Alavi F K, Zawada E T, Hoff K K
Department of Internal Medicine, University of South Dakota School of Medicine, Sioux Falls 57107-1570, USA.
Clin Nephrol. 1995 May;43(5):318-23.
Ketorolac tromethamine is a relatively new non-steroidal anti-inflammatory drug (NSAID), with potent analgesic activity. Similar to other NSAIDs, ketorolac has the potential to impair renal function. To assess the renal hemodynamic impact of the ketorolac in aged lean and obese rats, ketorolac was orally administered to 46-week-old lean and obese Zucker rats for two weeks. Ketorolac was mixed with rat chow in a manner to provide a dose equivalent to 15 mg/kg body weight/day. Glomerular filtration rate (GFR) and effective renal plasma flow (ERPF) were measured under anesthesia by standard inulin and p-aminohippuric acid clearance method, respectively. Urinary prostaglandin (PG) E2 excretion was measured before and after ketorolac treatment. Ketorolac treatment significantly reduced obese rat GFR (0.47 +/- 0.08 vs 0.78 +/- 0.03 ml/min/g, p < 0.002) and ERPF (1.12 +/- 0.14 vs 2.36 +/- 0.26 ml/min/g, p < 0.001) relative to obese control rats. In comparison, ketorolac did not significantly alter lean rats GFR (0.77 +/- 0.04 vs 0.91 +/- 0.06 ml/min/g) or ERPF (1.92 +/- 0.20 vs 2.48 +/- 0.15 ml/min/g) relative to lean control rats. Chronic ketorolac treatment significantly reduced hematocrit by 20 and 30 percent in lean and obese rats relative to controls, respectively. The renal vascular resistance was significantly increased with ketorolac treatment in obese rats (36 +/- 4 vs 79 +/- 14 mmHg/ml/min, p < 0.001) but not lean rats (28 +/- 3 vs 38 +/- 5 mmHg/ml/min, NS) relative to corresponding controls.(ABSTRACT TRUNCATED AT 250 WORDS)
酮咯酸氨丁三醇是一种相对较新的非甾体抗炎药(NSAID),具有强效镇痛活性。与其他NSAIDs类似,酮咯酸有损害肾功能的潜在风险。为评估酮咯酸对老年瘦型和肥胖型大鼠肾血流动力学的影响,对46周龄的瘦型和肥胖型 Zucker 大鼠口服给予酮咯酸两周。酮咯酸与大鼠饲料混合,使其剂量相当于15 mg/kg体重/天。分别通过标准菊粉和对氨基马尿酸清除率法在麻醉状态下测量肾小球滤过率(GFR)和有效肾血浆流量(ERPF)。在酮咯酸治疗前后测量尿前列腺素(PG)E2排泄量。与肥胖对照大鼠相比,酮咯酸治疗显著降低了肥胖大鼠的GFR(0.47±0.08 vs 0.78±0.03 ml/min/g,p<0.002)和ERPF(1.12±0.14 vs 2.36±0.26 ml/min/g,p<0.001)。相比之下,与瘦型对照大鼠相比,酮咯酸未显著改变瘦型大鼠的GFR(0.77±0.04 vs 0.91±0.06 ml/min/g)或ERPF(1.92±0.20 vs 2.48±0.15 ml/min/g)。与对照组相比,长期酮咯酸治疗使瘦型和肥胖型大鼠的血细胞比容分别显著降低了20%和30%。与相应对照组相比,酮咯酸治疗使肥胖大鼠的肾血管阻力显著增加(36±4 vs 79±14 mmHg/ml/min,p<0.001),但未使瘦型大鼠的肾血管阻力增加(28±3 vs 38±5 mmHg/ml/min,无显著性差异)。(摘要截断于250字)