Evidence map›Paper›PMID 40358798›Full record

ArticleJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2025

Protective Effect of HMG-CoA Reductase Inhibitor Rosuvastatin on Doxorubicin-Induced Cognitive Impairment, Oxidative Stress and Neuroinflammation: Possible Role of CREB, ERK1/2, and BDNF.

Yesim Yeni, Betul Cicek, Ahmet Hacimuftuoglu, Mustafa Ozkaraca, Burak Batuhan Lacin

Abstract read
In one paragraph

Article in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Neuroprotective Effect of the Combined Extract ofInternational journal of molecular sciences · 2026
    Article
  5. Article
  6. 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

5 authors.

Yesim YeniFaculty of Medicine, Department of Medical Pharmacology, Malatya Turgut Ozal University, Malatya, Turkey. yesim.yeni@ozal.edu.tr.ORCID https://orcid.org/0000-0002-6719-7077
Betul CicekFaculty of Medicine, Department of Physiology, Erzincan Binali Yildirim University, Erzincan, Turkey.ORCID https://orcid.org/0000-0003-1395-1326
Ahmet HacimuftuogluFaculty of Medicine, Department of Medical Pharmacology, Ataturk University, Erzurum, Turkey.ORCID https://orcid.org/0000-0002-9658-3313
Mustafa OzkaracaFaculty of Veterinary Medicine, Department of Pathology, Sivas Cumhuriyet University, Sivas, Turkey.ORCID https://orcid.org/0000-0001-9765-4569
Burak Batuhan LacinFaculty of Veterinary Medicine, Department of Physiology, Ataturk University, Erzurum, Turkey.ORCID https://orcid.org/0000-0002-5701-3684

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During or after chemotherapy, cognitive impairments characterized by forgetfulness, difficulty concentrating, and depressive and anxiety-like symptoms are observed. There is limited research examining the effects of rosuvastatin (RVS), an HMG-CoA reductase inhibitor, in the context of neuroinflammation-related cognitive disruption. Here, we aimed to investigate the neuroprotective potential of RVS against doxorubicin (DOX)-induced cognitive impairments. Experimental groups were planned as control (normal saline, intraperitoneal), DOX (total cumulative dose 10 mg/kg, intraperitoneal), RVS (10 mg/kg, oral, 20 days), and RVS + DOX. Efficacy was monitored by applying a battery of behavioral assessments, as well as biochemical, genetic, histopathological, and immunohistochemical examinations. Results from Morris water maze (MWM), passive avoidance, locomotion activity, and elevated plus maze (EPM) tests showed that DOX administration caused behavioral disorders. Moreover, DOX increased the levels of inducible nitric oxide synthase (iNOS), malondialdehyde (MDA), and tumor necrosis factor-α (TNF-α), while decreasing the levels of interleukin-10 (IL-10), glutathione (GSH), superoxide dismutase, catalase (SOD), endothelial nitric oxide (eNOS), and catalase (CAT). Co-treatment with RSV significantly attenuated DOX-induced behavioral changes and oxidative stress markers. In addition, similar to the immunohistochemical results, we determined that it increased the expression levels of extracellular signal-related kinases 1/2 (ERK1/2), cyclic adenosine monophosphate response element binding protein (CREB), and brain-derived neurotrophic factor (BDNF) and restored the histopathological structure of the brain. Therefore, these results indicated that RSV has a neuroprotective effect against DOX-induced cognitive impairment by reducing neurobehavioral impairments, exerting antioxidant and anti-inflammatory effects, and modulating brain growth factors.

Indexed as

Cognitive DysfunctionDoxorubicinHydroxymethylglutaryl-CoA Reductase InhibitorsNeuroinflammatory DiseasesNeuroprotective AgentsOxidative StressRosuvastatin CalciumAnimalsAntibiotics, AntineoplasticBrain-Derived Neurotrophic FactorCyclic AMP Response Element-Binding ProteinMaleMAP Kinase Signaling SystemRatsRats, WistarAntibiotics, AntineoplasticBdnf protein, ratBrain-Derived Neurotrophic FactorCreb1 protein, ratCyclic AMP Response Element-Binding ProteinDoxorubicinHydroxymethylglutaryl-CoA Reductase InhibitorsNeuroprotective AgentsRosuvastatin CalciumCognitive impairmentDoxorubicinNeuroinflammationNeuroplasticityRosuvastatin

Identifiers

PMID40358798
PMCPMC12075306

What Socratic holds

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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 Socratic graph.