首页> 外文期刊>International journal of developmental neuroscience: the official journal of the International Society for Developmental Neuroscience >Sex-specific effects of CB1 receptor antagonism and stress in adolescence on anxiety, corticosterone concentrations, and contextual fear in adulthood in rats
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Sex-specific effects of CB1 receptor antagonism and stress in adolescence on anxiety, corticosterone concentrations, and contextual fear in adulthood in rats

机译:CB1受体对焦虑,皮质酮浓度对大鼠成年性焦虑,皮质酮浓度和语境恐惧的性别特异性影响

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There is a paucity of research regarding the role of endogenous cannabinoid signalling in adolescence on brain and behaviour development. We previously demonstrated effects of repeated CB1 receptor antagonism in adolescence on socioemotional behaviours and neural protein expression 24–48?h after the last drug administration in female rats, with no effect in males. Here we investigate whether greater effects would be manifested after a lengthier delay. In Experiment 1, male and female rats were administered either 1?mg / kg of the CB1 receptor-selective antagonist AM251, vehicle (VEH), or did not receive injections (NoINJ) daily on postnatal days (PND) 30–44 either alone (no adolescent confinement stress; noACS), or in tandem with 1?h ACS. On PND 70, adolescent AM251 exposure reduced anxiety in an elevated plus maze in males, irrespective of ACS, with no effects in females. On PND 73, there were no group differences in either sex in plasma corticosterone concentrations before or after 30?min of restraint stress, although injection stress resulted in higher baseline concentrations in males. Brains were collected on PND 74, with negligible effects of either AM251 or ACS on protein markers of synaptic plasticity and of the endocannabinoid system in the hippocampus and medial prefrontal cortex. In Experiment 2, rats from both sexes were treated with vehicle or AM251 on PND 30–44 and were tested for contextual fear conditioning and extinction in adulthood. AM251 females had greater fear recall than VEH females 24?h after conditioning, with no group differences in within- or between-session fear extinction. There were no group differences in long-term extinction memory, although AM251 females froze more during a reconditioning trial compared with VEH females. There were no group differences on any of the fear conditioning measures in males. Together, these findings indicate a modest, sex-specific role of CB1 receptor signalling in adolescence on anxiety-like behaviour in males and conditioned fear behaviour in females.
机译:有关于内源性大麻素信号传导在青春期对大脑和行为发展的作用的研究。我们以前证明了在雌性大鼠最后一次药物施用后的社会间隙行为和神经蛋白表达中的反复CB1受体拮抗作用对社会间隙行为和神经蛋白表达24-48℃。在这里,我们调查在延长延迟后是否会表现出更大的效果。在实验1中,将雄性和雌性大鼠施用1μmg/ kg的CB1受体选择性拮抗剂AM251,载体(载体),或者每天在后几天(PND)30-44每天没有接受注射(NOINJ) (没有青少年限制应力;诺克斯),或串联,1?H ACS。在PND 70中,青少年AM251曝光在雄性中升高的Plus迷宫中的焦虑减少,无论ACS如何,雌性没有任何影响。在PND 73上,血浆皮质酮浓度在约束压力之前或之后的血浆皮质酮浓度中的性别无群体差异,尽管注射胁迫导致雄性中的基线浓度较高。在PND 74上收集大脑,其突触塑性蛋白标志物和海马中的内瘤素体系的蛋白质标志物和内侧前额叶皮质中的蛋白质标志物的效果可忽略不计。在实验2中,两性大鼠用载体或AM251对PND 30-44进行处理,并在成年期进行了上下文恐惧调理和灭绝。 AM251女性比车辆在调理后的20岁时更大的恐惧召回,在会议内或之间没有群体差异。长期灭绝记忆没有群体差异,尽管AM251女性在与车辆女性相比,在再处理试验期间僵硬了。任何恐惧条件措施都没有群体差异。这些发现表明,在服用焦虑的焦虑行为和女性中的焦虑性行为中CB1受体信号传导的适度,性别特异性作用。

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