Peripheralized sepiapterin reductase inhibition as a safe analgesic therapy.
Ontology highlight
ABSTRACT: The development of novel analgesics for chronic pain in the last 2 decades has proven virtually intractable, typically failing due to lack of efficacy and dose-limiting side effects. Identified through unbiased gene expression profiling experiments in rats and confirmed by human genome-wide association studies, the role of excessive tetrahydrobiopterin (BH4) in chronic pain has been validated by numerous clinical and preclinical studies. BH4 is an essential cofactor for aromatic amino acid hydroxylases, nitric oxide synthases, and alkylglycerol monooxygenase so a lack of BH4 leads to a range of symptoms in the periphery and central nervous system (CNS). An ideal therapeutic goal therefore would be to block excessive BH4 production, while preventing potential BH4 rundown. In this review, we
SUBMITTER: Cronin SJF
PROVIDER: S-EPMC10213231 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature
ACCESS DATA