Evidence map›Paper›PMID 33621218›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2021

Different Responses to Identical Trauma Between BALB/C and C57BL/6 Mice.

Xiuying Chen, Chang Cheng, Wenchao Cheng, Yuhan Wang, Xuzheng Zuo, Weiju Tang, Zhanyang Yu, Zhihuan Yang, Zhengguo Wang, Peifang Zhu and 1 more

Open access · greenAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 86% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 7 institutions in 2 countries.

Xiuying ChenDepartment of Neurology, Second Affiliated Hospital of Army Medical University, Chongqing, China (mainland).
Chang ChengDepartment of Neurology, Second Affiliated Hospital of Army Medical University, Chongqing, China (mainland).
Wenchao ChengDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China (mainland).
Yuhan WangDepartment of Neurology, Second Affiliated Hospital of Army Medical University, Chongqing, China (mainland).
Xuzheng ZuoDepartment of Neurology, Second Affiliated Hospital of Army Medical University, Chongqing, China (mainland).
Weiju TangDepartment of Neurology, Second Affiliated Hospital of Army Medical University, Chongqing, China (mainland).
Zhanyang YuNeuroprotection Research Laboratory, Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Zhihuan YangDepartment 4, Institute of Surgery Research, Daping Hospital, Army Medical University, Chongqing, China (mainland).
Zhengguo WangDepartment 4, Institute of Surgery Research, Daping Hospital, Army Medical University, Chongqing, China (mainland).
Peifang ZhuDepartment 4, Institute of Surgery Research, Daping Hospital, Army Medical University, Chongqing, China (mainland).
Wen HuangDepartment of Neurology, Second Affiliated Hospital of Army Medical University, Chongqing, China (mainland).
Army Medical University · CNChongqing Medical University · CNDaping Hospital · CNSecond Affiliated Hospital of Chongqing Medical University · CNDalian Medical University · CNFirst Affiliated Hospital of Zhengzhou University · CNHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Different responses to identical trauma may be related to the genetic background of individuals, but the molecular mechanism is unclear. In this study we investigated the heterogeneity of trauma in mice and the potential biological explanations for the differences. MATERIAL AND METHODS Compared with other organs, the pathological response of the lung after injury is the earliest and most serious. We used C57BL/6 and BALB/C mice to explore the genetic background of different responses to trauma in the lung. We measured mortality rate, pulmonary microvascular permeability, and Cxcl15 gene expression in BALB/C and C57BL/6 mice before and after blast-wave injury. Microvascular permeability was measured using a fluorescent tracer, and Cxcl15 gene expression level and expression distribution were measured using fluorogenic probe quantitative polymerase chain reaction and northern blot. RESULTS C57BL/6 mice showed lower mortality rates and pulmonary microvascular permeability than BALB/C mice after blast-wave injury; there was no significant difference in the permeability before blast-wave injury. The Cxcl15 gene was expressed specifically in the lung tissue of mice. The level of Cxcl15 expression in BALB/C mice was higher than in C57BL/6 mice before and after injury, and the variation trend of Cxcl15 expression level after injury was significantly different between BALB/C and C57BL/6 mice. CONCLUSIONS Our results indicated that BALB/C and C57BL/6 mice had significant heterogeneity in posttraumatic response in terms of mortality and degree of lung damage. The differences in genetic factors such as Cxcl15 may have played a role in this heterogeneity.

Indexed as

AnimalsBlast InjuriesCapillary PermeabilityChemokines, CXCGene ExpressionLungLung InjuryMaleMiceMice, Inbred BALB CMice, Inbred C57BLWounds and InjuriesChemokines, CXCCxcl15 protein, mouse

Identifiers

PMID33621218
PMCPMC7911832
OpenAlexW3132987593

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.