Evidence map›Paper›PMID 41851709›Full record

ArticleBMC complementary medicine and therapies2026

The protective effects of naringin against cisplatin-induced pulmonary toxicity in rats: Insights into the modulation of ER stress and SIRT1/Nrf2 pathway.

Nihal Turkmen Alemdar, Selim Demir, Esin Yulug, Nadire Sevdenur Erdogan, Elif Ayazoglu Demir, Ahmet Mentese, Yuksel Aliyazicioglu

Abstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2026. 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. 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.

Nihal Turkmen AlemdarDepartment of Medical Services and Techniques, Vocational School of Health Services, Recep Tayyip Erdogan University, Rize, Türkiye, 53100, Turkey.
Selim DemirDepartment of Medical Biochemistry, Faculty of Medicine, Karadeniz Technical University, Trabzon, Türkiye, 61080, Turkey. selim.demir@ktu.edu.tr.ORCID http://orcid.org/0000-0002-1863-6280
Esin YulugDepartment of Histology and Embryology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Türkiye, 61080, Turkey.
Nadire Sevdenur ErdoganDepartment of Histology and Embryology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Türkiye, 61080, Turkey.
Elif Ayazoglu DemirDepartment of Chemistry and Chemical Processing Technologies, Macka Vocational School, Karadeniz Technical University, Trabzon, Türkiye, 61750, Turkey.
Ahmet MenteseDepartment of Medical Biochemistry, Faculty of Medicine, Karadeniz Technical University, Trabzon, Türkiye, 61080, Turkey.
Yuksel AliyaziciogluDepartment of Medical Biochemistry, Faculty of Medicine, Karadeniz Technical University, Trabzon, Türkiye, 61080, Turkey.

Funding

Recep Tayyip Erdogan Üniversitesi 02026001026071
6 · The paper itself

Abstract

backgroundCisplatin (CIS) is a chemotherapeutic agent which is frequently utilised in the treatment of ovarian, breast, testicular and lung cancer. Nevertheless, the potential for severe and irreversible toxicity to the lungs restricts its utilisation. Naringin (NRG), a flavanone glycoside found in significant quantities in citrus fruits, has been demonstrated to exert protective effects against oxidative tissue damage. The present study aimed to assess the protective effect of NRG against CIS-induced pulmonary toxicity.

methodsThe administration of NRG (50 and 100 mg/kg) was conducted orally over a period of seven days. CIS (7.5 mg/kg, IP) was administered on day 2 to rats, and lung samples were collected on day 8.

resultsThe CIS application induced lipid peroxidation (LPO), inflammation, and endoplasmic reticulum stress (ERS) in the lung, resulting in the emergence of histopathological findings. However, the administration of NRG was found to be capable of preventing lung injury by suppressing LPO, inflammation and ERS levels in a dose-dependent manner. Furthermore, the suppression of CIS-induced sirtuin1(SIRT1)/nuclear factor-erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) signaling was abolished by NRG supplementation.

conclusionsThe present study has shown, for the first time, that NRG has a potential for protection against lung injury by modulating SIRT1/Nrf2/HO-1 signalling in the context of CIS-induced lung injury.

Indexed as

CisplatinEndoplasmic Reticulum StressFlavanonesLung InjuryAnimalsAntineoplastic AgentsLipid PeroxidationLungMaleNF-E2-Related Factor 2Oxidative StressRatsRats, Sprague-DawleySignal TransductionSirtuin 1Antineoplastic AgentsCisplatinFlavanonesnaringinNfe2l2 protein, ratNF-E2-Related Factor 2Sirt1 protein, ratSirtuin 1CisplatinER stressinflammationlung toxicitynaringinNrf2SIRT1

Identifiers

PMID41851709
PMCPMC13112729

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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.