Evidence map›Paper›PMID 24827566›Full record

ArticleJournal of the American Association for Laboratory Animal Science : JAALAS2014

Enrichment with wood blocks does not affect toxicity assessment in an exploratory toxicology model using Sprague-Dawley rats.

Amy C Ditewig, Natalie A Bratcher, Donna R Davila, Brian D Dayton, Paige Ebert, Philippe Lesuisse, Michael J Liguori, Jill M Wetter, Hyuna Yang, Wayne R Buck

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Association for Laboratory Animal Science : JAALAS, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Effects of Nesting Material on the Toxicologic Assessment of Cyclophosphamide in Crl:CD1(ICR) Mice.Journal of the American Association for Laboratory Animal Science : JAALAS · 2018
    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

10 authors at 3 institutions in 1 country.

Amy C DitewigCellular, Molecular, and Exploratory Toxicology, DSS, AbbVie, North Chicago, Illinois, USA.
Natalie A BratcherOffice of Animal Welfare and Compliance, DSS, AbbVie, North Chicago, Illinois, USA.
Donna R DavilaToxicology, DSS, AbbVie, North Chicago, Illinois, USA.
Brian D Dayton630 East Golf Road, Libertyville, Illinois, USA.
Paige EbertComparative Medicine, DSS, AbbVie, North Chicago, Illinois, USA.
Philippe LesuisseCellular, Molecular, and Exploratory Toxicology, DSS, AbbVie, North Chicago, Illinois, USA.
Michael J LiguoriCellular, Molecular, and Exploratory Toxicology, DSS, AbbVie, North Chicago, Illinois, USA.
Jill M WetterExploratory Kinetics, DSS, AbbVie, North Chicago, Illinois, USA.
Hyuna YangExploratory Statistics, DSS, AbbVie, North Chicago, Illinois, USA.
Wayne R BuckCellular, Molecular, and Exploratory Toxicology, DSS, AbbVie, North Chicago, Illinois, USA. wayne.buck@AbbVie.com.
AbbVie (United States) · USAnimal Welfare Institute · USUnited States Golf Association · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Environmental enrichment in rodents may improve animal well-being but can affect neurologic development, immune system function, and aging. We tested the hypothesis that wood block enrichment affects the interpretation of traditional and transcriptomic endpoints in an exploratory toxicology testing model using a well-characterized reference compound, cyclophosphamide. ANOVA was performed to distinguish effects of wood block enrichment separate from effects of 40 mg/kg cyclophosphamide treatment. Biologically relevant and statistically significant effects of wood block enrichment occurred only for body weight gain. ANOVA demonstrated the expected effects of cyclophosphamide on food consumption, spleen weight, and hematology. According to transcriptomic endpoints, cyclophosphamide induced fewer changes in gene expression in liver than in spleen. Splenic transcriptomic pathways affected by cyclophosphamide included: iron hemostasis; vascular tissue angiotensin system; hepatic stellate cell activation and fibrosis; complement activation; TGFβ-induced hypertrophy and fibrosis; monocytes, macrophages, and atherosclerosis; and platelet activation. Changes in these pathways due to cyclophosphamide treatment were consistent with bone marrow toxicity regardless of enrichment. In a second study, neither enrichment nor type of cage flooring altered body weight or food consumption over a 28-d period after the first week. In conclusion, wood block enrichment did not interfere with a typical exploratory toxicology study; the effects of ingested wood on drug level kinetics may require further consideration.

Indexed as

RatsAdministration, OralAnimalsAnimals, LaboratoryAntineoplastic Agents, AlkylatingBody WeightCyclophosphamideLiverMaleRats, Sprague-DawleyToxicologyWoodAntineoplastic Agents, AlkylatingCyclophosphamide

Identifiers

PMID24827566
PMCPMC4128562
OpenAlexW89558248

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.