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在小鼠中,κ 阿片受体刺激或急性应激后,大脑区域特异性 c-Fos 激活的性别差异。

Sex Differences in Brain Region-Specific Activation of c-Fos following Kappa Opioid Receptor Stimulation or Acute Stress in Mice.

机构信息

Department of Life Sciences, University of Bath, Bath BA2 7AY, UK.

出版信息

Int J Mol Sci. 2023 Oct 11;24(20):15098. doi: 10.3390/ijms242015098.

DOI:10.3390/ijms242015098
PMID:37894779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10606335/
Abstract

Kappa opioid receptors (KOPr) are involved in the response to stress. KOPr are also targets for the treatment of stress-related psychiatric disorders including depression, anxiety, and addiction although effects of KOPr are often sex-dependent. Here we investigated c-Fos expression in a range of brain regions in male and female mice following an acute stressor, and a single injection of KOPr agonist. Using adult C57BL/6 c-Fos-GFP transgenic mice and quantitative fluorescence microscopy, we identified brain regions activated in response to a challenge with the KOPr agonist U50,488 (20 mg/kg) or an acute stress (15 min forced swim stress, FSS). In male mice, U50,488 increased expression of c-Fos in the prelimbic area of the prefrontal cortex (PFCx), nucleus accumbens (NAcc), and basolateral nuclei of the amygdala (BLA). In contrast, in female mice U50,488 only activated the BLA but not the PFCx or the NAcc. FSS increased activation of PFCx, NAcc, and BLA in males while there was no activation of the PFCx in female mice. In both sexes, the KOPr antagonist norBNI significantly blocked U50,488-induced, but not stress-induced activation of brain regions. In separate experiments, activated cells were confirmed as non-GABAergic neurons in the PFCx and NAcc. Together these data demonstrate sex differences in activation of brain regions that are key components of the 'reward' circuitry. These differential responses may contribute to sex differences in stress-related psychiatric disorders and in the treatment of depression, anxiety, and addiction.

摘要

κ 阿片受体(KOPr)参与应激反应。KOPr 也是治疗与应激相关的精神疾病(包括抑郁症、焦虑症和成瘾)的靶点,尽管 KOPr 的作用通常具有性别依赖性。在这里,我们研究了急性应激源和单次 KOPr 激动剂注射后雄性和雌性小鼠一系列脑区的 c-Fos 表达。使用成年 C57BL/6 c-Fos-GFP 转基因小鼠和定量荧光显微镜,我们确定了对 KOPr 激动剂 U50,488(20mg/kg)或急性应激(15min 强迫游泳应激,FSS)挑战有反应的脑区。在雄性小鼠中,U50,488 增加了前额叶皮层(PFCx)、伏隔核(NAcc)和杏仁核基底外侧核(BLA)的 c-Fos 表达。相比之下,在雌性小鼠中,U50,488 仅激活了 BLA,而不激活 PFCx 或 NAcc。FSS 增加了雄性小鼠的 PFCx、NAcc 和 BLA 的激活,而雌性小鼠的 PFCx 没有激活。在两性中,KOPr 拮抗剂 norBNI 显著阻断了 U50,488 诱导的、但不是应激诱导的脑区激活。在单独的实验中,激活的细胞被确认为 PFCx 和 NAcc 中的非 GABA 能神经元。总之,这些数据表明,在激活大脑区域方面存在性别差异,这些区域是“奖励”回路的关键组成部分。这些差异反应可能有助于应激相关精神疾病以及抑郁症、焦虑症和成瘾的治疗中的性别差异。

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