4.0 Article

Persistent cognitive and dopamine transporter deficits in abstinent methamphetamine users

期刊

SYNAPSE
卷 62, 期 2, 页码 91-100

出版社

WILEY
DOI: 10.1002/syn.20471

关键词

neurotoxicity; PET; memory

资金

  1. NCRR NIH HHS [M01RR00002719] Funding Source: Medline
  2. NIAAA NIH HHS [R01 AA 12839] Funding Source: Medline
  3. NIDA NIH HHS [K24 DA00412, R01 DA09487] Funding Source: Medline
  4. NIMH NIH HHS [R01MH078175] Funding Source: Medline
  5. NINDS NIH HHS [R01 NS38927] Funding Source: Medline

向作者/读者索取更多资源

Background: Studies in abstinent methamphetamine (METH) users have demonstrated reductions in brain dopamine transporter (DAT) binding potential (BP), as well as cognitive and motor deficits, but it is not yet clear whether cognitive deficits and brain DAT reductions fully reverse with sustained abstinence, or whether behavioral deficits in METH users are related to dopamine (DA) deficits. This study was conducted to further investigate potential persistent psychomotor deficits secondary to METH abuse, and their relationship to brain DAT availability, as measured using quantitative PET methods with [C-11]WIN 35428. Methods: Twenty-two abstinent METH users and 17 healthy non-METH using controls underwent psychometric testing to test the hypothesis that METH users would demonstrate selective deficits in neuropsychiatric domains known to involve DA neurons (e.g., working memory, executive function, motor function). A subset of subjects also underwent PET scanning with [C-11]WIN 35428. Results: METH users were found to have modest deficits in short-term memory, executive function, and manual dexterity. Exploratory correlational analyses revealed that deficits in memory, but not those in executive or motor function, were associated with decreases in striatal DAT BR Conclusions: These results suggest a possible relationship between DAT BP and memory deficits in abstinent METH users, and lend support to the notion that METH produces lasting effects on central DA neurons in humans. As METH can also produce toxic effects on serotonin (5-HT) neurons, further study is needed to address the potential role of brain 5-HT depletion in cognitive deficits in abstinent METH users.

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