Faculty of Pharmacy, University of Toronto, 19 Russell Street, Toronto, Canada M5S 2S2.
Environ Toxicol Pharmacol. 2006 Feb;21(2):135-40. doi: 10.1016/j.etap.2005.07.003. Epub 2005 Aug 9.
Drug-induced blood dyscrasias can be either acute and predictable or delayed and unpredictable (idiosyncratic). The predictable toxicity is relatively easy to reproduce with in vitro models, although they may not work for drugs that require bioactivation. It is very unlikely that idiosyncratic blood dyscrasias can be modeled in vitro, although some drugs (or their reactive metabolites) that cause idiosyncratic reaction are toxic to bone marrow cells in vitro. Although the mechanisms of idiosyncratic reactions are poorly understood, there is evidence that most are due to reactive metabolites and some are immune-mediated. Therefore screening drugs for their bioactivation by myeloperoxidase, the major oxidative enzyme in bone marrow, may provide some measure of the risk that a drug will cause blood dyscrasias. Several examples of drug-induced idiosyncratic agranulocytosis, aplastic anemia and thrombocytopenia are presented, but better in vivo models are clearly needed to gain a clearer understanding of these adverse reactions.
药物引起的血液学紊乱可分为急性和可预测的,或迟发性和不可预测的(特发性)。可预测的毒性相对容易通过体外模型重现,尽管它们可能不适用于需要生物活化的药物。虽然一些导致特发性反应的药物(或其反应性代谢物)在体外对骨髓细胞有毒性,但体外模拟特发性血液学紊乱的可能性非常小。尽管特发性反应的机制尚不清楚,但有证据表明,大多数是由于反应性代谢物引起的,有些是免疫介导的。因此,通过髓过氧化物酶(骨髓中的主要氧化酶)筛选药物的生物活化情况,可能可以在一定程度上衡量药物引起血液学紊乱的风险。本文介绍了几种药物引起的特发性粒细胞减少症、再生障碍性贫血和血小板减少症的例子,但显然需要更好的体内模型来更清楚地了解这些不良反应。