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Slow-release delivery enhances the pharmacological properties of oral 5-hydroxytryptophan: mouse proof-of-concept
by
Urs, Nikhil M
, Yi Zixuan
, Windermere Sonora A
, Sachs, Benjamin D
, Caron, Marc G
, Cajina Manuel
, Roberts, Wendy L
, Royer, Elizabeth L
, Oh Adrianna
, Bangle Rachel
, Modesto, Nathan
, Nicholls, Peter J
, Snyder, Joshua C
, Jacobsen, Jacob P
, Vernon, Rebecca
in
Antidepressants
/ Fluoxetine
/ Gene expression
/ Pharmacodynamics
/ Pharmacokinetics
/ Serotonin uptake inhibitors
2019
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Slow-release delivery enhances the pharmacological properties of oral 5-hydroxytryptophan: mouse proof-of-concept
by
Urs, Nikhil M
, Yi Zixuan
, Windermere Sonora A
, Sachs, Benjamin D
, Caron, Marc G
, Cajina Manuel
, Roberts, Wendy L
, Royer, Elizabeth L
, Oh Adrianna
, Bangle Rachel
, Modesto, Nathan
, Nicholls, Peter J
, Snyder, Joshua C
, Jacobsen, Jacob P
, Vernon, Rebecca
in
Antidepressants
/ Fluoxetine
/ Gene expression
/ Pharmacodynamics
/ Pharmacokinetics
/ Serotonin uptake inhibitors
2019
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Slow-release delivery enhances the pharmacological properties of oral 5-hydroxytryptophan: mouse proof-of-concept
by
Urs, Nikhil M
, Yi Zixuan
, Windermere Sonora A
, Sachs, Benjamin D
, Caron, Marc G
, Cajina Manuel
, Roberts, Wendy L
, Royer, Elizabeth L
, Oh Adrianna
, Bangle Rachel
, Modesto, Nathan
, Nicholls, Peter J
, Snyder, Joshua C
, Jacobsen, Jacob P
, Vernon, Rebecca
in
Antidepressants
/ Fluoxetine
/ Gene expression
/ Pharmacodynamics
/ Pharmacokinetics
/ Serotonin uptake inhibitors
2019
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Slow-release delivery enhances the pharmacological properties of oral 5-hydroxytryptophan: mouse proof-of-concept
Journal Article
Slow-release delivery enhances the pharmacological properties of oral 5-hydroxytryptophan: mouse proof-of-concept
2019
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Overview
5-hydroxytryptophan (5-HTP) has shown therapeutic promise in a range of human CNS disorders. But native 5-HTP immediate release (IR) is poorly druggable, as rapid absorption causes rapid onset of adverse events, and rapid elimination causes fluctuating exposure. Recently, we reported that 5-HTP delivered as slow-release (SR) in mice augmented the brain pro-serotonergic effect of selective serotonin reuptake inhibitors (SSRIs), without the usual adverse events associated with 5-HTP IR. However, our previous study entailed translational limitations, in terms of route, dose, and duration. Here we modeled oral 5-HTP SR in mice by administering 5-HTP via the food. We modeled oral SSRI treatment via fluoxetine in the water, in a regimen recapitulating clinical pharmacokinetics and pharmacodynamics. 5-HTP SR produced plasma 5-HTP levels well within the range enhancing brain 5-HT function in humans. 5-HTP SR robustly increased brain 5-HT synthesis and levels. When administered with an SSRI, 5-HTP SR enhanced 5-HT-sensitive behaviors and neurotrophic mRNA expression. 5-HTP SR’s pro-serotonergic effects were stronger in mice with endogenous brain 5-HT deficiency. In a comprehensive screen, 5-HTP SR was devoid of overt toxicological effects. The present preclinical data, appreciated in the context of published 5-HTP clinical data, suggest that 5-HTP SR could represent a new therapeutic approach to the plethora of CNS disorders potentially treatable with a pro-serotonergic drug. 5-HTP SR might in particular be therapeutically relevant when brain 5-HT deficiency is pathogenic and as an adjunctive augmentation therapy to SSRI therapy.
Publisher
Nature Publishing Group
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