The impact of heme oxygenase-2 on pharmacological research: A bibliometric analysis and beyond

被引:6
|
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
bilirubin; carbon monoxide; drug research and development; gender medicine; neuroprotection; Parkinson's disease; translational pharmacology; CARBON-MONOXIDE; NITRIC-OXIDE; RAT-BRAIN; SELECTIVE-INHIBITION; LIPID-PEROXIDATION; PROTEIN EXPRESSION; MESSENGER-RNA; LOCALIZATION; BILIRUBIN; SYSTEM;
D O I
10.3389/fphar.2023.1156333
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Heme oxygenase (HO-2) is an enzyme mainly involved in the physiologic turnover of heme and intracellular gas sensing, and it is very abundant in the brain, testes, kidneys and vessels. Since 1990, when HO-2 was discovered, the scientific community has underestimated the role of this protein in health and disease, as attested by the small amount of articles published and citations received. One of the reason that have contributed to the lack of interest in HO-2 was the difficulty in upregulating or inhibiting this enzyme. However, over the last 10 years, novel HO-2 agonists and antagonists have been synthesized, and the availability of these pharmacological tools should increase the appeal of HO-2 as drug target. In particular, these agonists and antagonists could help explain some controversial aspects, such as the neuroprotective versus neurotoxic roles of HO-2 in cerebrovascular diseases. Furthermore, the discovery of HO-2 genetic variants and their involvement in Parkinson's disease, in particular in males, opens new avenues for pharmacogenetic studies in gender medicine.
引用
收藏
页数:8
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