Evidence map›Paper›PMID 22408439›Full record

ArticleInternational journal of molecular sciences2012

Neuroprotective effects of pre-treatment with l-carnitine and acetyl-L-carnitine on ischemic injury in vivo and in vitro.

Rui Zhang, Hong Zhang, Zhongxia Zhang, Tao Wang, Jingya Niu, Dongsheng Cui, Shunjiang Xu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.0field-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

30 citing papers in PubMed, 73 citations in OpenAlex.

  1. Trial
  2. Article
  3. Impact Induces Phagocytic Defect in Reactive Microglia.bioRxiv : the preprint server for biology · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

7 authors at 2 institutions in 1 country.

Rui ZhangCentral Laboratory, The First Hospital of Hebei Medical University, Shijiazhuang 050031, China.
Hong ZhangHandan City Hospital for Infectious Diseases, Handan 056002, China.
Zhongxia ZhangCentral Laboratory, The First Hospital of Hebei Medical University, Shijiazhuang 050031, China.
Tao WangHandan county Hospital, Handan 056002, China.
Jingya NiuCentral Laboratory, The First Hospital of Hebei Medical University, Shijiazhuang 050031, China.
Dongsheng CuiCentral Laboratory, The First Hospital of Hebei Medical University, Shijiazhuang 050031, China.
Shunjiang XuCentral Laboratory, The First Hospital of Hebei Medical University, Shijiazhuang 050031, China.
Hebei Medical University · CNHandan College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The therapeutic effect of stroke is hampered by the lack of neuroprotective drugs against ischemic insults beyond the acute phase. Carnitine plays important roles in mitochondrial metabolism and in modulating the ratio of coenzyme A (CoA)/acyl-CoA. Here, we investigate the neuroprotective effects of l-carnitine (LC) and Acetyl-l-carnitine (ALC) pre-treatment on ischemic insults under the same experimental conditions. We used a transient middle cerebral artery occlusion (MCAO) model to evaluate the protective roles of LC and ALC in acute focal cerebral ischemia in vivo and to understand the possible mechanisms using model of PC12 cell cultures in vitro. Results showed that ALC, but not LC, decreased infarction size in SD rats after MCAO in vivo. However, both LC and ALC pretreatment reduced oxygen-glucose deprivation (OGD)-induced cell injury and decreased OGD-induced cell apoptosis and death in vitro; at the same time, both of them increased the activities of super oxide dismutase (SOD) and ATPase, and decreased the concentration of malondialdehyde (MDA) in vitro. Thus, our findings suggested that LC and ALC pre-treatment are highly effective in the prevention of neuronal cell against ischemic injury in vitro, however, only ALC has the protective effect on neuronal cell injury after ischemia in vivo.

Indexed as

AcetylcarnitineAnimalsApoptosisBrain IschemiaCarnitineInfarction, Middle Cerebral ArteryMaleMalondialdehydeNeuroprotective AgentsOxygenPC12 CellsRatsRats, Sprague-DawleySuperoxide DismutaseAcetylcarnitineCarnitineMalondialdehydeNeuroprotective AgentsOxygenSuperoxide DismutaseAcetyl-l-carnitineischemial-carnitineneuroprotectionoxygen-glucose deprivation

Identifiers

PMID22408439
PMCPMC3292008
OpenAlexW2011606841

What OpenQuestion holds

Textmetadata
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.