Evidence map›Paper›PMID 28273120›Full record

ArticlePloS one2017

Further investigation of phenotypes and confounding factors of progressive ratio performance and feeding behavior in the BACHD rat model of Huntington disease.

Erik Karl Håkan Clemensson, Laura Emily Clemensson, Benedikt Fabry, Stefanie Flunkert, Olaf Riess, Robert Wronski, Huu Phuc Nguyen

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In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Erik Karl Håkan ClemenssonInstitute of Medical Genetics and Applied Genomics, Tuebingen, Tuebingen, Germany.ORCID 0000-0002-5158-6924
Laura Emily ClemenssonInstitute of Medical Genetics and Applied Genomics, Tuebingen, Tuebingen, Germany.
Benedikt FabryQPS Austria, Grambach, Austria.
Stefanie FlunkertQPS Austria, Grambach, Austria.
Olaf RiessInstitute of Medical Genetics and Applied Genomics, Tuebingen, Tuebingen, Germany.
Robert WronskiQPS Austria, Grambach, Austria.
Huu Phuc NguyenInstitute of Medical Genetics and Applied Genomics, Tuebingen, Tuebingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Huntington disease is an inherited neurodegenerative disorder characterized by motor, cognitive, psychiatric and metabolic symptoms. We recently published a study describing that the BACHD rat model of HD shows an obesity phenotype, which might affect their motivation to perform food-based behavioral tests. Further, we argued that using a food restriction protocol based on matching BACHD and wild type rats' food consumption rates might resolve these motivational differences. In the current study, we followed up on these ideas in a longitudinal study of the rats' performance in a progressive ratio test. We also investigated the phenotype of reduced food consumption rate, which is typically seen in food-restricted BACHD rats, in greater detail. In line with our previous study, the BACHD rats were less motivated to perform the progressive ratio test compared to their wild type littermates, although the phenotype was no longer present when the rats' food consumption rates had been matched. However, video analysis of food consumption tests suggested that the reduced consumption rate found in the BACHD rats was not entirely based on differences in hunger, but likely involved motoric impairments. Thus, restriction protocols based on food consumption rates are not appropriate when working with BACHD rats. As an alternative, we suggest that studies where BACHD rats are used should investigate how the readouts of interest are affected by motivational differences, and use appropriate control tests to avoid misleading results. In addition, we show that BACHD rats display distinct behavioral changes in their progressive ratio performance, which might be indicative of striatal dysfunction.

Indexed as

Feeding BehaviorPhenotypeAnalysis of VarianceAnimal FeedAnimalsBehavior, AnimalBiomarkersBody CompositionDisease Models, AnimalDisease ProgressionHuntington DiseaseLeptinMaleRatsBiomarkersLeptin

Identifiers

PMID28273120
PMCPMC5342229

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Registered trials

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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.