Università degli Studi di Firenze, NEUROFARBA Department, Sezione di Scienze Farmaceutiche e Nutraceutiche, Via Ugo Schiff 6, 50019 Sesto Fiorentino Florence, Italy.
Department of Drug Chemistry and Technologies, Sapienza University of Rome, P.le A. Moro 5, 00185 Rome, Italy.
J Med Chem. 2023 Feb 9;66(3):1892-1908. doi: 10.1021/acs.jmedchem.2c01706. Epub 2023 Jan 26.
Pain control is among the most important healthcare services in patients affected by rheumatoid arthritis (RA), but the current therapeutic options (i.e., disease-modifying anti-rheumatic drugs) are limited by the risk of the side effects. In this context, we proposed an innovative approach based on the hybridization between carbonic anhydrase inhibitors (CAIs) and CO releasing molecules (CORMs). The resulting CAI-CORM hybrids were revealed to possess strong anti-inflammatory effects in in vitro models of diseases and to relieve ache symptoms in an in vivo RA rat model. In this work, we have deepened the study of these promising hybrids, designing a library of coumarin-based compounds, also including internal dicobalt hexacarbonyl systems. The results obtained from the CO releasing study, the CA inhibitory activity, and the in vivo pain-relief efficacy evaluation in the RA rat model confirmed the success of this strategy, allowing us to consider CAI-CORM hybrids promising anti-nociceptive agents against arthritis.
疼痛控制是类风湿关节炎(RA)患者最重要的医疗服务之一,但目前的治疗选择(即疾病修饰抗风湿药物)受到副作用风险的限制。在这方面,我们提出了一种基于碳酸酐酶抑制剂(CAIs)和 CO 释放分子(CORMs)杂交的创新方法。结果表明,所得到的 CAI-CORM 杂化物在疾病的体外模型中具有很强的抗炎作用,并在体内 RA 大鼠模型中缓解疼痛症状。在这项工作中,我们深入研究了这些有前途的杂化物,设计了一个基于香豆素的化合物库,还包括内部二羰基合钴系统。从 CO 释放研究、CA 抑制活性以及在 RA 大鼠模型中的体内止痛效果评估中获得的结果证实了这一策略的成功,使我们能够将 CAI-CORM 杂化物视为有前途的抗关节炎镇痛剂。