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Gut bacterial tyrosine decarboxylases restrict levels of levodopa in the treatment of Parkinson’s disease
by
Frye, Alexandra K.
, van Kessel, Sebastiaan P.
, Castejon, Maria
, El Aidy, Sahar
, van Dijk, Gertjan
, Keshavarzian, Ali
, El-Gendy, Ahmed O.
in
38/22
/ 38/77
/ 38/88
/ 631/326
/ 631/337
/ 64/86
/ 82/80
/ Abundance
/ Aged
/ Aged, 80 and over
/ Animals
/ Antiparkinson Agents - metabolism
/ Antiparkinson Agents - pharmacology
/ Bacteria
/ Bacteria - enzymology
/ Bacteria - isolation & purification
/ Bioavailability
/ Digestive system
/ Dopamine
/ Drug metabolism
/ Female
/ Gastrointestinal Microbiome - physiology
/ Gastrointestinal tract
/ Humanities and Social Sciences
/ Humans
/ Intestinal microflora
/ Intestine, Small - metabolism
/ Intestine, Small - microbiology
/ Levodopa
/ Levodopa - metabolism
/ Levodopa - pharmacokinetics
/ Male
/ Metabolism
/ Metabolites
/ Microbiota
/ Microorganisms
/ Middle Aged
/ multidisciplinary
/ Parkinson Disease - drug therapy
/ Parkinson Disease - microbiology
/ Parkinson's disease
/ Patients
/ Rats
/ Regulators
/ Relative abundance
/ Science
/ Science (multidisciplinary)
/ Small intestine
/ Substrate inhibition
/ Tyrosine
/ Tyrosine decarboxylase
/ Tyrosine Decarboxylase - metabolism
2019
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Gut bacterial tyrosine decarboxylases restrict levels of levodopa in the treatment of Parkinson’s disease
by
Frye, Alexandra K.
, van Kessel, Sebastiaan P.
, Castejon, Maria
, El Aidy, Sahar
, van Dijk, Gertjan
, Keshavarzian, Ali
, El-Gendy, Ahmed O.
in
38/22
/ 38/77
/ 38/88
/ 631/326
/ 631/337
/ 64/86
/ 82/80
/ Abundance
/ Aged
/ Aged, 80 and over
/ Animals
/ Antiparkinson Agents - metabolism
/ Antiparkinson Agents - pharmacology
/ Bacteria
/ Bacteria - enzymology
/ Bacteria - isolation & purification
/ Bioavailability
/ Digestive system
/ Dopamine
/ Drug metabolism
/ Female
/ Gastrointestinal Microbiome - physiology
/ Gastrointestinal tract
/ Humanities and Social Sciences
/ Humans
/ Intestinal microflora
/ Intestine, Small - metabolism
/ Intestine, Small - microbiology
/ Levodopa
/ Levodopa - metabolism
/ Levodopa - pharmacokinetics
/ Male
/ Metabolism
/ Metabolites
/ Microbiota
/ Microorganisms
/ Middle Aged
/ multidisciplinary
/ Parkinson Disease - drug therapy
/ Parkinson Disease - microbiology
/ Parkinson's disease
/ Patients
/ Rats
/ Regulators
/ Relative abundance
/ Science
/ Science (multidisciplinary)
/ Small intestine
/ Substrate inhibition
/ Tyrosine
/ Tyrosine decarboxylase
/ Tyrosine Decarboxylase - metabolism
2019
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Gut bacterial tyrosine decarboxylases restrict levels of levodopa in the treatment of Parkinson’s disease
by
Frye, Alexandra K.
, van Kessel, Sebastiaan P.
, Castejon, Maria
, El Aidy, Sahar
, van Dijk, Gertjan
, Keshavarzian, Ali
, El-Gendy, Ahmed O.
in
38/22
/ 38/77
/ 38/88
/ 631/326
/ 631/337
/ 64/86
/ 82/80
/ Abundance
/ Aged
/ Aged, 80 and over
/ Animals
/ Antiparkinson Agents - metabolism
/ Antiparkinson Agents - pharmacology
/ Bacteria
/ Bacteria - enzymology
/ Bacteria - isolation & purification
/ Bioavailability
/ Digestive system
/ Dopamine
/ Drug metabolism
/ Female
/ Gastrointestinal Microbiome - physiology
/ Gastrointestinal tract
/ Humanities and Social Sciences
/ Humans
/ Intestinal microflora
/ Intestine, Small - metabolism
/ Intestine, Small - microbiology
/ Levodopa
/ Levodopa - metabolism
/ Levodopa - pharmacokinetics
/ Male
/ Metabolism
/ Metabolites
/ Microbiota
/ Microorganisms
/ Middle Aged
/ multidisciplinary
/ Parkinson Disease - drug therapy
/ Parkinson Disease - microbiology
/ Parkinson's disease
/ Patients
/ Rats
/ Regulators
/ Relative abundance
/ Science
/ Science (multidisciplinary)
/ Small intestine
/ Substrate inhibition
/ Tyrosine
/ Tyrosine decarboxylase
/ Tyrosine Decarboxylase - metabolism
2019
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Gut bacterial tyrosine decarboxylases restrict levels of levodopa in the treatment of Parkinson’s disease
Journal Article
Gut bacterial tyrosine decarboxylases restrict levels of levodopa in the treatment of Parkinson’s disease
2019
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Overview
Human gut microbiota senses its environment and responds by releasing metabolites, some of which are key regulators of human health and disease. In this study, we characterize gut-associated bacteria in their ability to decarboxylate levodopa to dopamine via tyrosine decarboxylases. Bacterial tyrosine decarboxylases efficiently convert levodopa to dopamine, even in the presence of tyrosine, a competitive substrate, or inhibitors of human decarboxylase. In situ levels of levodopa are compromised by high abundance of gut bacterial tyrosine decarboxylase in patients with Parkinson’s disease. Finally, the higher relative abundance of bacterial tyrosine decarboxylases at the site of levodopa absorption, proximal small intestine, had a significant impact on levels of levodopa in the plasma of rats. Our results highlight the role of microbial metabolism in drug availability, and specifically, that abundance of bacterial tyrosine decarboxylase in the proximal small intestine can explain the increased dosage regimen of levodopa treatment in Parkinson’s disease patients.
The gut microbiota can impact the bioavailability of therapeutic drugs. Here, the authors show that bacterial tyrosine decarboxylases (TDC) decrease the levels of levodopa, the primary treatment in Parkinson’s disease, by conversion to dopamine, and suggest TDC as a potential predictive biomarker for treatment.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 38/77
/ 38/88
/ 631/326
/ 631/337
/ 64/86
/ 82/80
/ Aged
/ Animals
/ Antiparkinson Agents - metabolism
/ Antiparkinson Agents - pharmacology
/ Bacteria
/ Bacteria - isolation & purification
/ Dopamine
/ Female
/ Gastrointestinal Microbiome - physiology
/ Humanities and Social Sciences
/ Humans
/ Intestine, Small - metabolism
/ Intestine, Small - microbiology
/ Levodopa
/ Male
/ Parkinson Disease - drug therapy
/ Parkinson Disease - microbiology
/ Patients
/ Rats
/ Science
/ Tyrosine
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