binqi HuDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203.
Chuanxiu YangDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203.
Etsuko WadaDepartment of Degenerative Neurological Diseases, National Institute of Neuroscience, Tokyo, Japan, and.
Colin K CombsDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203.
James E PorterDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203.
Florian LesageInstitut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, and Université de Nice Sophia-Antipolis, Sophia-Antipolis, 06560 Valbonne, France.
Saobo LeiDepartment of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota 58203, saobo.lei@med.und.edu.
University of North Dakota · USCentre National de la Recherche Scientifique · FRNational Center of Neurology and Psychiatry · JP

Funding

Roles and mechanisms of neurotensin in learning and memoryR01MH082881 · NIMH · UNIVERSITY OF NORTH DAKOTA · PI LEI, SAOBO · 2008 to 2015
$2.5M
NIMH NIH HHS MH082881NIMH NIH HHS R01 MH082881
6 · The paper itself

Abstract

Neurotensin (NT) is a tridecapeptide distributed in the CNS, including the entorhinal cortex (EC), a structure that is crucial for learning and memory and undergoes the earliest pathological alterations in Alzheimer's disease (AD). Whereas NT has been implicated in modulating cognition, the cellular and molecular mechanisms by which NT modifies cognitive processes and the potential therapeutic roles of NT in AD have not been determined. Here we examined the effects of NT on neuronal excitability and spatial learning in the EC, which expresses high density of NT receptors. Brief application of NT induced persistent increases in action potential firing frequency, which could last for at least 1 h. NT-induced facilitation of neuronal excitability was mediated by downregulation of TREK-2 K(+) channels and required the functions of NTS1, phospholipase C, and protein kinase C. Microinjection of NT or NTS1 agonist, PD149163, into the EC increased spatial learning as assessed by the Barnes Maze Test. Activation of NTS1 receptors also induced persistent increases in action potential firing frequency and significantly improved the memory status in APP/PS1 mice, an animal model of AD. Our study identifies a cellular substrate underlying learning and memory and suggests that NTS1 agonists may exert beneficial actions in an animal model of AD.

Indexed as

Action PotentialsAlzheimer DiseaseAnimalsDisease Models, AnimalEntorhinal CortexMaze LearningMiceNeuronsNeurotensinReceptors, NeurotensinNeurotensinneurotensin type 1 receptorReceptors, Neurotensinglutamateion channelmemorypeptidesynapsesynaptic transmission

Identifiers

PMID24828655
PMCPMC4019809
OpenAlexW2128811302

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.