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

Author:

ALRashdi Barakat M.1,Mohamed Roaya A.2,Mohamed Amal H.2,Samoul Feryal A.2,Mohamed Mazen I.2,Moussa Mohsen M.2,Alrashidi Saad M.3,Dawod Bassel456,Habotta Ola A.7,Abdel Moneim Ahmed E.8ORCID,Ramadan Shimaa S.2

Affiliation:

1. 1Department of Biology, College of Science, Jouf University, Sakaka 72388, Saudi Arabia

2. 2Department of Chemistry, Faculty of Science, Helwan University, Cairo, Egypt

3. 3Consultant Radiation Oncology, Comprehensive Cancer Centre, King Fahad Medical City and College of medicine, Alfaisal University, Riyadh, Saudi Arabia

4. 4McMaster Children’s Hospital, Faculty of Health Sciences, Hamilton, Ontario, Canada

5. 5Department of Biology, College of Science, Jouf University, Sakaka, Al-Jouf, Saudi Arabia

6. 6Department of Zoology, Faculty of Science, Fayoum University, Fayoum, Egypt

7. 7Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt

8. 8Zoology and Entomology Department, Faculty of Science, Helwan University, Cairo, Egypt

Abstract

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.

Funder

Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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