Spermidine prevents the reinstatement of alcohol conditioned place preference

Avner Almeida Silva , Gabrielle de Morais Henriques , Victor Nascimento-Rocha , Behaim Correia Dias-Júnior , Alexia dos Anjos Santos , Alexandre Justo Oliveira Lima , Eduardo Ary Villela Marinho , Maribel Antonello Rubin , Carlos Fernando Mello
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Abstract

This study investigates whether spermidine (SPD), an endogenous polyamine, alters extinction and reinstatement of alcohol-induced conditioned place preference (CPP) in adult female Swiss mice. CPP was induced by injecting alcohol (1.8 g/kg, i.p.) and placing the animals in the drug-associated compartment for 10 min in four alternate days. During extinction, animals received vehicle or SPD (3, 10 or 30 mg/kg), and were placed in the drug-associated compartment for 10 min in 4 alternate days. Alcohol re-exposure was performed in the alcohol-paired compartment. In a second experiment, after conditioning, animals received vehicle, the N-methyl-d-aspartate (NMDA) receptor polyamine binding site antagonist arcaine (ARC, 0.1 mg/kg), SPD (10 mg/kg) or the association of both (ARC+SDP) in the drug-associated compartment. Animals were then sequentially subjected to alcohol re-exposure and a post-reexposure test. Spermidine did not alter CPP extinction, but prevented the reinstatement of CPP induced by alcohol reexposure. Arcaine prevented the effect of spermidine on alcohol-induced CPP reinstatement. The results suggest that SPD may facilitate the reconsolidation of conditioning memory, disrupting CPP. This effect seems to involve the polyamine binding site at the NMDA receptor, because it is prevented by ARC.

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亚精胺可防止酒精条件下位置偏好的恢复
本研究调查了亚精胺(SPD),一种内源性多胺,是否改变成年雌性瑞士小鼠酒精诱导的条件性位置偏好(CPP)的消退和恢复。通过注射酒精(1.8g/kg,i.p.)并在四天内将动物置于药物相关隔室中10分钟来诱导CPP。在灭绝期间,动物接受载体或SPD(3、10或30 mg/kg),并在4天内置于药物相关隔室中10分钟。在酒精配对室中进行酒精再暴露。在第二个实验中,在条件处理后,动物在药物相关室中接受载体、N-甲基-d-天冬氨酸(NMDA)受体多胺结合位点拮抗剂阿卡因(ARC,0.1mg/kg)、SPD(10mg/kg)或两者的结合(ARC+SDP)。然后依次对动物进行酒精再暴露和再暴露后测试。亚精胺不改变CPP的消退,但阻止了酒精再暴露诱导的CPP的恢复。Arcaine阻止亚精胺对酒精诱导的CPP恢复的影响。结果表明,SPD可能促进条件记忆的再巩固,破坏CPP。这种作用似乎涉及NMDA受体上的多胺结合位点,因为它被ARC阻止。
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来源期刊
Addiction neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
自引率
0.00%
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0
审稿时长
118 days
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