Matches in SemOpenAlex for { <https://semopenalex.org/work/W2496574779> ?p ?o ?g. }
- W2496574779 endingPage "203" @default.
- W2496574779 startingPage "194" @default.
- W2496574779 abstract "The human dopamine D4 receptor (hD4R) variants with long tandem repeats in the third intracellular loop have been strongly associated with attention deficit hyperactivity disorder (ADHD) and risk taking behaviors. To understand the potential molecular mechanism underlying the connection, we have investigated the synaptic function of human D4R polymorphism by virally expressing the ADHD-linked 7-repeat allele, hD4.7, or its normal counterpart, hD4.4, in the prefrontal cortex (PFC) of D4R knockout mice. We found that hD4R bound to the SH3 domain of PSD-95 in a state-dependent manner. Activation of hD4.7 caused more reduction of NR1/PSD-95 binding and NR1 surface expression than hD4.4 in PFC slices. Moreover, the NMDAR-mediated excitatory postsynaptic currents (NMDAR-EPSC) in PFC pyramidal neurons were suppressed to a larger extent by hD4.7 than hD4.4 activation. Direct stimulation of NMDARs with the partial agonist d-cycloserine prevented the NMDAR hypofunction induced by hD4.7 activation. Moreover, hD4.7-expressing mice exhibited the increased exploratory and novelty seeking behaviors, mimicking the phenotypic hallmark of human ADHD. d-cycloserine administration ameliorated the ADHD-like behaviors in hD4.7-expressing mice. Our results suggest that over-suppression of NMDAR function may underlie the role of hD4.7 in ADHD, and enhancing NMDAR signaling may be a viable therapeutic strategy to ADHD humans carrying the D4.7 allele." @default.
- W2496574779 created "2016-08-23" @default.
- W2496574779 creator A5006996437 @default.
- W2496574779 creator A5021915616 @default.
- W2496574779 creator A5022333584 @default.
- W2496574779 creator A5055108049 @default.
- W2496574779 creator A5075408897 @default.
- W2496574779 creator A5076452990 @default.
- W2496574779 creator A5085994735 @default.
- W2496574779 date "2016-11-01" @default.
- W2496574779 modified "2023-10-15" @default.
- W2496574779 title "The ADHD-linked human dopamine D4 receptor variant D4.7 induces over-suppression of NMDA receptor function in prefrontal cortex" @default.
- W2496574779 cites W1209980950 @default.
- W2496574779 cites W1512528002 @default.
- W2496574779 cites W1513017963 @default.
- W2496574779 cites W1558650798 @default.
- W2496574779 cites W1576992353 @default.
- W2496574779 cites W1577223111 @default.
- W2496574779 cites W1580790875 @default.
- W2496574779 cites W1678806323 @default.
- W2496574779 cites W1710761543 @default.
- W2496574779 cites W1870049385 @default.
- W2496574779 cites W1969887276 @default.
- W2496574779 cites W1972764647 @default.
- W2496574779 cites W1973138133 @default.
- W2496574779 cites W1973331389 @default.
- W2496574779 cites W1973678939 @default.
- W2496574779 cites W1975977959 @default.
- W2496574779 cites W1979179687 @default.
- W2496574779 cites W1987064543 @default.
- W2496574779 cites W1994357188 @default.
- W2496574779 cites W1998217277 @default.
- W2496574779 cites W1999567494 @default.
- W2496574779 cites W2012090610 @default.
- W2496574779 cites W2012840534 @default.
- W2496574779 cites W2016971515 @default.
- W2496574779 cites W2024469079 @default.
- W2496574779 cites W2024636649 @default.
- W2496574779 cites W2026395566 @default.
- W2496574779 cites W2028318424 @default.
- W2496574779 cites W2031534534 @default.
- W2496574779 cites W2031598294 @default.
- W2496574779 cites W2031704557 @default.
- W2496574779 cites W2035317930 @default.
- W2496574779 cites W2043117894 @default.
- W2496574779 cites W2050949077 @default.
- W2496574779 cites W2054251181 @default.
- W2496574779 cites W2064111585 @default.
- W2496574779 cites W2065938665 @default.
- W2496574779 cites W2067587687 @default.
- W2496574779 cites W2069164790 @default.
- W2496574779 cites W2069458216 @default.
- W2496574779 cites W2070005343 @default.
- W2496574779 cites W2072154257 @default.
- W2496574779 cites W2085595055 @default.
- W2496574779 cites W2086710797 @default.
- W2496574779 cites W2089742418 @default.
- W2496574779 cites W2093573816 @default.
- W2496574779 cites W2093600869 @default.
- W2496574779 cites W2094698442 @default.
- W2496574779 cites W2098273438 @default.
- W2496574779 cites W2101656405 @default.
- W2496574779 cites W2114011270 @default.
- W2496574779 cites W2114809015 @default.
- W2496574779 cites W2118200565 @default.
- W2496574779 cites W2120981636 @default.
- W2496574779 cites W2124827486 @default.
- W2496574779 cites W2130184296 @default.
- W2496574779 cites W2131958615 @default.
- W2496574779 cites W2136680209 @default.
- W2496574779 cites W2142875089 @default.
- W2496574779 cites W2147177339 @default.
- W2496574779 cites W2157787057 @default.
- W2496574779 cites W2158090573 @default.
- W2496574779 cites W2162045920 @default.
- W2496574779 cites W2162486797 @default.
- W2496574779 cites W2165235512 @default.
- W2496574779 cites W2262620469 @default.
- W2496574779 cites W228285537 @default.
- W2496574779 cites W2331220951 @default.
- W2496574779 doi "https://doi.org/10.1016/j.nbd.2016.07.024" @default.
- W2496574779 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5391260" @default.
- W2496574779 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27475724" @default.
- W2496574779 hasPublicationYear "2016" @default.
- W2496574779 type Work @default.
- W2496574779 sameAs 2496574779 @default.
- W2496574779 citedByCount "14" @default.
- W2496574779 countsByYear W24965747792017 @default.
- W2496574779 countsByYear W24965747792018 @default.
- W2496574779 countsByYear W24965747792019 @default.
- W2496574779 countsByYear W24965747792020 @default.
- W2496574779 countsByYear W24965747792021 @default.
- W2496574779 countsByYear W24965747792022 @default.
- W2496574779 countsByYear W24965747792023 @default.
- W2496574779 crossrefType "journal-article" @default.
- W2496574779 hasAuthorship W2496574779A5006996437 @default.
- W2496574779 hasAuthorship W2496574779A5021915616 @default.
- W2496574779 hasAuthorship W2496574779A5022333584 @default.