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卡锰福地吡[Ca4Mn(DPDP)5]、锰福地吡(MnDPDP)和锰基发光二极管,特别提及它们的超氧化物歧化酶模拟物和治疗特性。

Calmangafodipir [Ca4Mn(DPDP)5], mangafodipir (MnDPDP) and MnPLED with special reference to their SOD mimetic and therapeutic properties.

作者信息

Karlsson Jan Olof G, Ignarro Louis J, Lundström Ingemar, Jynge Per, Almén Torsten

机构信息

Division of Drug Research/Pharmacology, Linköping University, Linköping, Sweden.

Department of Molecular and Medical Pharmacology, University of California Los Angeles, Los Angeles, USA.

出版信息

Drug Discov Today. 2015 Apr;20(4):411-21. doi: 10.1016/j.drudis.2014.11.008. Epub 2014 Nov 20.

Abstract

Reactive oxygen species (ROS) and reactive nitrogen species (RNS) participate in pathological tissue damage. Mitochondrial manganese superoxide dismutase (MnSOD) normally keeps ROS and RNS in check. During development of mangafodipir (MnDPDP) as a magnetic resonance imaging (MRI) contrast agent, it was discovered that MnDPDP and its metabolite manganese pyridoxyl ethyldiamine (MnPLED) possessed SOD mimetic activity. MnDPDP has been tested as a chemotherapy adjunct in cancer patients and as an adjunct to percutaneous coronary intervention in patients with myocardial infarctions, with promising results. Whereas MRI contrast depends on release of Mn(2+), the SOD mimetic activity depends on Mn(2+) that remains bound to DPDP or PLED. Calmangafodipir [Ca4Mn(DPDP)5] is stabilized with respect to Mn(2+) and has superior therapeutic activity. Ca4Mn(DPDP)5 is presently being explored as a chemotherapy adjunct in a clinical multicenter Phase II study in patients with metastatic colorectal cancer.

摘要

活性氧(ROS)和活性氮(RNS)参与病理性组织损伤。线粒体锰超氧化物歧化酶(MnSOD)通常能控制ROS和RNS。在开发锰福地吡(MnDPDP)作为磁共振成像(MRI)造影剂的过程中,发现MnDPDP及其代谢产物锰吡啶基乙二胺(MnPLED)具有超氧化物歧化酶模拟活性。MnDPDP已在癌症患者中作为化疗辅助药物进行测试,并在心肌梗死患者中作为经皮冠状动脉介入治疗的辅助药物进行测试,取得了令人鼓舞的结果。虽然MRI造影依赖于Mn(2+)的释放,但超氧化物歧化酶模拟活性则依赖于仍与DPDP或PLED结合的Mn(2+)。钙锰福地吡[Ca4Mn(DPDP)5]相对于Mn(2+)更稳定,具有更好的治疗活性。目前,Ca4Mn(DPDP)5正在转移性结直肠癌患者的临床多中心II期研究中作为化疗辅助药物进行探索。

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