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- W2920243519 abstract "Cocaine abuse and addiction remain highly prevalent and, unfortunately, poorly treated. It is well-known that essential aspects of cocaine’s addictive actions involve the drug’s ability to block the presynaptic dopamine (DA) transporter (DAT), thereby elevating extracellular levels of DA in brain circuits that subserve reward, reinforcement, and habit. Less well appreciated are the multiple DA-independent actions of cocaine, activities that we and others believe contribute key pieces to the puzzle of cocaine addiction, treatment, and relapse. In particular, a significant body of work points to altered serotonin (5-HT) signaling as one such component, not surprising given that, relative to DAT, cocaine acts as potently to block the 5-HT transporter (SERT) as to block DAT, and thereby elevates extracellular 5-HT levels throughout the brain when reward-eliciting DA elevations occur. To elucidate the contribution of SERT antagonism to the actions of cocaine, we engineered a mouse model that significantly reduces cocaine potency at SERT without disrupting the expression or function of SERT in vivo. In this short Perspective, we review the rationale for development of the SERT Met172 model, the studies that document the pharmacological impact of the Ile172Met substitution in vitro and in vivo, and our findings with the model that demonstrate serotonergic contributions to the genetic, physiological, and behavioral actions of cocaine." @default.
- W2920243519 created "2019-03-11" @default.
- W2920243519 creator A5022425643 @default.
- W2920243519 creator A5045573039 @default.
- W2920243519 date "2019-02-28" @default.
- W2920243519 modified "2023-10-18" @default.
- W2920243519 title "The SERT Met172 Mouse: An Engineered Model To Elucidate the Contributions of Serotonin Signaling to Cocaine Action" @default.
- W2920243519 cites W1431864939 @default.
- W2920243519 cites W1498524645 @default.
- W2920243519 cites W1506737211 @default.
- W2920243519 cites W1673358255 @default.
- W2920243519 cites W1788048136 @default.
- W2920243519 cites W1790419435 @default.
- W2920243519 cites W1919615929 @default.
- W2920243519 cites W1965447537 @default.
- W2920243519 cites W1973651679 @default.
- W2920243519 cites W1985176332 @default.
- W2920243519 cites W1995731066 @default.
- W2920243519 cites W2000904449 @default.
- W2920243519 cites W2003401347 @default.
- W2920243519 cites W2003661073 @default.
- W2920243519 cites W2004579306 @default.
- W2920243519 cites W2007178124 @default.
- W2920243519 cites W2008796635 @default.
- W2920243519 cites W2020727025 @default.
- W2920243519 cites W2020872795 @default.
- W2920243519 cites W2021277887 @default.
- W2920243519 cites W2027148405 @default.
- W2920243519 cites W2030081504 @default.
- W2920243519 cites W2032134562 @default.
- W2920243519 cites W2048966565 @default.
- W2920243519 cites W2051918534 @default.
- W2920243519 cites W2060268580 @default.
- W2920243519 cites W2060324739 @default.
- W2920243519 cites W2062550341 @default.
- W2920243519 cites W2068040290 @default.
- W2920243519 cites W2070264479 @default.
- W2920243519 cites W2079803535 @default.
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- W2920243519 cites W2082999191 @default.
- W2920243519 cites W2083623577 @default.
- W2920243519 cites W2085195794 @default.
- W2920243519 cites W2092319509 @default.
- W2920243519 cites W2095000010 @default.
- W2920243519 cites W2097300084 @default.
- W2920243519 cites W2097894221 @default.
- W2920243519 cites W2106966110 @default.
- W2920243519 cites W2107186809 @default.
- W2920243519 cites W2108304662 @default.
- W2920243519 cites W2108556733 @default.
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- W2920243519 cites W2112323466 @default.
- W2920243519 cites W2116085129 @default.
- W2920243519 cites W2120496470 @default.
- W2920243519 cites W2129495111 @default.
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- W2920243519 cites W2132455548 @default.
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- W2920243519 cites W2147968873 @default.
- W2920243519 cites W2149571723 @default.
- W2920243519 cites W2150237820 @default.
- W2920243519 cites W2152418590 @default.
- W2920243519 cites W2161236608 @default.
- W2920243519 cites W2165638796 @default.
- W2920243519 cites W2170871632 @default.
- W2920243519 cites W2170973922 @default.
- W2920243519 cites W2178312212 @default.
- W2920243519 cites W2281652274 @default.
- W2920243519 cites W2322796880 @default.
- W2920243519 cites W2461347737 @default.
- W2920243519 cites W2523185072 @default.
- W2920243519 cites W2624443697 @default.
- W2920243519 cites W2766424089 @default.
- W2920243519 cites W2798025613 @default.
- W2920243519 cites W2809720663 @default.
- W2920243519 cites W2888762370 @default.
- W2920243519 cites W2903682160 @default.
- W2920243519 cites W2905592105 @default.
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- W2920243519 doi "https://doi.org/10.1021/acschemneuro.9b00005" @default.
- W2920243519 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30817127" @default.
- W2920243519 hasPublicationYear "2019" @default.
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