Evidence map›Paper›PMID 35767737›Full record

ArticleBlood advances2022

Development of a carotid artery thrombolysis stroke model in mice.

Jessica A A Maclean, Amelia J Tomkins, Sharelle A Sturgeon, Benjamin R Hofma, Imala Alwis, Andre L Samson, Simone M Schoenwaelder, Shaun P Jackson

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Animal stroke models and outcome evaluation: A review.Animal models and experimental medicine · 2026
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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

8 authors at 3 institutions in 2 countries.

Jessica A A MacleanHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0002-7872-9673
Amelia J TomkinsHeart Research Institute, Newtown, NSW, Australia.
Sharelle A SturgeonHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0002-1871-8972
Benjamin R HofmaHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0002-0432-3136
Imala AlwisHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0002-5459-9093
Andre L SamsonHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0002-0637-2716
Simone M SchoenwaelderHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0003-0465-5840
Shaun P JacksonHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0002-4750-1991
The University of Sydney · AUScripps Research Institute · USThe Heart Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recanalization with restored cerebral perfusion is the primary goal of thrombolytic therapy in acute ischemic stroke. The identification of adjunctive therapies that can be safely used to enhance thrombolysis in stroke remains an elusive goal. We report here the development of a mouse in situ carotid artery thrombolysis (iCAT) stroke model involving graded cerebral ischemia to induce unihemispheric infarction after thrombotic occlusion of the common carotid artery (CCA). Electrolytic-induced thrombotic occlusion of the left CCA enabled real-time assessment of recanalization and rethrombosis events after thrombolysis with recombinant tissue-type plasminogen activator (rtPA). Concurrent transient stenosis of the right CCA induced unihemispheric hypoperfusion and infarction in the left middle cerebral artery territory. Real-time assessment of thrombolysis revealed recanalization rates <30% in rtPA-treated animals with high rates of rethrombosis. Addition of the direct thrombin inhibitor argatroban increased recanalization rates to 50% and reduced rethrombosis. Paradoxically, this was associated with increased cerebral ischemia and stroke-related mortality (25%-42%). Serial analysis of carotid and cerebral blood flow showed that coadministration of argatroban with rtPA resulted in a marked increase in carotid artery embolization, leading to distal obstruction of the middle cerebral artery. Real-time imaging of carotid thrombi revealed that adjunctive anticoagulation destabilized platelet-rich thrombi at the vessel wall, leading to dislodgement of large platelet emboli. These studies confirm the benefits of anticoagulants in enhancing thrombolysis and large artery recanalization; however, at high levels of anticoagulation (∼3-fold prolongation of activated partial thromboplastin time), this effect is offset by increased incidence of carotid artery embolization and distal middle cerebral artery occlusion. The iCAT stroke model should provide important new insight into the effects of adjunctive antithrombotic agents on real-time thrombus dynamics during thrombolysis and their correlation with stroke outcomes.

Indexed as

Brain IschemiaIschemic StrokeStrokeThromboembolismAnimalsAnticoagulantsAntithrombinsArginineCarotid Artery, CommonFibrinolytic AgentsInfarction, Middle Cerebral ArteryMicePipecolic AcidsSulfonamidesThrombolytic TherapyTissue Plasminogen ActivatorAnticoagulantsAntithrombinsargatrobanArginineFibrinolytic AgentsPipecolic AcidsSulfonamidesTissue Plasminogen Activator

Identifiers

PMID35767737
PMCPMC9631707
OpenAlexW4283753139

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.