首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >Effects of tenoxicam on renal function and the disposition of inulin and p-aminohippurate in healthy volunteers and patients with chronic renal failure.
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Effects of tenoxicam on renal function and the disposition of inulin and p-aminohippurate in healthy volunteers and patients with chronic renal failure.

机译:替诺昔康对健康志愿者和慢性肾功能衰竭患者肾功能以及菊粉和对氨基马尿酸分布的影响。

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摘要

1. The effects of tenoxicam on renal function were studied in 10 patients with chronic renal failure (creatinine clearance 46.7 +/- 11.9 ml min-1 1.73 m-2) and eight healthy volunteers. A parallel treatment control group of eight healthy volunteers received placebo. Tenoxicam was given orally in a dose of 40 mg daily for 2 days followed by 20 mg daily for a further 8 days. Renal function was assessed by measurement of the renal clearances of inulin and p-aminohippurate (PAH) using the single injection technique before and during administration of tenoxicam. 2. In the healthy volunteers there were no changes in glomerular filtration rate, effective renal plasma flow, or the urinary excretion of N-acetylglucosaminidase and beta 2-microglobulin on the 3rd and 10th days of treatment with tenoxicam. The mean urinary excretion of prostaglandins E2 and 6-keto F1 alpha decreased during treatment but there was great individual variation and the differences were not statistically significant. Tenoxicam had no effect on the half-life, clearance, volume of distribution or urinary recovery of inulin and PAH. 3. There was no significant change in the clearance of inulin and creatinine after treatment with tenoxicam for 10 days in the patients with chronic renal failure. However, in this group there was a significant increase in plasma creatinine on the 3rd and 6th days with a return to pretreatment levels by the 10th day. The administration of tenoxicam for 10 days was associated with a small but significant increase in the plasma half-life and volume of distribution of inulin.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在十名慢性肾功能衰竭(肌酐清除率46.7 +/- 11.9 ml min-1 1.73 m-2)和八名健康志愿者中研究了替诺昔康对肾功能的影响。由八名健康志愿者组成的平行治疗对照组接受了安慰剂。口服替诺昔康的剂量为每天40 mg,持续2天,然后每天20 mg,持续8天。在替诺昔康给药之前和期间,通过单次注射技术测量菊粉和对氨基马尿酸盐(PAH)的肾脏清除率,评估肾功能。 2.在健康的志愿者中,使用替诺昔康治疗的第3天和第10天,肾小球滤过率,有效肾血浆流量或N-乙酰氨基葡萄糖苷酶和β2-微球蛋白的尿排泄没有变化。治疗期间前列腺素E2和6-酮F1α的平均尿排泄减少,但个体差异很大,差异无统计学意义。替诺昔康对菊粉和PAH的半衰期,清除率,分布量或尿回收率没有影响。 3.慢性肾功能衰竭患者使用替诺昔康治疗10天后,菊粉和肌酐的清除率无明显变化。但是,在该组中,第3天和第6天血浆肌酐显着增加,第10天恢复到治疗前水平。替诺昔康给药10天与血浆半衰期和菊粉分布量的小幅但显着增加有关(摘要截短为250字)

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