Evidence map›Paper›PMID 32859790›Full record

ArticleNeural regeneration research2021

Neuroprotection by cattle encephalon glycoside and ignotin beyond the time window of thrombolysis in ischemic stroke.

Jun Zhong, Rong-Wei Li, Ju Wang, Ying Wang, Hong-Fei Ge, Ji-Shu Xian, Hua Feng, Liang Tan

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Neural regeneration research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Jun ZhongDepartment of Neurosurgery, Southwest Hospital, The Third Military Medical University (Army Medical University), Chongqing, China.
Rong-Wei LiDepartment of Neurosurgery, Southwest Hospital, The Third Military Medical University (Army Medical University), Chongqing; Department of Neurosurgery, Hanzhong Central Hospital, Hanzhong, Shaanxi Province, China.
Ju WangDepartment of Neurosurgery, Southwest Hospital, The Third Military Medical University (Army Medical University), Chongqing, China.
Ying WangDepartment of Oncology, Hanzhong Central Hospital, Hanzhong, Shaanxi Province, China.
Hong-Fei GeDepartment of Neurosurgery, Southwest Hospital, The Third Military Medical University (Army Medical University), Chongqing, China.
Ji-Shu XianDepartment of Neurosurgery, Southwest Hospital, The Third Military Medical University (Army Medical University), Chongqing, China.
Hua FengDepartment of Neurosurgery, Southwest Hospital, The Third Military Medical University (Army Medical University), Chongqing, China.
Liang TanDepartment of Neurosurgery, Southwest Hospital, The Third Military Medical University (Army Medical University); State Key Laboratory of Power Transmission Equipment and System Security and New Technology, School of Electrical Engineering, Chongqing University, Chongqing, China.
Army Medical University · CNSouthwest Hospital · CNChongqing University · CNHanzhong Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cattle encephalon glycoside and ignotin (CEGI) injection is known as a multi-target neuroprotective drug that contains numerous liposoluble molecules, such as polypeptides, monosialotetrahexosyl ganglioside (GM-1), free amino acids, hypoxanthine and carnosine. CEGI has been approved by the Chinese State Food and Drug Administration and widely used in the treatments of various diseases, such as stroke and Alzheimer's disease. However, the neuroprotective effects of CEGI beyond the time window of thrombolysis (within 4.5 hours) on acute ischemic stroke remain unclear. This study constructed a rat middle cerebral artery occlusion model by suture-occluded method to simulate ischemic stroke. The first daily dose was intraperitoneally injected at 8 hours post-surgery and the CEGI treatments continued for 14 days. Results of the modified five-point Bederson scale, beam balance test and rotameric test showed the neurological function of ischemic stroke rats treated with 4 mL/kg/d CEGI improved significantly, but the mortality within 14 days did not change significantly. Brain MRI and 2,3,5-triphenyltetrazolium chloride staining confirmed that the infarct size in the 4 mL/kg/d CEGI-treated rats was significantly reduced compared with ischemic insult only. The results of transmission electron microscopy and double immunofluorescence staining showed that the hippocampal neuronal necrosis in the ischemic penumbra decreased whereas the immunopositivity of new neuronal-specific protein doublecortin and the percentage of Ki67/doublecortin positive cells increased in CEGI-treated rats compared with untreated rats. Our results suggest that CEGI has an effective neuroprotective effect on ischemic stroke when administered after the time window of thrombolysis. The study was approved by the Animal Ethics Committee of The Third Military Medical University, China.

Indexed as

apoptosisbraincattle encephalon glycoside and ignotincentral nervous systemneurological functionplasticityratregenerationstroke

Identifiers

PMID32859790
PMCPMC7896241
OpenAlexW3080581278

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.