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The Effect of Dextrose Hypotonic Vs Saline Hydration on Methotrexate-Induced Nephrotoxicity in Male and Female Rats

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Journal Adv Biomed Res
Date 2024 Mar 25
PMID 38525397
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Abstract

Background: High-dose methotrexate (HDMTX) as a cytotoxic agent might cause various side effects. Hyperhydration has been implemented as the major strategy to decrease the potential risk of toxicities induced by HDMTX. This study aims to assess the renoprotective effect of hydration with dextrose water (DW) 5% versus normal saline (N/S) 0.9% against methotrexate (MTX) induced nephrotoxicity.

Materials And Methods: This experimental animal study has been conducted on 36 Wistar rats (200-250 g) categorized into six groups, including male ( = 6) and female ( = 6) rats receiving sodium chloride 0.9% saline plus MTX, DW 5% plus MTX, or MTX alone. By the fifth day after the MTX injection, biochemical indexes were measured. The rats were also sacrificed and renal specimens were evaluated microscopically to determine kidney tissue damage (KTD).

Results: The groups were not significantly different with regard to blood urea nitrogen (BUN) ( = 0.5), creatinine (Cr) ( = 0.24), kidney weight ( = 0.34), and urine flow (UF) ( = 0.5), while KTD score was remarkably less in the hydrated groups ( < 0.001). Weight loss in DW-treated rats was significantly more than N/S-treated ones, and creatinine clearance (CrCl) and urine load (UL) of Cr were statistically similar between males and females in the control group, but significantly lower among the DW5% treated males.

Conclusion: Based on the findings of this study, hydration with N/S was superior to DW5% for the prevention from HDMTX-induced nephrotoxicity. Besides, we found insignificant differences between male versus female rats in response to the hydration for HDMTX-induced renoprotection; however, females probably benefit more.

References
1.
Medrano C, Oberic L, Puisset F, Recher C, Larrieu-Ciron D, Ysebaert L . Life-threatening complications after high-dose methotrexate and the benefits of glucarpidase as salvage therapy: a cohort study of 468 patients. Leuk Lymphoma. 2020; 62(4):846-853. DOI: 10.1080/10428194.2020.1846733. View

2.
Svahn T, Mellgren K, Harila-Saari A, Asberg A, Kanerva J, Jonsson O . Delayed elimination of high-dose methotrexate and use of carboxypeptidase G2 in pediatric patients during treatment for acute lymphoblastic leukemia. Pediatr Blood Cancer. 2016; 64(7). DOI: 10.1002/pbc.26395. View

3.
Perazella M, Rosner M . Drug-Induced Acute Kidney Injury. Clin J Am Soc Nephrol. 2022; 17(8):1220-1233. PMC: 9435983. DOI: 10.2215/CJN.11290821. View

4.
Francois M, Takagi K, Legrand R, Lucas N, Beutheu S, Bole-Feysot C . Increased Ghrelin but Low Ghrelin-Reactive Immunoglobulins in a Rat Model of Methotrexate Chemotherapy-Induced Anorexia. Front Nutr. 2016; 3:23. PMC: 4960292. DOI: 10.3389/fnut.2016.00023. View

5.
Mashayekhi-Sardoo H, Mohammadpour A, Nomani H, Sahebkar A . The effect of diabetes mellitus on pharmacokinetics, pharmacodynamics and adverse drug reactions of anticancer drugs. J Cell Physiol. 2019; 234(11):19339-19351. DOI: 10.1002/jcp.28644. View