Vitamin D Protects Against Gentamicin-Induced Kidney Damage in Rats Through Its Antioxidant and Anti-Inflammatory Effects.

IF 2.8 4区 医学 Q3 TOXICOLOGY
Elif Aksoz, Fazilet Sen Metin, Nurullah Guclu, Murat Celebi, Sinem Kantarcioglu Coskun, Oguzhan Korkut
{"title":"Vitamin D Protects Against Gentamicin-Induced Kidney Damage in Rats Through Its Antioxidant and Anti-Inflammatory Effects.","authors":"Elif Aksoz, Fazilet Sen Metin, Nurullah Guclu, Murat Celebi, Sinem Kantarcioglu Coskun, Oguzhan Korkut","doi":"10.1002/jat.4862","DOIUrl":null,"url":null,"abstract":"<p><p>Nephrotoxicity is one of the most important side effects of aminoglycosides, especially gentamicin. This study investigated the potential protective effect of vitamin D against gentamicin-induced kidney damage in rats. Forty-two male Wistar Albino rats were randomly divided into six groups. The control group received saline. The gentamicin group was treated with intraperitoneal gentamicin (100 mg/kg) for 7 days. Vitamin D (1000 IU/kg) was given to the D1 group for 1 week and to the D2 group for 2 weeks by oral gavage. The simultaneous treatment group received both gentamicin and vitamin D in combination for 1 week. In the pretreatment group, vitamin D was administered during the first week, and then gentamicin and vitamin D were administered together for the second week. At the end of the drug administration, all rats were sacrificed. Blood and kidney samples of rats were analyzed using biochemical methods. Rat kidneys were examined using electron microscopes. Both vitamin D treatments decreased gentamicin-induced elevations in MDA, TNF-α, and IL-6. In addition, in the vitamin D pretreatment group, gentamicin-induced rises in creatinine and urea, and decreases in SOD were also lessened. Ultrastructural indicators were improved, especially with vitamin D pretreatment. The anti-inflammatory and antioxidant properties of vitamin D protect against gentamicin-induced nephrotoxicity. The protective effect was considerably stronger if vitamin D was administered as a pretreatment. In conclusion, vitamin D supplementation before gentamicin treatment in the clinic may be an effective option to prevent the development of nephrotoxicity.</p>","PeriodicalId":15242,"journal":{"name":"Journal of Applied Toxicology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jat.4862","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Nephrotoxicity is one of the most important side effects of aminoglycosides, especially gentamicin. This study investigated the potential protective effect of vitamin D against gentamicin-induced kidney damage in rats. Forty-two male Wistar Albino rats were randomly divided into six groups. The control group received saline. The gentamicin group was treated with intraperitoneal gentamicin (100 mg/kg) for 7 days. Vitamin D (1000 IU/kg) was given to the D1 group for 1 week and to the D2 group for 2 weeks by oral gavage. The simultaneous treatment group received both gentamicin and vitamin D in combination for 1 week. In the pretreatment group, vitamin D was administered during the first week, and then gentamicin and vitamin D were administered together for the second week. At the end of the drug administration, all rats were sacrificed. Blood and kidney samples of rats were analyzed using biochemical methods. Rat kidneys were examined using electron microscopes. Both vitamin D treatments decreased gentamicin-induced elevations in MDA, TNF-α, and IL-6. In addition, in the vitamin D pretreatment group, gentamicin-induced rises in creatinine and urea, and decreases in SOD were also lessened. Ultrastructural indicators were improved, especially with vitamin D pretreatment. The anti-inflammatory and antioxidant properties of vitamin D protect against gentamicin-induced nephrotoxicity. The protective effect was considerably stronger if vitamin D was administered as a pretreatment. In conclusion, vitamin D supplementation before gentamicin treatment in the clinic may be an effective option to prevent the development of nephrotoxicity.

维生素D通过抗氧化和抗炎作用防止庆大霉素引起的大鼠肾损伤。
肾毒性是氨基糖苷类药物最重要的副作用之一,尤其是庆大霉素。本研究探讨了维生素D对庆大霉素所致大鼠肾损伤的潜在保护作用。42只雄性Wistar白化大鼠随机分为6组。对照组给予生理盐水治疗。庆大霉素组腹腔注射庆大霉素(100 mg/kg) 7 d。D1组灌胃给予维生素D (1000 IU/kg) 1周,D2组灌胃给予维生素D2周。同时治疗组给予庆大霉素和维生素D联合治疗,疗程1周。预处理组第1周给予维生素D治疗,第2周给予庆大霉素和维生素D联合治疗。在给药结束时,所有大鼠都被处死。采用生化方法对大鼠血液和肾脏样本进行分析。用电子显微镜观察大鼠肾脏。两种维生素D治疗均可降低庆大霉素诱导的MDA、TNF-α和IL-6升高。此外,在维生素D预处理组,庆大霉素引起的肌酐和尿素升高和SOD降低也有所减轻。超微结构指标得到改善,尤其是维生素D预处理。维生素D的抗炎和抗氧化特性可以防止庆大霉素引起的肾毒性。如果将维生素D作为预处理,其保护作用要强得多。总之,在临床上,在庆大霉素治疗前补充维生素D可能是预防肾毒性发展的有效选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信