Evidence map›Paper›PMID 30513373›Full record

ArticleNeuroscience2019

Hippocampal Lateralization and Synaptic Plasticity in the Intact Rat: No Left-Right Asymmetry in Electrically Induced CA3-CA1 Long-Term Potentiation.

Stephen J Martin, Kate L Shires, Bruno M da Silva

Open access · hybridAbstract read
In one paragraph

Article in Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 21 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

3 authors at 3 institutions in 1 country.

Stephen J MartinDivision of Systems Medicine, University of Dundee, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK; Centre for Cognitive and Neural Systems (CCNS), University of Edinburgh, 1 George Square, Edinburgh EH8 9JZ, UK. Electronic address: s.martin@dundee.ac.uk.
Kate L ShiresCardiff University Biobank, Cardiff University, Dental Drive, Heath Park, Cardiff CF14 4AX, UK; Centre for Cognitive and Neural Systems (CCNS), University of Edinburgh, 1 George Square, Edinburgh EH8 9JZ, UK.
Bruno M da SilvaCentre for Cognitive and Neural Systems (CCNS), University of Edinburgh, 1 George Square, Edinburgh EH8 9JZ, UK.
Cardiff University · GBUniversity of Dundee · GBUniversity of Edinburgh · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

The hippocampus is not a unitary, homogeneous brain area. Anatomical and functional specialization is evident along the septotemporal axis of the structure, and between the left and right hemispheres. In the mouse brain, a left-right asymmetry has been discovered in the plasticity of CA3-CA1 projections originating in the left versus right hippocampus. Presynaptic afferents originating in the left hemisphere-including both uncrossed Schaffer collaterals, and crossed commissural projections to the contralateral CA1-form small, plastic synapses, whereas afferents originating in right CA3 contact larger, less plastic, synapses. Studies using optogenetic techniques to selectively activate fibers originating from one hemisphere in ex vivo slices have revealed that projections originating from left CA3 exhibit a far greater capacity for long-term potentiation (LTP) of synaptic strength than those originating on the right. However, corresponding data from rats are currently unavailable, leaving open the question of species differences in hippocampal symmetry. In the current study, we reanalyzed data from our previous in vivo LTP work to address this issue. We analyzed plasticity in independent Schaffer collateral and commissural projections to CA1 originating from left and right CA3 in male Lister-hooded rats. However, we found no differences in the magnitude and duration of LTP induced in either crossed or uncrossed pathways following high-frequency tetanization of left versus right CA3. This contrast with previous findings may stem from methodological differences between in vivo electrical and ex vivo optogenetic approaches, but may reflect a genuine species difference in the organization and laterality of the rodent CA3-CA1 system.

Indexed as

Functional LateralityAnimalsElectric StimulationHippocampusLong-Term PotentiationMaleMicroelectrodesRatsSynapsescommissuralhippocampusin vivoLTPSchaffer collateralsynaptic plasticity

Identifiers

PMID30513373
PMCPMC6347473
OpenAlexW2903385029

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.