دورية أكاديمية

The Role of Nonmuscle Myosin II in Polydrug Memories and Memory Reconsolidation

التفاصيل البيبلوغرافية
العنوان: The Role of Nonmuscle Myosin II in Polydrug Memories and Memory Reconsolidation
اللغة: English
المؤلفون: Briggs, Sherri B., Hafenbreidel, Madalyn, Young, Erica J., Rumbaugh, Gavin, Miller, Courtney A.
المصدر: Learning & Memory. Sep 2018 25(9):391-398.
الإتاحة: Cold Spring Harbor Laboratory Press. 500 Sunnyside Boulevard, Woodbury, NY 11797-2924. Tel: 800-843-4388; Tel: 516-367-8800; Fax: 516-422-4097; e-mail: cshpres@cshl.edu; Web site: http://learnmem.cshlp.org
Peer Reviewed: Y
Page Count: 8
تاريخ النشر: 2018
Sponsoring Agency: National Institutes of Health (DHHS)
Contract Number: R01DA034116
UH23NS096833
R01DA03411603S1
نوع الوثيقة: Journal Articles
Reports - Research
Descriptors: Role, Memory, Genetics, Drug Therapy, Molecular Structure, Brain Hemisphere Functions, Fear, Food, Rewards, Cocaine, Stimulants, Drug Abuse, Correlation, Drug Rehabilitation, Recidivism
DOI: 10.1101/lm.046763.117
تدمد: 1072-0502
مستخلص: Using pharmacologic and genetic approaches targeting actin or the actin-driving molecular motor, nonmuscle myosin II (NMII), we previously discovered an immediate, retrieval-independent, and long-lasting disruption of methamphetamine- (METH-) and amphetamine-associated memories. A single intrabasolateral amygdala complex infusion or systemic administration of the NMII inhibitor Blebbistatin (Blebb) is sufficient to produce this disruption, which is selective, having no retrieval-independent effect on memories for fear, food reward, cocaine, or morphine. However, it was unclear if Blebb treatment would disrupt memories of other stimulants and amphetamine class drugs, such as nicotine (NIC) or mephedrone (MEPH; bath salts). Moreover, many individuals abuse multiple drugs, but it was unknown if Blebb could disrupt polydrug memories, or if the inclusion of another substance would render Blebb no longer able to disrupt METH-associated memories. Therefore, the present study had two primary goals: (1) to determine the ability of Blebb to disrupt NIC- or MEPH-associated memories, and (2) to determine the ability of METH to modify other unconditioned stimulus (US) associations' susceptibility to Blebb. To this end, using the conditional place preference model, mice were conditioned to NIC and MEPH alone or METH in combination with NIC, morphine, or foot shock. We report that, unlike METH, there was no retrieval-independent effect of Blebb on NIC- or MEPH-associated memories. However, similar to cocaine, reconsolidation of the memory for both drugs was disrupted. Further, when combined with METH administration, NIC- and morphine-, but not fear-, associated memories were rendered susceptible to disruption by Blebb. Given the high rate of polydrug use and the resurgence of METH use, these results have important implications for the treatment of substance use disorder.
Abstractor: As Provided
Number of References: 67
Entry Date: 2018
رقم الأكسشن: EJ1189876
قاعدة البيانات: ERIC
الوصف
تدمد:1072-0502
DOI:10.1101/lm.046763.117