The brain heme oxygenase/biliverdin reductase system as a target in drug research and development

被引:5
|
作者
Mancuso, Cesare [1 ,2 ]
机构
[1] Fdn Policlin Univ A Gemelli IRCCS, Rome, Italy
[2] Univ Cattolica Sacro Cuore, Dept Healthcare Surveillance & Bioeth, Sect Pharmacol, Rome, Italy
关键词
carbon monoxide; drug research and development; heme oxygenase; nervous system; neurodegeneration; ENDOGENOUS CARBON-MONOXIDE; ZINC PROTOPORPHYRIN-IX; CENTRAL-NERVOUS-SYSTEM; OXIDATIVE STRESS; BILIVERDIN REDUCTASE; IN-VITRO; OXYGENASE SYSTEM; NITRIC-OXIDE; ISCHEMIA/REPERFUSION INJURY; MITOCHONDRIAL BIOGENESIS;
D O I
10.1080/14728222.2022.2052848
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction The heme oxygenase/biliverdin reductase (HO/BVR) system is involved in heme metabolism. The inducible isoform of HO (HO-1) and BVR both exert cytoprotective effects by enhancing cell stress response. In this context, some xenobiotics, which target HO-1, including herbal products, behave as neuroprotectants in several experimental models of neurodegeneration. Despite this, no drug having either HO-1 or BVR as a main target is currently available. Areas covered After a description of the brain HO/BVR system, the paper analyzes the main classes of drugs acting on the nervous system, with HO as second-level target, and their neuroprotective potential. Finally, the difficulties that exist for the development of drugs acting on HO/BVR and the possible ways to overcome these hurdles are examined. Expert opinion Although the limited clinical evidence has restricted the translational research on the HO/BVR system, mainly because of the dual nature of its by-products, there has been growing interest in the therapeutic potential of these enzymes. Scientists should boost the translational research on the HO/BVR system which could be supported by the significant evidence provided by preclinical studies.
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页码:361 / 374
页数:14
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