» Articles » PMID: 24282792

Gender Difference in Cisplatin-induced Nephrotoxicity in a Rat Model: Greater Intensity of Damage in Male Than Female

Overview
Journal Nephrourol Mon
Publisher Brieflands
Specialty Nephrology
Date 2013 Nov 28
PMID 24282792
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Nephrotoxicity and hepatotoxicity are side effects of Cisplatin (CP) therapy.

Objectives: We investigated the role of gender in CP-induced nephrotoxicity and hepatotoxicity.

Materials And Methods: Low dose of CP (1 mg/kg/day; ip) was administered daily to male and female Wistar rats for 15 consecutive days. Serum creatinine (Cr), blood urea nitrogen (BUN), malondialdehyde (MDA), nitric oxide (NO) metabolite, and magnesium (Mg) levels were determined.

Results: The percentage of weight loss and the serum levels of MDA and nitrite in male and female animals were not statistically different. However, the serum levels of BUN, Cr, Mg, and kidney MDA levels, and kidney weight and damage score were significantly greater in males than in females (P < 0.05).

Conclusions: CP-induced nephrotoxicity is gender related for which the mechanisms should be determined.

Citing Articles

Chemoprotective Mechanism of Sodium Thiosulfate Against Cisplatin-Induced Nephrotoxicity Is via Renal Hydrogen Sulfide, Arginine/cAMP and NO/cGMP Signaling Pathways.

Dugbartey G, Alornyo K, Adams I, Adjei S, Amoah D, Obeng-Kyeremeh R Int J Mol Sci. 2025; 26(1.

PMID: 39796237 PMC: 11720986. DOI: 10.3390/ijms26010384.


Sex and the Kidney Drug-Metabolizing Enzymes and Transporters: Are Preclinical Drug Disposition Data Translatable to Humans?.

Thakur A, Yue G, Ahire D, Mettu V, Al Maghribi A, Ford K Clin Pharmacol Ther. 2024; 116(1):235-246.

PMID: 38711199 PMC: 11218045. DOI: 10.1002/cpt.3277.


Integrated analysis of robust sex-biased gene signatures in human brain.

Wapeesittipan P, Joshi A Biol Sex Differ. 2023; 14(1):36.

PMID: 37221602 PMC: 10207743. DOI: 10.1186/s13293-023-00515-w.


Sex Difference in Cisplatin-Induced Nephrotoxicity: Laboratory and Clinical Findings.

Eshraghi-Jazi F, Nematbakhsh M J Toxicol. 2022; 2022:3507721.

PMID: 36263084 PMC: 9576433. DOI: 10.1155/2022/3507721.


The Prevention of Cisplatin-Induced Nephrotoxicity: A General Consensus Statement of a Group of Oncologist-Hematologists, Adult and Pediatric Nephrologists, Radiation Oncologists, Clinical Pathologists, Clinical Pharmacologists, and Renal....

Ashrafi F, Mortazavi M, Nematbakhsh M Int J Prev Med. 2022; 13:21.

PMID: 35392316 PMC: 8980816. DOI: 10.4103/ijpvm.IJPVM_445_19.


References
1.
Eshraghi-Jazi F, Nematbakhsh M, Nasri H, Talebi A, Haghighi M, Pezeshki Z . The protective role of endogenous nitric oxide donor (L-arginine) in cisplatin-induced nephrotoxicity: Gender related differences in rat model. J Res Med Sci. 2012; 16(11):1389-96. PMC: 3430054. View

2.
Stakisaitis D, Dudeniene G, Jankunas R, Grazeliene G, Didziapetriene J, Pundziene B . Cisplatin increases urinary sodium excretion in rats: gender-related differences. Medicina (Kaunas). 2010; 46(1):45-50. View

3.
Takayama J, Takaoka M, Sugino Y, Yamamoto Y, Ohkita M, Matsumura Y . Sex difference in ischemic acute renal failure in rats: approach by proteomic analysis. Biol Pharm Bull. 2007; 30(10):1905-12. DOI: 10.1248/bpb.30.1905. View

4.
Winston J, Safirstein R . Reduced renal blood flow in early cisplatin-induced acute renal failure in the rat. Am J Physiol. 1985; 249(4 Pt 2):F490-6. DOI: 10.1152/ajprenal.1985.249.4.F490. View

5.
Safari T, Nematbakhsh M, Hilliard L, Evans R, Denton K . Sex differences in the renal vascular response to angiotensin II involves the Mas receptor. Acta Physiol (Oxf). 2012; 206(2):150-6. DOI: 10.1111/j.1748-1716.2012.02468.x. View