Modulation of Serotonin Receptors in Neurodevelopmental Disorders: Focus on 5-HT7 Receptor

Authors
Lee, JieonAvramets, DianaJeon, ByungsunChoo, Hyunah
Issue Date
2021-06
Publisher
MDPI
Citation
MOLECULES, v.26, no.11
Abstract
Since neurodevelopmental disorders (NDDs) influence more than 3% of children worldwide, there has been intense investigation to understand the etiology of disorders and develop treatments. Although there are drugs such as aripiprazole, risperidone, and lurasidone, these medications are not cures for the disorders and can only help people feel better or alleviate their symptoms. Thus, it is required to discover therapeutic targets in order to find the ultimate treatments of neurodevelopmental disorders. It is suggested that abnormal neuronal morphology in the neurodevelopment process is a main cause of NDDs, in which the serotonergic system is emerging as playing a crucial role. From this point of view, we noticed the correlation between serotonin receptor subtype 7 (5-HT7R) and NDDs including autism spectrum disorder (ASD), fragile X syndrome (FXS), and Rett syndrome (RTT). 5-HT7R modulators improved altered behaviors in animal models and also affected neuronal morphology via the 5-HT7R/G(12) signaling pathway. Through the investigation of recent studies, it is suggested that 5-HT7R could be a potential therapeutic target for the treatment of NDDs.
Keywords
BRAIN MITOCHONDRIAL DYSFUNCTION; HETEROTRIMERIC G-PROTEINS; AUTISM-LIKE DEFICITS; MOUSE MODEL; SYNAPTIC PLASTICITY; RETT-SYNDROME; RHO GTPASES; FEMALE MICE; PHARMACOLOGICAL STIMULATION; GENE-TRANSCRIPTION; BRAIN MITOCHONDRIAL DYSFUNCTION; HETEROTRIMERIC G-PROTEINS; AUTISM-LIKE DEFICITS; MOUSE MODEL; SYNAPTIC PLASTICITY; RETT-SYNDROME; RHO GTPASES; FEMALE MICE; PHARMACOLOGICAL STIMULATION; GENE-TRANSCRIPTION; serotonin receptor; 5-HT7R; neurodevelopmental disorders; autism spectrum disorder; fragile X syndrome; Rett syndrome
ISSN
1420-3049
URI
https://pubs.kist.re.kr/handle/201004/116932
DOI
10.3390/molecules26113348
Appears in Collections:
KIST Article > 2021
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