Abstract
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.
Original language | English |
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Pages (from-to) | 361-374 |
Number of pages | 14 |
Journal | Expert Opinion on Therapeutic Targets |
Volume | 26 |
DOIs | |
Publication status | Published - 2022 |
Keywords
- Brain
- Heme Oxygenase (Decyclizing)
- Heme Oxygenase-1
- Humans
- Oxidoreductases Acting on CH-CH Group Donors
- Research
- carbon monoxide
- drug research and development
- heme oxygenase
- nervous system
- neurodegeneration