Zareifopoulos Nicholas, Lagadinou Maria, Karela Anastasia, Kyriakopoulou Ourania, Velissaris Dimitrios
Department of Psychiatry, University of Patras, School of Health Sciences, Patras, GRC.
Emergency Department, General University Hospital of Patras, Patras, GRC.
Cureus. 2020 Aug 3;12(8):e9536. doi: 10.7759/cureus.9536.
The adverse events of antiviral drugs are dose-dependent and often reversible. The nervous system is often affected and to date, many studies have been published regarding the central nervous system toxicity of antiviral agents. They may cause significant neuropsychiatric complications, which range from mild symptoms such as irritability and difficulty sleeping to severe complications such as depression, psychosis, and painful peripheral neuropathy, side effects which may necessitate discontinuation of treatment. The pathogenetic mechanisms may involve molecular targets common to other centrally active drugs, including human monoamine oxidase-A (MAO-A), serotonin receptors, gamma-aminobutyric acid (GABA) GABA-A receptors, 5-HT2A and 5-HT2C receptors and others. Notable examples include oseltamivir which may act as MAO inhibitor and efavirenz, which has an affinity for serotonin 5-HT2 and GABA-A receptors, the serotonin transporter, the MAO enzyme, and the vesicular monoamine transporter, with subjective effects which may be similar to those of the psychedelic hallucinogen lysergic acid diethylamide (LSD). Other antiviral drugs with prominent nervous system effects include nucleoside reverse transcriptase inhibitors, which are associated with the development of peripheral neuropathy after prolonged use (an effect strongly associated with older drugs which have since fallen into disfavor such as stavudine) and interferons, which may cause depression. Clinicians should be familiar with such adverse effects in order to recognise them promptly once they occur and manage them appropriately.
抗病毒药物的不良事件具有剂量依赖性,且通常是可逆的。神经系统常受影响,迄今为止,已经发表了许多关于抗病毒药物中枢神经系统毒性的研究。它们可能导致严重的神经精神并发症,范围从易怒和睡眠困难等轻微症状到抑郁、精神病和疼痛性周围神经病变等严重并发症,这些副作用可能需要停药。发病机制可能涉及其他中枢活性药物共有的分子靶点,包括人类单胺氧化酶-A(MAO-A)、5-羟色胺受体、γ-氨基丁酸(GABA)GABA-A受体、5-HT2A和5-HT2C受体等。显著的例子包括可能作为MAO抑制剂的奥司他韦和对5-羟色胺5-HT2和GABA-A受体、5-羟色胺转运体、MAO酶和囊泡单胺转运体具有亲和力的依非韦伦,其主观效应可能类似于致幻剂麦角酸二乙胺(LSD)。其他具有显著神经系统作用的抗病毒药物包括核苷类逆转录酶抑制剂,长期使用后与周围神经病变的发生有关(这种效应与已不受青睐的旧药物如司他夫定密切相关)以及可能导致抑郁的干扰素。临床医生应熟悉此类不良反应,以便一旦发生能及时识别并妥善处理。