Elif Aksoz, Fazilet Sen Metin, Nurullah Guclu, Murat Celebi, Sinem Kantarcioglu Coskun, Oguzhan Korkut
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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.
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.