Retinal pharmacodynamic and pharmacokinetic profile of cannabidiol in an in vivo model of retinal excitotoxicity
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
39892452
DOI
10.1016/j.ejphar.2025.177323
PII: S0014-2999(25)00076-7
Knihovny.cz E-zdroje
- Klíčová slova
- Amacrine cells, Cannabidiol, Excitotoxicity, Neuroprotection, Retina, Topical ocular formulation,
- MeSH
- kanabidiol * farmakokinetika farmakologie chemie aplikace a dávkování MeSH
- kaspasa 3 metabolismus MeSH
- krysa rodu Rattus MeSH
- kyselina alfa-amino-3-hydroxy-5-methyl-4-isoxazolpropionová toxicita MeSH
- modely nemocí na zvířatech MeSH
- neuroprotektivní látky * farmakokinetika farmakologie aplikace a dávkování MeSH
- nosiče léků chemie MeSH
- oxidační stres účinky léků MeSH
- potkani Wistar MeSH
- retina * účinky léků metabolismus patologie MeSH
- tyrosin analogy a deriváty metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- 3-nitrotyrosine MeSH Prohlížeč
- kanabidiol * MeSH
- kaspasa 3 MeSH
- kyselina alfa-amino-3-hydroxy-5-methyl-4-isoxazolpropionová MeSH
- neuroprotektivní látky * MeSH
- nosiče léků MeSH
- tyrosin MeSH
Cannabidiol (CBD) is one of the principal constituents of Cannabis Sativa with no psychoactive properties. CBD is a promising neuroprotective compound bearing anti-inflammatory and antioxidant properties. However, considering its low solubility, CBD delivery to the retina represents an unresolved issue. The first aim was to investigate the potential neuroprotective effects of CBD in an in vivo model of retinal excitotoxicity induced by α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA). Rats underwent intravitreal co-injection of AMPA (42 nmol) and CBD (10-4 M). The neuroprotective effect of CBD was investigated with histology and immunohistochemical evaluation of inflammatory and oxidative stress biomarkers. CBD reversed the AMPA-induced total retinal, inner nuclear layer and inner plexiform layer shrinkage and loss of amacrine cells. Moreover, CBD decreased the AMPA induced number of cleaved caspase-3, Iba-1 and nitrotyrosine (NT) positive cells. Based on this evidence, we developed a nanotechnological formulation of CBD to overcome critical issues related to its eye delivery. Particularly, nanostructured lipid carriers (NLC) loaded with CBD were prepared, optimized and characterized. Due to the optimal physicochemical characteristics, CBD-NLC3 has been selected and the in vitro release profile has been investigated. Additionally, CBD-NLC3 was topically administered to rats, and retinal CBD levels were determined. CBD-NLC3 formulation, after a single topical administration, efficiently delivered CBD in the retina (Cmax = 98 ± 25.9 ng/mg; Tmax = 60 min), showing a high translational value. In conclusion, these findings showed a good PD/PK profile of CBD warranting further pre-clinical and clinical evaluation of the new formulation for the treatment of retinal degenerative diseases.
Department of Drug Sciences University of Catania Catania Italy
Department of Experimental Medicine University of Campania Luigi Vanvitelli Naples Italy
Department of Pharmacology School of Medicine University of Crete Heraklion Crete Greece
Faculty of Medicine and Surgery University of Enna Kore Enna Italy
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