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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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