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Dodecyl creatine ester, a promising treatment to deliver creatine to neurons, achieves pharmacology efficacy in creatine transporter deficiency.

European journal of medicinal chemistry
February 15, 2025
Clémence Disdier et al. (10 authors)
Journal ArticleHuman StudyAnimal Study
Study Details

Study Goal

The researchers aimed to evaluate the cerebral distribution and neuronal effects of Dodecyl creatine ester (DCE) administered intranasally for treating brain diseases like creatine transporter deficiency (CTD).

Results Summary

The study found that intranasal DCE achieved significant cerebral distribution in neurons and modulated neuronal markers related to cognitive function in animal models, including CTD mice and non-human primates.

Population

Wild-type non-human primates and creatine transporter deficient mice.

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (2)
InterventionDirectionEndpointPopulationDosageImpactClaim #
formulated Dodecyl creatine ester (DCE)
increase
cerebral distribution
various animal models, including wild-type non-human primates and creatine transporter deficient mice
-
achieves significant cerebral distribution up to the target cells, the neurons
#1
formulated Dodecyl creatine ester (DCE)
neutral
expression of neuronal markers related to cognitive function
various animal models, including wild-type non-human primates and creatine transporter deficient mice
-
modulates the expression of neuronal markers related to cognitive function
#2
Abstract

Dodecyl creatine ester (DCE) is a creatine prodrug currently developed for brain diseases, including creatine transporter deficiency (CTD), an incurable rare genetic disease. A dual strategy combining a prodrug to bypass the non-functional creatine transporter and its delivery via the nose-to-brain pathway has been proposed to replenish creatine levels in cerebral cells, particularly in neurons of CTD patients. In vitro and in vivo studies in various animal models, including wild-type non-human primates and creatine transporter deficient mice, show that formulated DCE, when administered intranasally, achieves significant cerebral distribution up to the target cells, the neurons, and modulates the expression of neuronal markers related to cognitive function at doses intended for patients. These compelling results contribute to a better understanding of the pharmacokinetics and pharmacodynamics of DCE after nasal administration, with a particular focus on the crucial role of the nose-to-brain pathway in DCE distribution.

Medical Subject Headings (MeSH)
AnimalsCreatineNeuronsMiceX-Linked Intellectual DisabilityHumansProdrugsAdministration, IntranasalMembrane Transport ProteinsMolecular StructureEstersDose-Response Relationship, DrugBrain Diseases, Metabolic, InbornBrainPlasma Membrane Neurotransmitter Transport Proteins
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality90/10
Research Impact Scores
APT Score0.05
Weight Score1.40
Normalized Score0.72
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