Evidence map›Paper›PMID 23250994›Full record

ArticleStroke2013

Safety and efficacy evaluation of carnosine, an endogenous neuroprotective agent for ischemic stroke.

Ok-Nam Bae, Kelsey Serfozo, Seung-Hoon Baek, Ki Yong Lee, Anne Dorrance, Wilson Rumbeiha, Scott D Fitzgerald, Muhammad U Farooq, Bharath Naravelta, Archit Bhatt and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Stroke, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Systematic review and stratified meta-analysis of the efficacy of carnosine in animal models of ischemic stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2016
    Pooled it
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  4. Histidine-Containing Dipeptides in Obesity and Cardiometabolic Health: A Systematic Scoping Review.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
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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

11 authors at 3 institutions in 2 countries.

Ok-Nam BaeDepartment of Neurology, Salford Royal Hospital, Stott Lane, Salford, England.
Kelsey Serfozo
Seung-Hoon Baek
Ki Yong Lee
Anne Dorrance
Wilson Rumbeiha
Scott D Fitzgerald
Muhammad U Farooq
Bharath Naravelta
Archit Bhatt
Arshad Majid
Michigan State University · USAjou University · KRHanyang University · KR

Funding

Neuroprotective Evaluation of Asiatic Acid in Preclinical StrokeR21NS064343 · NINDS · MICHIGAN STATE UNIVERSITY · PI MAJID, ARSHAD · 2009 to 2010
$416k
Preclinical efficacy and toxicity evaluation of carnosine in strokeR21NS061067 · NINDS · MICHIGAN STATE UNIVERSITY · PI MAJID, ARSHAD · 2008 to 2009
$366k
NINDS NIH HHS R21 NS061067NINDS NIH HHS R21 NS064343
6 · The paper itself

Abstract

background and purposeAn urgent need exists to develop therapies for stroke that have high efficacy, long therapeutic time windows, and acceptable toxicity. We undertook preclinical investigations of a novel therapeutic approach involving supplementation with carnosine, an endogenous pleiotropic dipeptide.

methodsEfficacy and safety of carnosine treatment was evaluated in rat models of permanent or transient middle cerebral artery occlusion. Mechanistic studies used primary neuronal/astrocytic cultures and ex vivo brain homogenates.

resultsIntravenous treatment with carnosine exhibited robust cerebroprotection in a dose-dependent manner, with long clinically relevant therapeutic time windows of 6 hours and 9 hours in transient and permanent models, respectively. Histological outcomes and functional improvements including motor and sensory deficits were sustained on 14th day poststroke onset. In safety and tolerability assessments, carnosine did not exhibit any evidence of adverse effects or toxicity. Moreover, histological evaluation of organs, complete blood count, coagulation tests, and the serum chemistry did not reveal any abnormalities. In primary neuronal cell cultures and ex vivo brain homogenates, carnosine exhibited robust antiexcitotoxic, antioxidant, and mitochondria protecting activity.

conclusionsIn both permanent and transient ischemic models, carnosine treatment exhibited significant cerebroprotection against histological and functional damage, with wide therapeutic and clinically relevant time windows. Carnosine was well tolerated and exhibited no toxicity. Mechanistic data show that it influences multiple deleterious processes. Taken together, our data suggest that this endogenous pleiotropic dipeptide is a strong candidate for further development as a stroke treatment.

Indexed as

AnimalsBrain IschemiaCarnosineDrug Evaluation, PreclinicalInfusions, IntravenousMaleNeuroprotective AgentsRatsRats, Sprague-DawleyRecovery of FunctionStrokeTreatment OutcomeCarnosineNeuroprotective Agents

Identifiers

PMID23250994
PMCPMC3678096
OpenAlexW2137356761

What OpenQuestion holds

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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.