Pendergraft William F, Herlitz Leal C, Thornley-Brown Denyse, Rosner Mitchell, Niles John L
UNC Kidney Center, Division of Nephrology and Hypertension, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; Division of Nephrology, Department of Medicine, and Vasculitis and Glomerulonephritis Clinic, Division of Nephrology, Massachusetts General Hospital, Boston, Massachusetts;
Division of Renal Pathology, Department of Pathology and Cell Biology, Columbia University Medical Center, New York, New York;
Clin J Am Soc Nephrol. 2014 Nov 7;9(11):1996-2005. doi: 10.2215/CJN.00360114. Epub 2014 Jul 17.
The kidneys can be injured in diverse ways by many drugs, both legal and illegal. Novel associations and descriptions of nephrotoxic effects of common and emerging drugs of abuse have appeared over the past several years. Anabolic androgenic steroids, illicitly used by athletes and others for decades to increase muscle mass and decrease body fat, are emerging as podocyte toxins given recent descriptions of severe forms of FSGS in long-term abusers. Synthetic cannabinoids, a new group of compounds with marijuana-like effects, recently became popular as recreational drugs and have been associated with an atypical form of AKI. 3,4-Methylenedioxymethamphetamine, commonly known as ecstasy, is a widely used synthetic recreational drug with mood-enhancing properties and a constellation of toxicities that can result in death. These toxic effects include hyperthermia, hypotonic hyponatremia due to its arginine vasopressin secretagogue-like effects, rhabdomyolysis, and cardiovascular collapse. Cocaine, a serotonin-norepinephrine-dopamine reuptake inhibitor that serves as an illegal stimulant, appetite suppressant, and anesthetic, also causes vasoconstriction and rhabdomyolysis. Recent adulteration of much of the world's supply of cocaine with levamisole, an antihelminthic agent with attributes similar to but distinct from those of cocaine, appears to have spawned a new type of ANCA-associated systemic vasculitis. This review discusses the nephrotoxic effects of these common and emerging drugs of abuse, of which both community and health care providers should become aware given their widespread abuse. Future investigation into pathogenetic mechanisms associated with these drugs is critical and may provide a window into ways to lessen and even prevent the nephrotoxic effects of these drugs of abuse and perhaps allow a deeper understanding of the nephrotoxicities themselves.
肾脏可能会因许多合法和非法药物而受到不同方式的损伤。在过去几年中,出现了关于常见和新型滥用药物肾毒性作用的新关联和描述。合成代谢雄激素类固醇,被运动员和其他人非法使用数十年以增加肌肉量和减少体脂,鉴于近期对长期滥用者中严重形式的局灶节段性肾小球硬化的描述,正成为足细胞毒素。合成大麻素,一类具有类似大麻效果的新化合物,最近作为消遣性药物流行起来,并与一种非典型形式的急性肾损伤有关。3,4-亚甲基二氧甲基苯丙胺,俗称摇头丸,是一种广泛使用的具有情绪增强特性和一系列可导致死亡的毒性的合成消遣性药物。这些毒性作用包括体温过高、因其类似精氨酸加压素分泌促进剂的作用导致的低渗性低钠血症、横纹肌溶解和心血管衰竭。可卡因,一种血清素-去甲肾上腺素-多巴胺再摄取抑制剂,用作非法兴奋剂、食欲抑制剂和麻醉剂,也会导致血管收缩和横纹肌溶解。最近世界上大部分可卡因供应被左旋咪唑掺假,左旋咪唑是一种驱虫剂,其属性与可卡因相似但又不同,这似乎引发了一种新型的抗中性粒细胞胞浆抗体相关性系统性血管炎。本综述讨论了这些常见和新型滥用药物的肾毒性作用,鉴于它们的广泛滥用,社区和医疗保健提供者都应该了解。对与这些药物相关的发病机制进行未来研究至关重要,可能会为减轻甚至预防这些滥用药物的肾毒性作用的方法提供一个窗口,也许还能更深入地了解肾毒性本身。