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抗菌药物的神经精神不良反应。

Neuropsychiatric Effects of Antimicrobial Agents.

机构信息

Department of Pharmacology, University of Patras School of Medicine, Rion, 25004, Patras, Achaea, Greece.

出版信息

Clin Drug Investig. 2017 May;37(5):423-437. doi: 10.1007/s40261-017-0498-z.

Abstract

Antimicrobial drugs used in clinical practice are selected on the basis of their selective toxicity against bacterial cells. However, all exhibit multiple offsite interactions with eukaryotic cell structures, resulting in adverse reactions during antimicrobial pharmacotherapy. A multitude of these side effects involve the nervous system as antimicrobials at clinically relevant concentrations seem to interact with many of the same molecules usually implicated in the action of psychotropic drugs. The importance of such events cannot be overstated, as the misdiagnosis of an adverse drug reaction as a symptom of a primary psychiatric or neurological disorder entails great suffering for the patient affected as well as significant costs for the healthcare system. The neuropsychiatric effects of antimicrobial drugs are extensively documented in the literature. A number of antimicrobial drugs have the potential to exert CNS effects and many are associated with stimulant, psychotomimetic and epileptogenic properties, mediated by GABA antagonism (beta-lactams, quinolones and clarithromycin), NMDA agonism (D-cycloserine, aminoglycosides, and perhaps quinolones), MAO inhibition (linezolid, metronidazole and isoniazid weakly) as well as more exotic mechanisms, as in the case of trimethoprim, isoniazid, ethambutol, rifampicin and the tetracyclines. While those effects are generally undesirable, they may also under certain circumstances be beneficial, and further research is warranted in that direction.

摘要

临床上使用的抗菌药物是根据其对细菌细胞的选择性毒性来选择的。然而,它们都表现出与真核细胞结构的多种非靶向相互作用,导致抗菌药物治疗期间出现不良反应。这些副作用很多都涉及神经系统,因为在临床相关浓度下的抗菌药物似乎与许多通常与精神药物作用有关的相同分子相互作用。这些事件的重要性怎么强调都不为过,因为将药物不良反应误诊为原发性精神或神经障碍的症状,不仅会给受影响的患者带来极大的痛苦,也会给医疗保健系统带来巨大的成本。抗菌药物的神经精神作用在文献中有广泛的记载。许多抗菌药物具有潜在的中枢神经系统作用,许多抗菌药物与兴奋剂、致幻剂和致癫痫特性有关,其介导机制为 GABA 拮抗(β-内酰胺类、喹诺酮类和克拉霉素)、NMDA 激动(D-环丝氨酸、氨基糖苷类和可能的喹诺酮类)、MAO 抑制(利奈唑胺、甲硝唑和异烟肼较弱)以及更奇特的机制,如甲氧苄啶、异烟肼、乙胺丁醇、利福平以及四环素类。虽然这些作用通常是不理想的,但在某些情况下也可能是有益的,因此需要在这方面进行进一步的研究。

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