Legal Performance-enhancing Drugs Alter Course and Treatment of Rhabdomyolysis-induced Acute Kidney Injury

被引:0
|
作者
Hebert, Jessica F. [1 ]
Eiwaz, Mahaba B. [2 ]
Nickerson, Megan N. [2 ]
Munhall, Adam C. [1 ]
Pai, Akash A. [1 ]
Groat, Tahnee [1 ]
Andeen, Nicole K. [3 ]
Hutchens, Michael P. [1 ,2 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Anesthesiol & Perioperat Med, Portland, OR 97239 USA
[2] Portland VA Med Ctr, Operat Care Div, Portland, OR 97239 USA
[3] Oregon Hlth & Sci Univ, Dept Pathol, Portland, OR 97239 USA
基金
美国国家卫生研究院;
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; SUPPLEMENT USE; CILASTATIN; NEPHROTOXICITY;
D O I
10.1093/milmed/usad142
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Rhabdomyolysis-induced acute kidney injury (RIAKI) can interrupt physical training and increase mortality in injured warfighters. The legal performance-enhancing drugs caffeine and ibuprofen, which can cause renal injury, are widely used by service members. Whether caffeine or ibuprofen affects RIAKI is unknown. Cilastatin treatment was recently identified as an experimental treatment to prevent RIAKI at injury. To determine potential interacting factors in RIAKI treatment, we test the hypothesis that caffeine and ibuprofen worsen RIAKI and interfere with treatment. Materials and Methods In mice, RIAKI was induced by glycerol intramuscular injection. Simultaneously, mice received caffeine (3mg/kg), ibuprofen (10mg/kg), or vehicle. A second cohort received volume resuscitation (PlasmaLyte, 20mL/kg) in addition to caffeine or ibuprofen. In a third cohort, cilastatin (200mg/kg) was administered concurrently with drug and glycerol administration. Glomerular filtration rate (GFR), blood urea nitrogen (BUN), urine output (UOP), renal pathology, and renal immunofluorescence for kidney injury molecule 1 were quantified after 24hours. Results Caffeine did not worsen RIAKI; although BUN was modestly increased by caffeine administration, 24-hour GFR, UOP, and renal histopathology were similar between vehicle-treated, caffeine-treated, and caffeine+PlasmaLyte-treated mice. Ibuprofen administration greatly worsened RIAKI (GFR 14.319.5 vs. 577.4 +/- 454.6 mu L/min/100g in control, UOP 0.5 +/- 0.4 in ibuprofen-treated mice vs. 2.7 +/- 1.7mL/24h in control, and BUN 264 +/- 201 in ibuprofen-treated mice vs. 66 +/- 21mg/dL in control, P<.05 for all); PlasmaLyte treatment did not reverse this effect. Cilastatin with or without PlasmaLyte did not reverse the deleterious effect of ibuprofen in RIAKI. Conclusions Caffeine does not worsen RIAKI. The widely used performance-enhancing drug ibuprofen greatly worsens RIAKI in mice. Standard or experimental treatment of RIAKI including the addition of cilastatin to standard resuscitation is ineffective in mice with RIAKI exacerbated by ibuprofen. These findings may have clinical implications for the current therapy of RIAKI and for translational studies of novel treatment.
引用
收藏
页码:346 / 353
页数:8
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