Chua Eng Wee, Harger Simon P, Kennedy Martin A
Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Hawke's Bay District Health Board, Hastings, New Zealand.
Front Pharmacol. 2019 Aug 22;10:931. doi: 10.3389/fphar.2019.00931. eCollection 2019.
We report two cases of metoclopramide-induced acute dystonia in pregnant women and consider the role of genetic variation in the pathogenesis of the adverse effect. By whole-gene sequencing, we found that both women were CYP2D6 poor metabolizers. We theorize that CYP2D6 governs the risk of metoclopramide-related acute dystonia through its role in the synthesis of serotonin, which inhibits the dopamine tone. The effect of CYP2D6 poor metabolism is exaggerated by rises in the estrogen levels during pregnancy, as the hormone augments dopamine sensitivity. Together, the two factors may create a hyper-dopaminergic state that is easily upset by metoclopramide, resulting in acute dystonia.
我们报告了两例孕妇因服用胃复安引发急性肌张力障碍的病例,并探讨了基因变异在该不良反应发病机制中的作用。通过全基因测序,我们发现这两名女性均为细胞色素P450 2D6(CYP2D6)慢代谢者。我们推测,CYP2D6通过其在血清素合成中的作用来控制胃复安相关急性肌张力障碍的风险,血清素会抑制多巴胺能张力。孕期雌激素水平升高会加剧CYP2D6慢代谢的影响,因为该激素会增强多巴胺敏感性。这两个因素共同作用,可能会导致一种高多巴胺能状态,这种状态很容易因胃复安而失衡,从而引发急性肌张力障碍。