| Literature DB >> 34196695 |
Michael J Hurley1,2, Robert M J Deacon3, A W Edith Chan4, David Baker5, David L Selwood4, Patricia Cogram3,6.
Abstract
Fragile X syndrome is the most common inherited intellectual disability and mono-genetic cause of autism spectrum disorder. It is a neurodevelopmental condition occurring due to a CGG trinucleotide expansion in the FMR1 gene. Polymorphisms and variants in large-conductance calcium-activated potassium channels are increasingly linked to intellectual disability and loss of FMR protein causes reduced large-conductance calcium-activated potassium channel activity leading to abnormalities in synapse function. Using the cannabinoid-like large-conductance calcium-activated potassium channel activator VSN16R we rescued behavioural deficits such as repetitive behaviour, hippocampal dependent tests of daily living, hyperactivity and memory in a mouse model of fragile X syndrome. VSN16R has been shown to be safe in a phase 1 study in healthy volunteers and in a phase 2 study in patients with multiple sclerosis with high oral bioavailability and no serious adverse effects reported. VSN16R could therefore be directly utilized in a fragile X syndrome clinical study. Moreover, VSN16R showed no evidence of tolerance, which strongly suggests that chronic VSN16R may have great therapeutic value for fragile X syndrome and autism spectrum disorder. This study provides new insight into the pathophysiology of fragile X syndrome and identifies a new pathway for drug intervention for this debilitating disorder.Entities:
Keywords: zzm321990 Fmr1 knockout mouse; BK channel; FMRP; VSN16R; fragile X syndrome
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Year: 2022 PMID: 34196695 PMCID: PMC8967084 DOI: 10.1093/brain/awab246
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 15.255