Pharmaceutical, Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Pharmaceutical, Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran; Department of Clinical Pharmacy, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Biomed Pharmacother. 2019 Jan;109:103-111. doi: 10.1016/j.biopha.2018.10.093. Epub 2018 Nov 2.
Colistin (COL) belongs to the polymixin class of antibiotics used as the last line antibiotic against drug-resistant infections. However, nephrotoxicity is the major deleterious and dose-limiting side effect associated with COL therapy. Oxidative stress and mitochondrial impairment are suspected mechanisms involved in COL-induced nephrotoxicity. Taurine is one of the most abundant amino acids in the human body with antioxidant and mitochondria protecting properties. The current study was designed to evaluate the potential nephroprotective properties of taurine against COL-associated nephrotoxicity. Mice were treated with COL (15 mg/kg/day, i.v, for 7 consecutive days) alone or in combination with taurine (500 and 1000 mg/kg, i.p). Plasma biomarkers of nephrotoxicity in addition of kidney tissue markers of oxidative stress were evaluated. Additionally, kidney mitochondria were isolated, and several mitochondrial indices were assessed. The COL-associated renal injury was evident by a significant increase in plasma markers of renal injury including creatinine (Cr), and blood urine nitrogen (BUN). COL treatment also caused a significant increase in kidney reactive oxygen species (ROS) and lipid peroxidation (LPO). Renal GSH reservoirs and antioxidant capacity were also decreased in COL-treated animals. Mitochondrial parameters including mitochondrial dehydrogenase activity, membrane potential, GSH, and ATP were significantly decreased while mitochondrial LPO, permeabilization, and GSSG content were increased in the kidney of COL-treated mice. It was found that taurine (500 and 1000 mg/kg, i.p) treatment alleviated COL-induced oxidative stress and mitochondrial dysfunction in the kidney tissue. The data obtained from the current study suggest mitochondrial dysfunction and oxidative stress as fundamental mechanisms of renal injury induced by COL. On the other hand, taurine supplementation protected kidney through decreasing oxidative stress and regulating mitochondrial function.
黏菌素(COL)属于多黏菌素类抗生素,被用作对抗耐药感染的最后一线抗生素。然而,肾毒性是与 COL 治疗相关的主要有害和剂量限制的副作用。氧化应激和线粒体损伤被怀疑是 COL 诱导的肾毒性的相关机制。牛磺酸是人体内最丰富的氨基酸之一,具有抗氧化和保护线粒体的特性。本研究旨在评估牛磺酸对 COL 相关肾毒性的潜在肾保护作用。小鼠单独或联合牛磺酸(500 和 1000mg/kg,腹腔注射)用 COL(15mg/kg/天,静脉注射,连续 7 天)治疗。评估了肾毒性的血浆生物标志物以及氧化应激的肾脏组织标志物。此外,分离了肾脏线粒体,并评估了几种线粒体指数。COL 相关的肾损伤表现为肾损伤的血浆标志物显著增加,包括肌酐(Cr)和血尿素氮(BUN)。COL 处理还导致肾脏活性氧(ROS)和脂质过氧化(LPO)显著增加。COL 处理的动物的肾脏 GSH 储备和抗氧化能力也降低。线粒体参数包括线粒体脱氢酶活性、膜电位、GSH 和 ATP 显著降低,而肾脏中 COL 处理的小鼠的线粒体 LPO、通透性和 GSSG 含量增加。发现牛磺酸(500 和 1000mg/kg,腹腔注射)治疗可减轻 COL 诱导的肾脏组织氧化应激和线粒体功能障碍。本研究获得的数据表明,线粒体功能障碍和氧化应激是 COL 诱导的肾损伤的基本机制。另一方面,牛磺酸补充通过减少氧化应激和调节线粒体功能来保护肾脏。