Evidence map›Paper›PMID 27233617›Full record

ArticleNeuroscience2016

Comparable reduction in Zif268 levels and cytochrome oxidase activity in the retrosplenial cortex following mammillothalamic tract lesions.

Aura Frizzati, Michal M Milczarek, Frank Sengpiel, Kerrie L Thomas, Christopher M Dillingham, Seralynne D Vann

Open access · hybridAbstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Time to put the mammillothalamic pathway into context.Neuroscience and biobehavioral reviews · 2021
    Review
  4. Anterior thalamic nuclei neurons sustain memory.Current research in neurobiology · 2021
    Article
  5. Article
  6. The Cognitive Thalamus as a Gateway to Mental Representations.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Review
  7. Article
  8. Article
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

6 authors at 1 institution in 2 countries.

Aura FrizzatiSchool of Psychology, Cardiff University, Tower Building, Park Place, Cardiff CF10 3AT, UK; School of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.
Michal M MilczarekSchool of Psychology, Cardiff University, Tower Building, Park Place, Cardiff CF10 3AT, UK; School of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.
Frank SengpielSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.
Kerrie L ThomasSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.
Christopher M DillinghamSchool of Psychology, Cardiff University, Tower Building, Park Place, Cardiff CF10 3AT, UK; Institute of Neuroscience, Trinity College Dublin, Lloyd Building, College Green, Dublin 2, Ireland.
Seralynne D VannSchool of Psychology, Cardiff University, Tower Building, Park Place, Cardiff CF10 3AT, UK. Electronic address: vannsd@cardiff.ac.uk.
Cardiff University · GB

Funding

Wellcome TrustWellcome Trust WT090954AIAWellcome Trust WT096516/B/11/AWellcome Trust WT102409/Z/13/Z
6 · The paper itself

Abstract

Damage to the mammillothalamic tract (MTT) produces memory impairments in both humans and rats, yet it is still not clear why this diencephalic pathway is vital for memory. One suggestion is that it is an important route for midbrain inputs to reach a wider cortical and subcortical network that supports memory. Consistent with this idea, MTT lesions produce widespread hypoactivity in distal brain regions as measured by the immediate-early gene, c-fos. To determine whether these findings were selective to c-fos or reflected more general changes in neuronal function, we assessed the effects of MTT lesions on the expression of the immediate-early gene protein, Zif268 and the metabolic marker, cytochrome oxidase, in the retrosplenial cortex and hippocampus. The lesions decreased levels of both activity markers in the superficial and deep layers of the retrosplenial cortex in both its granular and dysgranular subregions. In contrast, no significant changes were observed in the hippocampus, despite the MTT-lesioned animals showing marked impairments on T-maze alternation. These findings are consistent with MTT lesions providing important, indirect inputs for normal retrosplenial cortex functioning. These distal functional changes may contribute to the memory impairments observed after MTT lesions.

Indexed as

Analysis of VarianceAnimalsCell CountCerebral CortexCohort StudiesDisease Models, AnimalEarly Growth Response Protein 1Electric StimulationElectron Transport Complex IVHippocampusImmunohistochemistryMammillary BodiesMaze LearningMemory DisordersNeural PathwaysRatsEarly Growth Response Protein 1Egr1 protein, ratElectron Transport Complex IVanterior thalamic nucleidiencephalic amnesiahippocampusimmediate-early genemammillary bodiesmemory

Identifiers

PMID27233617
PMCPMC4936792
OpenAlexW2401016096

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.