Safari Saeid, Motavaf Mahsa, Seyed Siamdoust Seyed Alireza, Alavian Seyed Moayed
Department of Anesthesiology and Pain Medicine, Iran University of Medical Sciences, Tehran, IR Iran.
Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, IR Iran ; Department of Molecular Hepatology, Middle East Liver Disease Center, Tehran, IR Iran.
Iran Red Crescent Med J. 2014 Sep 5;16(9):e20153. doi: 10.5812/ircmj.20153. eCollection 2014 Sep.
Halogenated inhalational anesthetics are currently the most common drugs used for the induction and maintenance of general anesthesia. Postoperative hepatic injury has been reported after exposure to these agents. Based on much evidence, mechanism of liver toxicity is more likely to be immunoallergic. The objective of this review study was to assess available studies on hepatotoxicity of these anesthetics.
We searched PubMed, Google Scholar, Scopus, Index Copernicus, EBSCO and the Cochrane Database using the following keywords: "inhalational Anesthetics" and "liver injury"; "inhalational anesthetics" and "hepatotoxicity"; "volatile anesthetics" and "liver injury"; "volatile anesthetics" and hepatotoxicity for the period of 1966 to 2013. Fifty two studies were included in this work.
All halogenated inhalational anesthetics are associated with liver injury. Halothane, enflurane, isoflurane and desflurane are metabolized through the metabolic pathway involving cytochrome P-450 2E1 (CYP2E1) and produce trifluoroacetylated components; some of which may be immunogenic. The severity of hepatotoxicity is associated with the degree by which they undergo hepatic metabolism by this cytochrome. However, liver toxicity is highly unlikely from sevoflurane as is not metabolized to trifluoroacetyl compounds.
Hepatotoxicity of halogenated inhalational anesthetics has been well documented in available literature. Halothane-induced liver injury was extensively acknowledged; however, the next generation halogenated anesthetics have different molecular structures and associated with less hepatotoxicity. Although anesthesia-induced hepatitis is not a common occurrence, we must consider the association between this disorder and the use of halogenated anesthetics.
卤化吸入麻醉剂是目前用于全身麻醉诱导和维持的最常用药物。接触这些药物后曾有术后肝损伤的报道。基于大量证据,肝毒性机制更可能是免疫过敏。本综述研究的目的是评估关于这些麻醉剂肝毒性的现有研究。
我们使用以下关键词在PubMed、谷歌学术、Scopus、哥白尼索引、EBSCO和考克兰数据库中进行检索:“吸入麻醉剂”和“肝损伤”;“吸入麻醉剂”和“肝毒性”;“挥发性麻醉剂”和“肝损伤”;“挥发性麻醉剂”和“肝毒性”,检索时间为1966年至2013年。本研究纳入了52项研究。
所有卤化吸入麻醉剂均与肝损伤有关。氟烷、恩氟烷、异氟烷和地氟烷通过涉及细胞色素P - 450 2E1(CYP2E1)的代谢途径进行代谢,并产生三氟乙酰化成分;其中一些可能具有免疫原性。肝毒性的严重程度与它们通过这种细胞色素进行肝代谢的程度相关。然而,七氟烷极不可能导致肝毒性,因为它不会代谢为三氟乙酰化合物。
卤化吸入麻醉剂的肝毒性在现有文献中已有充分记载。氟烷引起的肝损伤已得到广泛认可;然而,新一代卤化麻醉剂具有不同的分子结构,且肝毒性较小。尽管麻醉引起的肝炎并不常见,但我们必须考虑这种疾病与卤化麻醉剂使用之间的关联。