Evidence map›Paper›PMID 37212591›Full record

ArticleJournal of visualized experiments : JoVE2023

A Modified Transcranial Middle Cerebral Artery Occlusion Model to Study Stroke Outcomes in Aged Mice.

Huaxin Sheng, Lihong Dang, Xuan Li, Zhong Yang, Wei Yang

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 4 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

5 authors at 2 institutions in 1 country.

Huaxin ShengMultidisciplinary Brain Protection Program, Department of Anesthesiology, Duke University Medical Center; huaxin.sheng@duke.edu.
Lihong DangMultidisciplinary Brain Protection Program, Department of Anesthesiology, Duke University Medical Center.
Xuan LiMultidisciplinary Brain Protection Program, Department of Anesthesiology, Duke University Medical Center.
Zhong YangMultidisciplinary Brain Protection Program, Department of Anesthesiology, Duke University Medical Center.
Wei YangMultidisciplinary Brain Protection Program, Department of Anesthesiology, Duke University Medical Center; wei.yang@duke.edu.
Duke Medical Center · USDuke University Hospital · US

Funding

The Unfolded Protein Response in Ischemic StrokeR01NS099590 · NINDS · DUKE UNIVERSITY · PI Wei Yang · 2016 to 2026
$3.7M
Immunosuppression after cardiac arrest and resuscitationR01HL157354 · NHLBI · DUKE UNIVERSITY · PI YANG, WEI · 2022 to 2025
$1.6M
Mast cell activation as a determinant of neurologic injury after cardiac arrestR21NS117973 · NINDS · DUKE UNIVERSITY · PI YANG, WEI · 2020 to 2021
$453k
Targeted neuromodulation to enhance recovery of the aged brain after ischemic strokeR21NS127163 · NINDS · DUKE UNIVERSITY · PI YANG, WEI · 2022 to 2022
$443k
NHLBI NIH HHS R01 HL157354NINDS NIH HHS R01 NS099590NINDS NIH HHS R21 NS117973NINDS NIH HHS R21 NS127163
6 · The paper itself

Abstract

In experimental stroke research, middle cerebral artery occlusion (MCAO) with an intraluminal filament is widely used to model ischemic stroke in mice. The filament MCAO model typically exhibits a massive cerebral infarction in C57Bl/6 mice that sometimes includes brain tissue in the territory supplied by the posterior cerebral artery, which is largely due to a high incidence of posterior communicating artery atresia. This phenomenon is considered a major contributor to the high mortality rate observed in C57Bl/6 mice during long-term stroke recovery after filament MCAO. Thus, many chronic stroke studies exploit distal MCAO models. However, these models usually produce infarction only in the cortex area, and consequently, the assessment of post-stroke neurologic deficits could be a challenge. This study has established a modified transcranial MCAO model in which the MCA at the trunk is partially occluded either permanently or transiently via a small cranial window. Since the occlusion location is relatively proximal to the origin of the MCA, this model generates brain damage in both the cortex and striatum. Extensive characterization of this model has demonstrated an excellent long-term survival rate, even in aged mice, as well as readily detectable neurologic deficits. Therefore, the MCAO mouse model described here represents a valuable tool for experimental stroke research.

Indexed as

Ischemic StrokeStrokeAnimalsBrainDisease Models, AnimalInfarction, Middle Cerebral ArteryMiceMice, Inbred C57BLMiddle Cerebral Artery

Identifiers

PMID37212591
PMCPMC10913267
OpenAlexW4372206679

What OpenQuestion holds

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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.