Protective Effect of Neutral Electrolyzed Saline on Gentamicin-Induced Nephrotoxicity: Evaluation of Histopathologic Parameters in a Murine Model

Author:

Aurelien-Cabezas Nomely S.1,Paz-Michel Brenda A.12,Jacinto-Cortes Ivan3,Delgado-Enciso Osiris G.13,Montes-Galindo Daniel A.4,Cabrera-Licona Ariana2,Zaizar-Fregoso Sergio A.12ORCID,Paz-Garcia Juan5,Ceja-Espiritu Gabriel1,Melnikov Valery1,Guzman-Esquivel Jose6,Rodriguez-Sanchez Iram P.7ORCID,Martinez-Fierro Margarita L.8ORCID,Delgado-Enciso Ivan12ORCID

Affiliation:

1. School of Medicine, University of Colima, Colima 28040, Mexico

2. Department of Research, Esteripharma SA de CV, Atlacomulco 50450, Mexico

3. Cancerology State Institute, Colima State Health Services, Colima 28085, Mexico

4. School of Chemical Sciences, University of Colima, Coquimatlan 28400, Mexico

5. Union Hospital Center, Villa de Álvarez, Colima 28970, Mexico

6. Clinical Epidemiology Research Unit, Mexican Institute of Social Security Institute, Villa de Álvarez 28984, Mexico

7. Molecular and Structural Physiology Laboratory, School of Biological Sciences, Universidad Autónoma de Nuevo León, San Nicolás de los Garza 66455, Mexico

8. Molecular Medicine Laboratory, Unidad de Medicina Humana y Ciencias de la Salud, Universidad Autónoma de Zacatecas, Zacatecas 98160, Mexico

Abstract

Background and Objectives: Gentamicin (GM) is a nephrotoxic aminoglycoside. Neutral electrolyzed saline (SES) is a compound with anti-inflammatory, antioxidant, and immunomodulatory properties. The objective of the present study was to evaluate whether kidney damage by GM can be prevented and/or reversed through the administration of SES. Materials and Methods: The study was carried out as a prospective, single-blind, five-arm, parallel-group, randomized, preclinical trial. The nephrotoxicity model was established in male BALB/c mice by administering GM at a dose of 100 mg/kg/day intraperitoneally for 30 days, concomitantly administering (+) SES or placebo (physiologic saline solution), and then administering SES for another 30 days after the initial 30 days of GM plus SES or placebo. At the end of the test, the mice were euthanized, and renal tissues were evaluated histopathologically. Results: The GM + placebo group showed significant tubular injury, interstitial fibrosis, and increased interstitial infiltrate of inflammatory cells compared with the group without GM. Tubular injury and interstitial fibrosis were lower in the groups that received concomitant GM + SES compared with the GM + placebo group. SES administration for 30 days after the GM administration periods (GM + placebo and GM + SES for 30 days) did not reduce nephrotoxicity. Conclusions: Intraperitoneal administration of SES prevents gentamicin-induced histologic nephrotoxicity when administered concomitantly, but it cannot reverse the damage when administered later.

Funder

Foundation for Cancer Ethics, Education and Research of the Cancerology State Institute, Colima, México

Publisher

MDPI AG

Subject

General Medicine

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