Dep. of Pharmacology and Toxicology, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
Dep. of Pathology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Life Sci. 2018 Sep 1;208:64-71. doi: 10.1016/j.lfs.2018.07.021. Epub 2018 Jul 17.
Nephrotoxicity is a serious adverse effect frequently encountered with aminoglycosides administration. Given the value of aminoglycosides in management of serious infections, nephro-protection is highly recommended. The current study investigated the nephro-protective effect of saxagliptin (SAXA) (12.5 mg/kg, I.P.) against gentamicin (GEN)-induced nephrotoxicity in rats. SAXA administration for 14 days conferred significant nephro-protection against GEN-induced nephrotoxicity manifested in decreased kidney/somatic index, enhanced cytoprotection and significant decrease in serum LDH activity together with functional renal improvement; significant increase in creatinine clearance with significant reduction in serum creatinine, BUN, proteinuria and albuminuria. Oxidant/antioxidants hemostasis was significantly improved with SAXA treatment with significant reduction in kidney MDA content and enhancement of GSH concentration and catalase activity. Moreover, kidney content of NO significantly declined with significant decline in kidney tumor necrosis factorα (TNFα), vascular adhesion molecule-1 (VCAM-1) and caspase-3 content. Ultimately, SAXA administration was associated with significant attenuation of GEN-induced necrotic and inflammatory changes. In conclusion; the modulatory effect of SAXA on inflammatory cytokines, its anti-apoptic properties, ameliorative impact on oxidative load and positive impact on host antioxidant defenses accounts for the observed nephro-protective impact.
肾毒性是氨基糖苷类药物治疗中经常遇到的严重不良反应。鉴于氨基糖苷类药物在严重感染治疗中的价值,强烈推荐使用肾保护剂。本研究探讨了沙格列汀(SAXA)(12.5mg/kg,腹腔注射)对氨基糖苷类药物引起的大鼠肾毒性的肾保护作用。SAXA 给药 14 天可显著减轻 GEN 诱导的肾毒性,表现为肾脏/体比降低、细胞保护增强、血清 LDH 活性显著降低以及肾功能改善;肌酐清除率显著增加,同时血清肌酐、BUN、蛋白尿和白蛋白尿显著减少。SAXA 治疗可显著改善氧化应激/抗氧化平衡,肾 MDA 含量降低,GSH 浓度和过氧化氢酶活性增强。此外,肾组织中 NO 的含量显著下降,同时肾组织肿瘤坏死因子α(TNFα)、血管细胞黏附分子-1(VCAM-1)和半胱氨酸天冬氨酸蛋白酶-3(caspase-3)的含量也显著下降。最终,SAXA 的给药与 GEN 诱导的坏死和炎症变化的显著衰减有关。总之,SAXA 对炎症细胞因子的调节作用、其抗凋亡特性、对氧化负荷的改善作用以及对宿主抗氧化防御的积极影响,解释了其观察到的肾保护作用。