Evidence map›Paper›PMID 38813032›Full record

ArticleTurkish journal of medical sciences2023

Evaluation of syringin's neuroprotective effect in a model of neonatal hypoxic-ischemic brain injury.

Ezgi Yangın Ergon, Aslı Çelik, Gülden Diniz, Rüya Çolak, Senem Alkan Özdemir, Şebnem Çalkavur, Osman Yilmaz

Abstract read
In one paragraph

Article in Turkish journal of medical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Syringin (Sinapyl Alcohol 4-International journal of molecular sciences · 2025
    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.

Ezgi Yangın ErgonNeonatal Intensive Care Unit, Pediatric Division, Dr Behçet Uz Children's Education and Research Hospital, İzmir, Turkiye.ORCID https://orcid.org/0000-0003-0836-7379
Aslı ÇelikDepartment of Laboratory Animal Science, Faculty of Health Sciences, Dokuz Eylül University, İzmir, Turkiye.ORCID https://orcid.org/0000-0002-2888-6080
Gülden DinizDepartment of Pathology, Medical Faculty, İzmir Democracy University, İzmir, Turkiye.ORCID https://orcid.org/0000-0003-1512-7584
Rüya ÇolakNeonatal Intensive Care Unit, Pediatric Division, Medikal Park Florya Hospital, Aydın University Medical Faculty, İstanbul, Turkiye.ORCID https://orcid.org/0000-0002-8732-7932
Senem Alkan ÖzdemirNeonatal Intensive Care Unit, Pediatric Division, Dr Behçet Uz Children's Education and Research Hospital, İzmir, Turkiye.ORCID https://orcid.org/0000-0003-0474-7120
Şebnem ÇalkavurNeonatal Intensive Care Unit, Pediatric Division, Dr Behçet Uz Children's Education and Research Hospital, İzmir, Turkiye.ORCID https://orcid.org/0000-0002-3820-2690
Osman YilmazDepartment of Laboratory Animal Science, Faculty of Health Sciences, Dokuz Eylül University, İzmir, Turkiye.ORCID https://orcid.org/0000-0001-7817-7576

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: A significant cause of mortality and morbidity in the neonatal era is hypoxic-ischemic encephalopathy (HIE). This study examined the histopathological analysis and neuroprotective impact of syringin (SYR) in an experimental HIE rat model. Material and methods: On the 7th postnatal day, 24 Wistar albino rats were evaluated in 3 groups using the HIE model under gas anesthesia. In the experiment, Group A received 10 mg/kg SYR plus dimethyl sulfoxide (DMSO), Group B received DMSO only, and Group C served as a sham group. Immunohistochemical techniques were used to assess apoptotic cell measurement and proinflammatory cytokines (TNF-α and IL-1β primary antibodies). Results: Rats suffering from hypoxic-ischemic brain damage had their apoptosis assessed. The SYR and sham groups had statistically fewer cells undergoing apoptosis (p < 0.001). There was no difference between the groups in terms of IL-1β and TNF-α during immunohistochemical staining. Neuronal degeneration was significantly lower in the histological evaluation of the hippocampus in the SYR group (p = 0.01). A statistically significant difference (p = 0.01) was observed between the SYR and the control groups regarding pericellular and perivascular edema. Conclusion: SYR reduced apoptosis, perivascular and pericellular edema, and neuronal degeneration in rat cerebral tissue. These results raise the possibility that SYR may have a neuroprotective effect on the harm brought on by HIE. This is the first investigation of SYR's function within the HIE paradigm.

Indexed as

Animals, NewbornDisease Models, AnimalHypoxia-Ischemia, BrainNeuroprotective AgentsRats, WistarAnimalsApoptosisGlucosidesInterleukin-1betaPhenylpropionatesRatsGlucosidesInterleukin-1betaNeuroprotective AgentsPhenylpropionatessyringinantiinflammatoryapoptosisbrain injuryHypoxic-ischemicsyringin

Identifiers

PMID38813032
PMCPMC10763795

What OpenQuestion holds

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Registered trials

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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.