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Mitigating gut microbial degradation of levodopa and enhancing brain dopamine: Implications in Parkinson's disease.
- Source :
-
Communications biology [Commun Biol] 2024 May 30; Vol. 7 (1), pp. 668. Date of Electronic Publication: 2024 May 30. - Publication Year :
- 2024
-
Abstract
- Parkinson's disease is managed using levodopa; however, as Parkinson's disease progresses, patients require increased doses of levodopa, which can cause undesirable side effects. Additionally, the oral bioavailability of levodopa decreases in Parkinson's disease patients due to the increased metabolism of levodopa to dopamine by gut bacteria, Enterococcus faecalis, resulting in decreased neuronal uptake and dopamine formation. Parkinson's disease patients have varying levels of these bacteria. Thus, decreasing bacterial metabolism is a promising therapeutic approach to enhance the bioavailability of levodopa in the brain. In this work, we show that Mito-ortho-HNK, formed by modification of a naturally occurring molecule, honokiol, conjugated to a triphenylphosphonium moiety, mitigates the metabolism of levodopa-alone or combined with carbidopa-to dopamine. Mito-ortho-HNK suppresses the growth of E. faecalis, decreases dopamine levels in the gut, and increases dopamine levels in the brain. Mitigating the gut bacterial metabolism of levodopa as shown here could enhance its efficacy.<br /> (© 2024. The Author(s).)
- Subjects :
- Animals
Male
Antiparkinson Agents metabolism
Antiparkinson Agents administration & dosage
Antiparkinson Agents pharmacology
Carbidopa
Humans
Biphenyl Compounds metabolism
Mice
Organophosphorus Compounds metabolism
Mice, Inbred C57BL
Levodopa metabolism
Levodopa administration & dosage
Gastrointestinal Microbiome drug effects
Dopamine metabolism
Parkinson Disease drug therapy
Parkinson Disease metabolism
Parkinson Disease microbiology
Brain metabolism
Brain drug effects
Enterococcus faecalis metabolism
Enterococcus faecalis drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 2399-3642
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Communications biology
- Publication Type :
- Academic Journal
- Accession number :
- 38816577
- Full Text :
- https://doi.org/10.1038/s42003-024-06330-2