Evidence map›Paper›PMID 29323183›Full record

ArticleScientific reports2018

Delivery of xenon-containing echogenic liposomes inhibits early brain injury following subarachnoid hemorrhage.

Yi-Feng Miao, Tao Peng, Melanie R Moody, Melvin E Klegerman, Jaroslaw Aronowski, James Grotta, David D McPherson, Hyunggun Kim, Shao-Ling Huang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Nanobiotechnologies for stroke treatment.Nanomedicine (London, England) · 2025
    Review
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  7. Conditioning-based therapeutics for aneurysmal subarachnoid hemorrhage - A critical review.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Review
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  18. Molecular Sensing with Host Systems for HyperpolarizedMolecules (Basel, Switzerland) · 2020
    Review
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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

9 authors at 4 institutions in 2 countries.

Yi-Feng MiaoDivision of Cardiovascular Medicine, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Tao PengDivision of Cardiovascular Medicine, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Melanie R MoodyDivision of Cardiovascular Medicine, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Melvin E KlegermanDivision of Cardiovascular Medicine, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Jaroslaw AronowskiDepartment of Neurology, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
James GrottaStroke Program, Memorial Hermann Hospital, Houston, TX, 77030, USA.
David D McPhersonDivision of Cardiovascular Medicine, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Hyunggun KimDivision of Cardiovascular Medicine, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA. hkim.bme@skku.edu.ORCID http://orcid.org/0000-0001-9797-5872
Shao-Ling HuangDivision of Cardiovascular Medicine, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA. Shaoling.Huang@uth.tmc.edu.
The University of Texas Health Science Center at Houston · USMemorial Hermann · USSungkyunkwan University · KRThe University of Texas Health Science Center · US

Funding

Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
Echogenic Targeted Liposomes:Transfection/Drug DeliveryR01HL074002 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2004 to 2013
$5.3M
Epigenetic Markers and Sustained Cytoprotection for Stroke TreatmentR42NS098918 · NINDS · ZYMO RESEARCH CORPORATION · PI Keith Booher, Shaoling Huang · 2021 to 2026
$4.4M
TARGETED LIPOSOMES FOR ACOUSTIC CARDIOVASCULAR IMAGINGR01HL059586 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 1998 to 2012
$3.2M
Targeted Liposomes for Acoustic Cardiovascular ImagingR56HL059586 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2008 to 2008
$480k
Novel Strategy Development for Neuroprotective Therapeutics Delivery in StrokeR21NS067454 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUANG, SHAOLING · 2010 to 2011
$408k
Epigenetic Markers and Sustained Cytoprotection for Stroke TreatmentR41NS098918 · NINDS · ZYMO RESEARCH CORPORATION · PI BOOHER, KEITH, GUO, WEI · 2017 to 2017
$225k
NCATS NIH HHS UL1 TR000371NHLBI NIH HHS R01 HL059586NHLBI NIH HHS R01 HL074002NHLBI NIH HHS R56 HL059586NINDS NIH HHS R21 NS067454NINDS NIH HHS R41 NS098918NINDS NIH HHS R42 NS098918
6 · The paper itself

Abstract

Xenon (Xe), a noble gas, has promising neuroprotective properties with no proven adverse side-effects. We evaluated neuroprotective effects of Xe delivered by Xe-containing echogenic liposomes (Xe-ELIP) via ultrasound-controlled cerebral drug release on early brain injury following subarachnoid hemorrhage (SAH). The Xe-ELIP structure was evaluated by ultrasound imaging, electron microscopy and gas chromatography-mass spectroscopy. Animals were randomly divided into five groups: Sham, SAH, SAH treated with Xe-ELIP, empty ELIP, or Xe-saturated saline. Treatments were administrated intravenously in combination with ultrasound application over the common carotid artery to trigger Xe release from circulating Xe-ELIP. Hematoma development was graded by SAH scaling and quantitated by a colorimetric method. Neurological evaluation and motor behavioral tests were conducted for three days following SAH injury. Ultrasound imaging and electron microscopy demonstrated that Xe-ELIP have a unique two-compartment structure, which allows a two-stage Xe release profile. Xe-ELIP treatment effectively reduced bleeding, improved general neurological function, and alleviated motor function damage in association with reduced apoptotic neuronal death and decreased mortality. Xe-ELIP alleviated early SAH brain injury by inhibiting neuronal death and bleeding. This novel approach provides a noninvasive strategy of therapeutic gas delivery for SAH treatment.

Indexed as

Administration, IntravenousAnimalsBrain InjuriesDisease Models, AnimalDrug LiberationLiposomesMicroscopy, Electron, TransmissionNeuroprotective AgentsRandom AllocationRatsSubarachnoid HemorrhageUltrasonographyXenonLiposomesNeuroprotective AgentsXenon

Identifiers

PMID29323183
PMCPMC5765033
OpenAlexW2781481194

What OpenQuestion holds

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LicenceCC BY
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.