Nasrullah Mohammed Z, Eljaaly Khalid, Neamatallah Thikryat, Fahmy Usama A, Alamoudi Abdulmohsin J, Bakhsh Hussain T, Abdel-Naim Ashraf B
Department of Pharmacology and Toxicology, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Department of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Pharmaceuticals (Basel). 2022 Jun 23;15(7):782. doi: 10.3390/ph15070782.
The clinical value of colistin, a polymyxin antibiotic, is limited by its nephrotoxicity. Omeprazole is a commonly prescribed proton pump inhibitor. The current study aimed to evaluate the effects of the concomitant administration of omeprazole on colistin-induced nephrotoxicity in rats. Omeprazole significantly ameliorated colistin nephrotoxicity as evidenced by prevention in the rise in the serum level of creatinine, urea and cystactin C as well as urinary N-acetylglucosamine activity. This was confirmed by histological studies that indicated a decreased incidence of interstitial nephritis, degenerative cortical changes and collagen deposition. This was accompanied by the prevention of oxidative stress as omeprazole significantly inhibited the lipid peroxidation, glutathione depletion and enzymatic exhaustion of superoxide dismutase as well as catalase. Additionally, omeprazole inhibited the expression of interleukin-6 and tumor necrosis factor-α. Further, omeprazole inhibited the colistin-induced rise in Bax and the down-regulation of Bcl2 mRNA expression. An assessment of the serum levels of colistin revealed that omeprazole had no significant impact. However, it was observed that omeprazole significantly inhibited the accumulation of colistin in kidney tissues. In conclusion, omeprazole protects against colistin-induced nephrotoxicity. This can be attributed to, at least partly, omeprazole's anti-oxidant, anti-inflammatory and anti-apoptotic activities in addition to its ability to prevent the toxic accumulation of colistin in kidneys.
多粘菌素类抗生素黏菌素的临床价值因其肾毒性而受限。奥美拉唑是一种常用的质子泵抑制剂。本研究旨在评估同时给予奥美拉唑对黏菌素诱导的大鼠肾毒性的影响。奥美拉唑显著改善了黏菌素肾毒性,血清肌酐、尿素和胱抑素C水平升高以及尿N-乙酰葡糖胺活性的预防可证明这一点。组织学研究证实了这一点,该研究表明间质性肾炎、皮质退行性改变和胶原沉积的发生率降低。这伴随着氧化应激的预防,因为奥美拉唑显著抑制了脂质过氧化、谷胱甘肽消耗以及超氧化物歧化酶和过氧化氢酶的酶耗竭。此外,奥美拉唑抑制白细胞介素-6和肿瘤坏死因子-α的表达。此外,奥美拉唑抑制了黏菌素诱导的Bax升高和Bcl2 mRNA表达的下调。对黏菌素血清水平的评估显示,奥美拉唑没有显著影响。然而,观察到奥美拉唑显著抑制黏菌素在肾组织中的蓄积。总之,奥美拉唑可预防黏菌素诱导的肾毒性。这至少部分可归因于奥美拉唑的抗氧化、抗炎和抗凋亡活性,以及其防止黏菌素在肾脏中蓄积毒性的能力。