L-carnitine suppresses cisplatin-induced renal injury in rats: impact on cytoskeleton proteins expression

Author:

Ebrahim Osama Fouad Ahmed1,Nafea Ola Elsayed23ORCID,Samy Walaa4,Shawky Lamiaa Mohamed5

Affiliation:

1. Department of Anatomy, Faculty of Medicine, Benha University, Benha 13518, Egypt

2. Department of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Zagazig University, Zagazig 44519, Egypt

3. Department of Clinical Pharmacy, Collage of Pharmacy, Taif University, Taif 11099, Saudi Arabia

4. Department of Medical Biochemistry, Faculty of Medicine, Zagazig University, Zagazig 44519, Egypt

5. Department of Histology and Cell Biology, Faculty of Medicine, Benha University, Benha 13518, Egypt

Abstract

Abstract We designed this work to examine the curative role of L-carnitine (LCAR) in a rat model of cisplatin (CDDP)-induced kidney injury. We induced kidney injury in rats by a single intraperitoneal injection of 5 mg/kg of CDDP. Fifteen days post injection, rats were orally supplemented with 354 mg/kg of LCAR for another 15 days. Kidney tissues were subjected to histo-biochemical analysis along with mRNA gene expression quantification for cytoskeleton proteins encoding genes (vimentin, nestin, and connexin 43) by real-time reverse transcription polymerase chain reaction. LCAR reversed CDDP-induced renal structural and functional impairments. LCAR significantly declined serum urea and creatinine concentrations, restored oxidant/antioxidant balance, reversed inflammation, and antagonized caspase 3-mediated apoptotic cell death in renal tissues. Moreover, LCAR effectively down-regulated cytoskeleton proteins mRNA levels, reflecting amelioration of CDDP-provoked podocyte injury. We concluded that LCAR has a favorable therapeutic utility against CDDP-induced kidney injury.

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Toxicology

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