...
首页> 外文期刊>Molecular pharmacology. >Functional status of somatodendritic serotonin 1A autoreceptor after long-term treatment with fluoxetine in a mouse model of anxiety/depression based on repeated corticosterone administration
【24h】

Functional status of somatodendritic serotonin 1A autoreceptor after long-term treatment with fluoxetine in a mouse model of anxiety/depression based on repeated corticosterone administration

机译:长期服用氟西汀治疗小鼠焦虑/抑郁模型中的皮质树突状细胞5-羟色胺1A自身受体的功能状态(基于反复服用皮质酮)

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Most preclinical studies investigating the effects and the mechanism of action of antidepressants have been performed in naive rodents. This is inappropriate because antidepressants act on specific symptoms of the pathological condition, such as distress and anxiety. We have developed a mouse model of anxiety/depression based on addition of corticosterone to drinking water. This model is highly reproducible and easy to set up compared with unpredictable chronic mild stress. The serotonin 1A (5-HT 1A) autoreceptor is known to play a role in mood disorders and their treatments. An increase in somatodendritic 5-HT 1Aautoreceptor density in the dorsal raphe (DR) attenuates the therapeutic activity of selective serotonin-reuptake inhibitors (SSRIs), whereas their functional desensitization promotes activation of brain serotonergic transmission, thereby representing an adaptive change relevant to their therapeutic effect. Here we assessed the effects of sustained administration of the SSRI fluoxetine on 5-HT 1A autoreceptor sensitivity in mice administered with corticosterone. Fluoxetine attenuated hypothermia induced by the 5-HT 1A receptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin, decreased DR 5-HT neuronal activity, and decreased 5-HT release in both vehicle- and corticosterone-pretreated mice. However, such desensitization was more pronounced in corticosterone-pretreated mice. This change had an overall effect on serotonergic tone because we found a greater firing rate of 5-HT neurons associated with an enhancement of 5-HT outflow in the DR of corticosterone-pretreated mice in response to fluoxetine compared with the corresponding group of vehicle-pretreated mice. These results provide cellular explanations for the antidepressant effects produced by SSRIs in subjects with pathological conditions but not in naive animals or healthy volunteers.
机译:大多数研究抗抑郁药的作用及其作用机理的临床前研究都是在幼稚的啮齿动物中进行的。这是不适当的,因为抗抑郁药会作用于病理状况的特定症状,例如困扰和焦虑。我们已经开发了基于在饮用水中添加皮质酮的焦虑/抑郁症小鼠模型。与不可预测的慢性轻度压力​​相比,该模型具有很高的可重复性,易于建立。已知血清素1A(5-HT 1A)自体受体在情绪障碍及其治疗中起作用。背脊(DR)中树突状5-HT 1A受体密度的增加减弱了选择性5-羟色胺再摄取抑制剂(SSRI)的治疗活性,而其功能脱敏则促进了脑血清素能传递的激活,从而代表了与其治疗相关的适应性变化影响。在这里,我们评估了持续给予SSRI氟西汀对给予皮质酮的小鼠对5-HT 1A自身受体敏感性的影响。氟西汀减弱了5-HT 1A受体激动剂8-羟基-2-(二-正丙基氨基)四氢萘诱导的体温过低,降低了DR 5-HT神经元活性,并减少了经媒介物和皮质酮治疗的小鼠的5-HT释放。但是,这种脱敏在皮质酮预处理的小鼠中更为明显。这种变化对血清素能的音调产生了总体影响,因为与相应的媒介物组相比,我们发现,在接受氟西汀治疗的皮质类固醇预处理小鼠中,5-HT神经元的激发率更高,与5-HT流出增加有关。预处理的小鼠。这些结果为SSRIs在患有病理性疾病的受试者中产生的抗抑郁作用提供了细胞解释,而在幼稚动物或健康志愿者中则没有。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号