Nature neuroscience · 2014
Presynaptic glycine receptors as a potential therapeutic target for hyperekplexia disease.
СтатьяПоддержка NIH: внешняя программаResearch Support, N.I.H., IntramuralНазвание и аннотация: Перевод пока не подготовлен
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Xiong Wei, Chen Shao-Rui, He Liming, Cheng Kejun, Zhao Yi-Lin, Chen Hong, Li De-Pei, Homanics Gregg E, Peever John, Rice Kenner C, Wu Ling-gang, Pan Hui-Lin, Zhang Li
Аннотация
Although postsynaptic glycine receptors (GlyRs) as αβ heteromers attract considerable research attention, little is known about the role of presynaptic GlyRs, likely α homomers, in diseases. Here, we demonstrate that dehydroxylcannabidiol (DH-CBD), a nonpsychoactive cannabinoid, can rescue GlyR functional deficiency and exaggerated acoustic and tactile startle responses in mice bearing point mutations in α1 GlyRs that are responsible for a hereditary startle-hyperekplexia disease. The GlyRs expressed as α1 homomers either in HEK-293 cells or at presynaptic terminals of the calyceal synapses in the auditory brainstem are more vulnerable than heteromers to hyperekplexia mutation-induced impairment. Homomeric mutants are more sensitive to DH-CBD than are heteromers, suggesting presynaptic GlyRs as a primary target. Consistent with this idea, DH-CBD selectively rescues impaired presynaptic GlyR activity and diminished glycine release in the brainstem and spinal cord of hyperekplexic mutant mice. Thus, presynaptic α1 GlyRs emerge as a potential therapeutic target for dominant hyperekplexia disease and other diseases with GlyR deficiency.
Предметные рубрики MeSH
6-Cyano-7-nitroquinoxaline-2,3-dioneAnimalsBrain StemDisease Models, AnimalExcitatory Amino Acid AntagonistsFemaleHEK293 CellsHumansIn Vitro TechniquesMaleMembrane PotentialsMiceMice, Inbred C57BLMice, Neurologic MutantsMutationNeuronsPresynaptic TerminalsReceptors, GlycineSodium Channel BlockersSpinal CordStiff-Person SyndromeTetrodotoxinValine