Evidence for an expanded time-window to mitigate a reactivated fear memory by tamoxifen

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• 作者：Thiago R. da Silva^a ; Reinaldo N. Takahashi^b ; Leandro J. Bertoglio^b ; Roberto Andreatini^a ; Cristina A.J. Stern^a ; ^{cristinastern.cs@gmail.com" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Memory reconsolidation ; Memory persistence ; Protein kinase C ; Tamoxifen
• 刊名：European Neuropsychopharmacology
• 出版年：2016
• 出版时间：October 2016
• 年：2016
• 卷：26
• 期：10
• 页码：1601-1609
• 全文大小：1004 K

文摘

The mechanisms underpinning the persistence of emotional memories are inaccurately understood. Advancing the current level of understanding with regards to this aspect is of potential translational value for the treatment of post-traumatic stress disorder (PTSD), which stems from an abnormal aversive memory formation. Tamoxifen (TMX) is a drug used in chemotherapy for breast cancer and associated with poor cognitive performances. The present study investigated whether the systemic administration of TMX (1.0–50 mg/kg) during and/or beyond the reconsolidation time-window could attenuate a reactivated contextual fear memory in laboratory animals. When administered 0, 6 or 9 h (but not 12 h) post-memory retrieval and reactivation, TMX (50 mg/kg) reduced the freezing behavior in male rats re-exposed to the paired context on day 7, but not on day 1, suggesting a specific impairing effect on memory persistence. Importantly, this effect lasts up to 21 days, but it is prevented by omitting the memory retrieval or memory reactivation. When female rats in the diestrous or proestrous phase were used, the administration of TMX 6 h after retrieving and reactivating the fear memory also impaired its persistence. Altogether, regardless of the gender, the present results indicate that the TMX is able to disrupt the persistence of reactivated fear memories in an expanded time-window, which could shed light on a new promising therapeutic strategy for PTSD.