Evidence map›Paper›PMID 30460866›Full record

ArticlePharmaceutical biology2018

Resveratrol mitigates the oxidative stress mediated by hypoxic-ischemic brain injury in neonatal rats via Nrf2/HO-1 pathway.

Yan Gao, Rongrong Fu, Jue Wang, Xue Yang, Lulu Wen, Juan Feng

Abstract read
In one paragraph

Article in Pharmaceutical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Modulating Role of Resveratrol in Metabolic and Inflammatory Dysregulation Caused by Surgical and Psychoemotional Stress in Rats.Pathophysiology : the official journal of the International Society for Pathophysiology · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Pretreatment with oleuropein protects the neonatal brain from hypoxia-ischemia by inhibiting apoptosis and neuroinflammation.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  18. Resveratrol Effects on Male Infertility.Galen medical journal · 2024
    Review
  19. Review
  20. Review
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

6 authors.

Yan Gaoa Department of Neurology , Shengjing Hospital Affiliated Hospital of China Medical University , Shenyang, Liaoning , China.
Rongrong Fua Department of Neurology , Shengjing Hospital Affiliated Hospital of China Medical University , Shenyang, Liaoning , China.
Jue Wanga Department of Neurology , Shengjing Hospital Affiliated Hospital of China Medical University , Shenyang, Liaoning , China.
Xue Yanga Department of Neurology , Shengjing Hospital Affiliated Hospital of China Medical University , Shenyang, Liaoning , China.
Lulu Wena Department of Neurology , Shengjing Hospital Affiliated Hospital of China Medical University , Shenyang, Liaoning , China.
Juan Fenga Department of Neurology , Shengjing Hospital Affiliated Hospital of China Medical University , Shenyang, Liaoning , China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextHypoxic-ischemic encephalopathy (HIE) has a high morbidity and mortality rate. Resveratrol possesses numerous biological properties including antioxidant, anti-inflammatory and neuroprotective activities.

objectiveThe current experiment investigates the neuroprotective efficacy of resveratrol (RESV) against HIE by modulating Nrf2/HO-1 pathway in neonatal rats. MATERIALS AND

methodsSeven-day-old pups (n = 48) were divided into four groups. Group-I rats receiving 2% DMSO saline (sham), group-II rats underwent unilateral carotid artery ligation and hypoxia (92% N

resultsPre-treatment with RESV (20 or 40) markedly reduced (p < 0.01) the cerebral oedema (86.23-71.26 or 65.24%), infarct area (33.85-19.81 or 14.30%), lipid peroxidation products, inflammatory markers [IL-1β 186-110 or 82; IL-6 255-146 or 103; TNF-α 310-204 or 137; NF-κB 205-115 or 91) p65 subunit] and significantly restored (p < 0.01) the antioxidative status by enhancing the activities of glutathione peroxidase (GPx) 5.22-6.49 or 7.78; catalase (CAT) 51-55 or 59, superoxide dismutase (SOD) 2.5-3.05 or 3.25; through marked upregulation (p < 0.01) of heme oxygenase 1 (HO-1) 0.65-0.69 or 0.73; and nuclear factor erythroid 2 related factor 2 (Nrf2) 0.73-0.86 or 0.91. DISCUSSION AND

conclusionsRESV displays its neurotherapeutic potential via upregulating the protein expression of Nrf2 and HO-1 signalling pathway and thereby attenuates oxidative stress and inflammatory response in HI-induced neonatal rats.

Indexed as

AnimalsAntioxidantsBrain EdemaCerebral CortexCytokinesHeme Oxygenase-1Hypoxia-Ischemia, BrainNeuroprotective AgentsNF-E2-Related Factor 2Oxidative StressRatsRats, Sprague-DawleyResveratrolAntioxidantsCytokinesHeme Oxygenase-1Neuroprotective AgentsNfe2l2 protein, ratNF-E2-Related Factor 2Resveratrolinfarct areainflammatory markersLipid peroxidationneurotherapeuticoedema

Identifiers

PMID30460866
PMCPMC6249550

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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.