Evidence map›Paper›PMID 11354828›Full record

ArticleNeurogenetics2001

Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stress.

C A Evans, M S Harbuz, T Ostenfeld, A Norrish, J M Blackwell

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In one paragraph

Article in Neurogenetics, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 39 citations in OpenAlex.

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  13. SLC11 family of H+-coupled metal-ion transporters NRAMP1 and DMT1.Pflugers Archiv : European journal of physiology · 2004
    Review
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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

5 authors at 3 institutions in 1 country.

C A EvansWellcome Trust Centre for Molecular Mechanisms in Disease, Wellcome Trust/MRC Building, Addenbrooke's Hospital, Cambridge, CB2 2XY, UK.
M S Harbuz
T Ostenfeld
A Norrish
J M Blackwell
Wellcome Trust · GBUniversity of Bristol · GBUniversity of Cambridge · GB

Funding

Wellcome Trust 065642
6 · The paper itself

Abstract

The gene Nramp1 encoding the natural resistance-associated macrophage protein (Nramp1) influences susceptibility to intracellular infections and autoimmune diseases, and the humoral response to stress. Nramp1 functions as a proton/divalent cation antiporter in the membranes of late endosomes/lysosomes, regulating cytoplasmic iron levels in macrophages. The Drosophila homologue of Nramp1 is expressed in sensory neurons and macrophages, and influences taste behaviour directly through divalent cation transport. Here we demonstrate that murine Nramp1 is also expressed on neurons as well as microglial cells in the brain and influences the behavioural response to stress, hypothalamus-pituitary-adrenal (HPA) axis activation and mortality following Toxoplasma gondii infection in control and prestressed mice. We hypothesise that, although differences in HPA activation translate into differences in adrenal enlargement and basal circulating corticosterone levels, the primary influence of Nramp1 is at the level of the neuronal response to stress. These results provide new insight into the possible roles of divalent cation transporters of the Nramp gene family in regulating metal ion homeostasis in the brain and its pathological implications.

Indexed as

Cation Transport ProteinsAdrenal GlandsAnimalsAntibody FormationCarrier ProteinsCells, CulturedCorticotropin-Releasing HormoneEmbryo, MammalianEmbryo, NonmammalianKidneyMembrane ProteinsMiceMice, Inbred C57BLMice, Mutant StrainsMicrotubule-Associated ProteinsNatural Resistance-associated Macrophage Protein 1Carrier ProteinsCation Transport ProteinsCorticotropin-Releasing HormoneMembrane ProteinsMicrotubule-Associated ProteinsNatural Resistance-associated Macrophage Protein 1

Identifiers

PMID11354828
PMCPMC2409433
OpenAlexW2055315004

What OpenQuestion holds

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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.