碳酸酐酶抑制剂和激活剂的药物相互作用。

Claudiu T Supuran
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引用次数: 0

摘要

简介:.几十年来,碳酸酐酶(CAs,EC 4.2.1.1)一直是公认的药物靶点,其抑制剂和激活剂具有相关的药理活性,并应用于各个领域。至少有 11 种磺胺类/氨基磺酸类药物被临床用作利尿剂、抗青光眼剂、抗癫痫剂或抗肥胖剂,其中一种衍生物 SLC-0111 正在作为抗肿瘤/抗转移剂进行临床试验。对激活剂的研究较少,没有临床使用的药物:对 2020 年 3 月至 2024 年 1 月期间发表的论文中 CA 抑制剂/激活剂与其他各种药物之间的药物相互作用进行了综述:涉及这些药物的药物相互作用揭示了一些有趣的发现。乙酰唑胺加环利尿剂对急性失代偿性心力衰竭有很好的疗效,而眼部疾病如X连锁视网膜脱离和黄斑水肿则可通过乙酰唑胺加贝伐单抗或外用非甾体抗炎药来治疗。在治疗淋病奈瑟菌、耐万古霉素肠球菌、蓖麻棘阿米巴原虫、螺旋体旋毛虫和新型隐球菌感染方面,乙酰唑胺和其他 CAIs 单独或与其他药物联合使用均具有强大的抗感染作用。托吡酯与芬特明联用治疗肥胖症,效果显著;唑尼沙胺与左旋多巴联用治疗帕金森病,效果显著。乙酰唑胺、甲唑胺、乙氧唑胺和 SLC-0111 与许多其他抗肿瘤药物联用,显示出协同抗肿瘤/抗转移作用。
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Drug interactions of carbonic anhydrase inhibitors and activators.

Introduction: Carbonic anhydrases (CAs, EC 4.2.1.1) have been established drug targets for decades, with their inhibitors and activators possessing relevant pharmacological activity and applications in various fields. At least 11 sulfonamides/sulfamates are clinically used as diuretics, antiglaucoma, antiepileptic, or antiobesity agents and one derivative, SLC-0111, is in clinical trials as antitumor/antimetastatic agent. The activators were less investigated with no clinically used agent.

Areas covered: Drug interactions between CA inhibitors/activators and various other agents are reviewed in publications from the period March 2020 - January 2024.

Expert opinion: Drug interactions involving these agents revealed several interesting findings. Acetazolamide plus loop diuretics is highy effective in acute decompensated heart failure, whereas ocular diseases such as X-linked retinoschisis and macular edema were treated by acetazolamide plus bevacizumab or topical NSAIDs. Potent anti-infective effects of acetazolamide and other CAIs, alone or in combination with other agents were demonstrated for the management of Neisseria gonorrhoea, vancomycin resistant enterococci, Acanthamoeba castellanii, Trichinella spiralis, and Cryptococcus neoformans infections. Topiramate, in combination with phentermine is incresingly used for the management of obesity, whereas zonisamide plus levodopa is highly effective for Parkinson's disease. Acetazolamide, methazolamide, ethoxzolamide, and SLC-0111 showed synergistic antitumor/antimetastatic action in combination with many other antitumor drugs.

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