首页> 美国卫生研究院文献>Frontiers in Behavioral Neuroscience >Sex Differences in the Behavioral and Synaptic Consequences of a Single in vivo Exposure to the Synthetic Cannabimimetic WIN55212-2 at Puberty and Adulthood
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Sex Differences in the Behavioral and Synaptic Consequences of a Single in vivo Exposure to the Synthetic Cannabimimetic WIN55212-2 at Puberty and Adulthood

机译:青春期和成年期对合成大麻素WIN55212-2的体内暴露的行为和突触后果的性别差异

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摘要

Heavy cannabis consumption among adolescents is associated with significant and lasting neurobiological, psychological and health consequences that depend on the age of first use. Chronic exposure to cannabinoid agonists during the perinatal period or adolescence alters social behavior and prefrontal cortex (PFC) activity in adult rats. However, sex differences on social behavior as well as PFC synaptic plasticity after acute cannabinoid activation remain poorly explored. Here, we determined that the consequences of a single in vivo exposure to the synthetic cannabimimetic WIN55,212-2 differently affected PFC neuronal and synaptic functions after 24 h in male and female rats during the pubertal and adulthood periods. During puberty, single cannabinoid exposure (SCE) reduced play behavior in females but not males. In contrast, the same treatment impaired sociability in both sexes at adulthood. General exploration and memory recognition remained normal at both ages and both sexes. At the synaptic level, SCE ablated endocannabinoid-mediated synaptic plasticity in the PFC of females of both ages and heightened excitability of PFC pyramidal neurons at adulthood, while males were spared. In contrast, cannabinoid exposure was associated with impaired long-term potentiation (LTP) specifically in adult males. Together, these data indicate behavioral and synaptic sex differences in response to a single in vivo exposure to cannabinoid at puberty and adulthood.
机译:青少年大量食用大麻与严重和持久的神经生物学,心理和健康后果有关,这取决于首次使用的年龄。在围产期或青春期长期暴露于大麻素激动剂会改变成年大鼠的社交行为和前额叶皮层(PFC)活动。然而,急性大麻素激活后社会行为的性别差异以及PFC突触可塑性仍未得到很好的研究。在这里,我们确定,在青春期和成年期,雄性和雌性大鼠在24小时后对合成的大麻素WIN55,212-2进行单次体内暴露会影响PFC神经元和突触功能。在青春期,单次大麻素暴露(SCE)减少了女性而非男性的游戏行为。相反,相同的治疗方法会损害成年男女的社交能力。无论男女老少,一般的探索和记忆识别都保持正常。在突触水平,SCE消除了成年女性在PFC中内源性大麻素介导的突触可塑性,并且成年后PFC锥体神经元的兴奋性增强。相比之下,大麻素暴露与成年男性的长期增强能力(LTP)受损有关。总之,这些数据表明在青春期和成年期对大麻素的单次体内暴露引起的行为和突触性别差异。

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