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首页> 外文期刊>Japanese Journal of Pharmacology >Studies on the Nephrotoxicity of Aminoglycoside Antibiotics and Protection from These Effects (3) Protective Effect of Latamoxef against Tobramycin Nephrotoxicity and Its Protective Mechanism
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Studies on the Nephrotoxicity of Aminoglycoside Antibiotics and Protection from These Effects (3) Protective Effect of Latamoxef against Tobramycin Nephrotoxicity and Its Protective Mechanism

机译:氨基糖苷类抗生素肾毒性及其作用的研究(3)拉莫昔夫对妥布霉素肾毒性的保护作用及其保护机制

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References(27) Cited-By(12) Effect of latamoxef (LMOX) against tobramycin (TOB)-induced nephrotoxicity was studied in rats. Treatment with TOB (90 mg/kg/day, s.c.) alone resulted in marked increases in the activities of urinary enzymes such as lactate dehydrogenase, N-acetyl-β-D-glucosaminidase and lysozyme, urinary protein content and blood urea nitrogen, which peaked on the 7th or 10th day. The combination with LMOX (500, 1000 or 2000 mg/kg/day, s.c.) significantly suppressed increases in the parameters with TOB alone. The extent of this suppression roughly depended on the LMOX dosage. Although TOB alone caused pronounced histological changes such as extensive cortical proximal tubular cell necrosis, residual tubular basement membrane and cast formations in the renal cortex and medulla on the 7th day, these changes were apparently suppressed by combination with LMOX. In addition, intrarenal TOB concentrations in the rat given TOB alone were about 350, 500 and 1000 μg/g tissue wet weight at 3 hr, on day 3 and on day 5, respectively. On the other hand, there was a significant reduction (30-60%) in intrarenal TOB concentration by combination with LMOX. These results indicate that combination with LMOX obviously protects the rat kidney from TOB nephrotoxicity, and the protective effect may be partially due to suppression of intrarenal accumulation of TOB by LMOX.
机译:参考文献(27)引用了(12)在大鼠中研究了拉他莫昔(LMOX)对妥布霉素(TOB)诱导的肾毒性的作用。单独使用TOB(90 mg / kg / day,sc)进行治疗可显着提高尿酸酶的活性,如乳酸脱氢酶,N-乙酰基-β-D-氨基葡萄糖苷酶和溶菌酶,尿蛋白含量和血尿素氮在第7天或第10天达到峰值。与LMOX(500、1000或2000 mg / kg / day,s.c.)的组合可显着抑制单独使用TOB时参数的增加。这种抑制的程度大致取决于LMOX的剂量。尽管仅TOB在第7天就引起了明显的组织学改变,例如广泛的皮质近端肾小管细胞坏死,残余的肾小管基底膜和肾皮质和延髓的铸型,但这些改变显然被LMOX所抑制。另外,在单独给予TOB的大鼠中,在3小时,第3天和第5天,肾内TOB浓度分别为约350、500和1000μg/ g组织湿重。另一方面,与LMOX联合使用可使肾内TOB浓度显着降低(30-60%)。这些结果表明与LMOX的组合明显保护了大鼠肾脏免受TOB的肾毒性,并且该保护作用可能部分是由于LMOX抑制了TOB在肾内的蓄积。

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