Evidence map›Paper›PMID 31165450›Full record

ArticleEnvironmental science and pollution research international2019

Protective effects of zingerone on cisplatin-induced nephrotoxicity in female rats.

Fatih Mehmet Kandemir, Serkan Yildirim, Cuneyt Caglayan, Sefa Kucukler, Gizem Eser

Abstract read
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Article in Environmental science and pollution research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 88 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Fatih Mehmet KandemirDepartment of Biochemistry, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Serkan YildirimDepartment of Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Cuneyt CaglayanDepartment of Biochemistry, Faculty of Veterinary Medicine, Bingol University, 12000, Bingol, Turkey. ccaglayan@bingol.edu.tr.ORCID http://orcid.org/0000-0001-5608-554X
Sefa KucuklerDepartment of Biochemistry, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Gizem EserDepartment of Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Atatürk University · TRBingöl University · TR

Funding

Bingol University BAP-VF.2016.00.001
6 · The paper itself

Abstract

Zingerone (ZO), one of the active components of ginger (Zingiber officinale), is a phenolic alkanone with antioxidant, antiapoptotic, and anti-inflammatory properties. Cisplatin (CP) is a widely used chemotherapeutic drug for solid tumors, but its therapeutic use is limited due to dose-dependent nephrotoxicity. In the present study, we investigated the ameliorative effect of ZO against CP-induced nephrotoxicity. Intraperitoneal administration of single-dose CP (7 mg/kg body weight) on the first day enhanced kidney lipid peroxidation and reduced antioxidant enzyme activities such as catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), and glutathione (GSH). CP increased serum urea and creatinine levels and disrupted histological integrity while causing a decrease aquaporin 1 (AQP1) level in the kidney tissues. CP induced inflammatory responses by elevating the levels of tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6), interleukin-33 (IL-33) and nuclear factor kappa B (NF-κB), and activities of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Moreover, it also caused oxidative DNA damage and activation of apoptotic pathway by increasing of 8-hydroxy-2'-deoxyguanosine (8-OHdG), p53, cysteine aspartate-specific protease-3 (caspase-3), and Bcl-2-associated x protein (bax) while decreasing B cell lymphoma-2 (Bcl-2). However, treatment with ZO at a dose of 25 and 50 mg/kg b.wt. for 7 days significantly decreased oxidative stress, apoptosis, inflammation, and histopathological alterations while increased AQP1 levels in the kidney tissue. The results of the current study suggested that ZO as an effective natural product attenuates CP-induced nephrotoxicity.

Indexed as

AntioxidantsCisplatinGuaiacolKidney8-Hydroxy-2'-DeoxyguanosineAnimalsApoptosisAutophagyBlood Urea NitrogenCatalaseDeoxyguanosineDNA DamageFemaleGlutathioneGlutathione PeroxidaseInflammation8-Hydroxy-2'-DeoxyguanosineAntioxidantsCatalaseCisplatinDeoxyguanosineGlutathioneGlutathione PeroxidaseGuaiacolInterleukin-6NF-kappa BSuperoxide DismutaseTumor Necrosis Factor-alphazingeroneApoptosisCisplatinInflammationNephrotoxicityOxidative stressZingerone

Identifiers

PMID31165450
OpenAlexW2948303250

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.