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替诺昔康对健康志愿者和慢性肾衰竭患者肾功能及菊粉和对氨基马尿酸排泄的影响。

Effects of tenoxicam on renal function and the disposition of inulin and p-aminohippurate in healthy volunteers and patients with chronic renal failure.

作者信息

Freestone S, McAuslane J A, Prescott L F

机构信息

University Department of Clinical Pharmacology, Royal Infirmary, Edinburgh.

出版信息

Br J Clin Pharmacol. 1991 Oct;32(4):495-500. doi: 10.1111/j.1365-2125.1991.tb03937.x.

Abstract
  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)
摘要
  1. 研究了替诺昔康对10例慢性肾衰竭患者(肌酐清除率46.7±11.9 ml·min⁻¹/1.73 m²)和8名健康志愿者肾功能的影响。8名健康志愿者组成的平行治疗对照组接受安慰剂。替诺昔康口服给药,剂量为每日40 mg,连用2天,之后每日20 mg,再用8天。在替诺昔康给药前及给药期间,采用单次注射技术通过测量菊粉和对氨基马尿酸(PAH)的肾清除率来评估肾功能。2. 在健康志愿者中,替诺昔康治疗第3天和第10天时,肾小球滤过率、有效肾血浆流量或N - 乙酰葡糖胺酶和β2 - 微球蛋白的尿排泄量均无变化。治疗期间前列腺素E2和6 - 酮F1α的平均尿排泄量下降,但个体差异较大,差异无统计学意义。替诺昔康对菊粉和PAH的半衰期、清除率、分布容积或尿回收率无影响。3. 慢性肾衰竭患者用替诺昔康治疗10天后,菊粉和肌酐清除率无显著变化。然而,该组患者在第3天和第6天时血浆肌酐显著升高,到第10天恢复至治疗前水平。替诺昔康给药10天与菊粉的血浆半衰期和分布容积小幅但显著增加有关。(摘要截选至250字)

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