Evidence map›Paper›PMID 37902021›Full record

ArticleBioscience reports2023

Therapeutic activity of green synthesized selenium nanoparticles from turmeric against cisplatin-induced oxido-inflammatory stress and cell death in mice kidney.

Barakat M ALRashdi, Roaya A Mohamed, Amal H Mohamed, Feryal A Samoul, Mazen I Mohamed, Mohsen M Moussa, Saad M Alrashidi, Bassel Dawod, Ola A Habotta, Ahmed E Abdel Moneim and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 3 countries.

Barakat M ALRashdiDepartment of Biology, College of Science, Jouf University, Sakaka 72388, Saudi Arabia.
Roaya A MohamedDepartment of Chemistry, Faculty of Science, Helwan University, Cairo, Egypt.
Amal H MohamedDepartment of Chemistry, Faculty of Science, Helwan University, Cairo, Egypt.
Feryal A SamoulDepartment of Chemistry, Faculty of Science, Helwan University, Cairo, Egypt.
Mazen I MohamedDepartment of Chemistry, Faculty of Science, Helwan University, Cairo, Egypt.
Mohsen M MoussaDepartment of Chemistry, Faculty of Science, Helwan University, Cairo, Egypt.
Saad M AlrashidiConsultant Radiation Oncology, Comprehensive Cancer Centre, King Fahad Medical City and College of medicine, Alfaisal University, Riyadh, Saudi Arabia.
Bassel DawodMcMaster Children's Hospital, Faculty of Health Sciences, Hamilton, Ontario, Canada.
Ola A HabottaDepartment of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
Ahmed E Abdel MoneimZoology and Entomology Department, Faculty of Science, Helwan University, Cairo, Egypt.ORCID 0000-0002-2654-2591
Shimaa S RamadanDepartment of Chemistry, Faculty of Science, Helwan University, Cairo, Egypt.
Helwan University · EGJouf University · SAAlfaisal University · SAMansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cisplatin (CDDP) is a commonly prescribed chemotherapeutic agent; however, its associated nephrotoxicity limits its clinical efficacy and sometimes requires discontinuation of its use. The existing study was designed to explore the reno-therapeutic efficacy of turmeric (Tur) alone or conjugated with selenium nanoparticles (Tur-SeNPs) against CDDP-mediated renal impairment in mice and the mechanisms underlying this effect. Mice were orally treated with Tur extract (200 mg/kg) or Tur-SeNPs (0.5 mg/kg) for 7 days after administration of a single dose of CDDP (5 mg/kg, i.p.). N-acetyl cysteine NAC (100 mg/kg) was used as a standard antioxidant compound. The results revealed that Tur-SeNPs counteracted CDDP-mediated serious renal effects in treated mice. Compared with the controls, Tur or Tur-SeNPs therapy remarkably decreased the kidney index along with the serum levels of urea, creatinine, Kim-1, and NGAL of the CDDP-injected mice. Furthermore, Tur-SeNPs ameliorated the renal oxidant status of CDDP group demonstrated by decreased MDA and NO levels along with elevated levels of SOD, CAT, GPx, GR, GSH, and gene expression levels of HO-1. Noteworthy, lessening of renal inflammation was exerted by Tur-SeNPs via lessening of IL-6 and TNF-α besides down-regulation of NF-κB gene expression in mouse kidneys. Tur-SeNPs treatment also restored the renal histological features attained by CDDP challenge and hindered renal apoptosis through decreasing the Bax levels and increasing Bcl-2 levels. Altogether, these outcomes suggest that the administration of Tur conjugated with SeNPs is effective neoadjuvant chemotherapy to guard against the renal adverse effects that are associated with CDDP therapy.

Indexed as

CisplatinSeleniumAnimalsApoptosisCurcumaKidneyMiceOxidative StressCisplatinSeleniumcisplatininflammationnephrotoxicityoxidative stressselenium nanoparticlesturmeric extract

Identifiers

PMID37902021
PMCPMC10643052
OpenAlexW4388014422

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.