Dodecyl creatine ester, a promising treatment to deliver creatine to neurons, achieves pharmacology efficacy in creatine transporter deficiency
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...
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Veröffentlicht in: | European journal of medicinal chemistry 2024-12, Vol.284, p.117195, Article 117195 |
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Sprache: | eng |
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Zusammenfassung: | 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.
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•Dodecyl creatine ester, a creatine prodrug passively diffuse across cell membranes regardless of the creatine transporter•DCE facilitates the delivery of creatine to neurons via the nose-to-brain pathway when administered intranasally to non-human primates•Low dose of intranasal DCE to creatine transporter deficient mice can modulate biomarkers in the brain•The strategy combining Cr prodrug and nasal administration should be relevant for the treatment of creatine transporter deficiency |
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ISSN: | 0223-5234 1768-3254 1768-3254 |
DOI: | 10.1016/j.ejmech.2024.117195 |