首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Involvement of median raphe nucleus 5-HT1A receptors in the regulation of generalized anxiety-related defensive behaviours in rats.
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Involvement of median raphe nucleus 5-HT1A receptors in the regulation of generalized anxiety-related defensive behaviours in rats.

机译:中位数缝核5-HT1A受体参与大鼠广泛性焦虑相关防御行为的调节。

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Changes in 5-HT1A receptor-mediated neurotransmission at the level of the median raphe nucleus (MRN) are reported to affect the expression of defensive responses that are associated with generalized anxiety disorder (e.g. inhibitory avoidance) but not with panic (e.g. escape). The objective of this study was to further explore the involvement of MRN 5-HT1A receptors in the regulation of generalized anxiety-related behaviours. Results of experiment 1 showed that intra-MRN injection of the 5-HT1A/7 receptor agonist 8-OH-DPAT (0.6 nmol) in male Wistar rats impaired the acquisition of inhibitory avoidance, without interfering with the performance of escape in the elevated T-maze test of anxiety. Pre-treatment with the 5-HT1A receptor antagonist WAY-100635 (0.18 nmol) fully blocked this anxiolytic-like effect. As revealed by experiment 2, intra-MRN injection of 8-OH-DPAT (0.6, 3 or 15 nmol) also caused anxiolytic effect in rats submitted to the light-dark transition test, another animal model that has been associated with generalized anxiety. In the same test, intra-MRN injection of WAY-100635 (0.18, 0.37 or 0.74 nmol) caused the opposite effect. Overall, the current findings support the view that MRN 5-HT neurons, through the regulation of 5-HT1A somatodendritic autoreceptors, are implicated in the regulation of generalized anxiety-associated behaviours.
机译:据报道,在中位数缝核(MRN)水平上5-HT1A受体介导的神经传递的变化会影响与广泛性焦虑症(例如抑制回避)相关的防御反应的表达,但与恐慌(例如逃避)无关。这项研究的目的是进一步探索MRN 5-HT1A受体参与广泛性焦虑相关行为的调节。实验1的结果表明,在雄性Wistar大鼠中,MRN内注射5-HT1A / 7受体激动剂8-OH-DPAT(0.6 nmol)会损害抑制性规避的获得,而不会干扰T升高时的逃避性能。 -迷宫测试焦虑。用5-HT1A受体拮抗剂WAY-100635(0.18 nmol)进行的预处理完全阻断了这种抗焦虑作用。正如实验2所揭示的,MRN内注射8-OH-DPAT(0.6、3或15 nmol)也引起了接受明暗转换试验的大鼠的抗焦虑作用,这是另一种与广泛性焦虑相关的动物模型。在同一测试中,MRN内注射WAY-100635(0.18、0.37或0.74 nmol)产生相反的效果。总的来说,当前的发现支持这样的观点,即MRN 5-HT神经元通过调节5-HT1A体树突状自体受体,参与了与广泛性焦虑相关的行为的调节。

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