Max Planck Institute of Psychiatry, Munich, Germany.
Neuropsychopharmacology. 2012 May;37(6):1323-37. doi: 10.1038/npp.2011.317. Epub 2012 Jan 25.
Experiments in rodents revealed neuropeptide S (NPS) to constitute a potential novel treatment option for anxiety diseases such as panic and post-traumatic stress disorder. However, both its cerebral target sites and the molecular underpinnings of NPS-mediated effects still remain elusive. By administration of fluorophore-conjugated NPS, we pinpointed NPS target neurons in distinct regions throughout the entire brain. We demonstrated their functional relevance in the hippocampus. In the CA1 region, NPS modulates synaptic transmission and plasticity. NPS is taken up into NPS receptor-expressing neurons by internalization of the receptor-ligand complex as we confirmed by subsequent cell culture studies. Furthermore, we tracked internalization of intranasally applied NPS at the single-neuron level and additionally demonstrate that it is delivered into the mouse brain without losing its anxiolytic properties. Finally, we show that NPS differentially modulates the expression of proteins of the glutamatergic system involved inter alia in synaptic plasticity. These results not only enlighten the path of NPS in the brain, but also establish a non-invasive method for NPS administration in mice, thus strongly encouraging translation into a novel therapeutic approach for pathological anxiety in humans.
在啮齿类动物实验中发现,神经肽 S(NPS)可能成为治疗焦虑症(如恐慌症和创伤后应激障碍)的新方法。然而,其脑内靶标和 NPS 介导作用的分子基础仍然难以捉摸。通过给予荧光标记的 NPS,我们确定了整个大脑中不同区域 NPS 的靶神经元。我们在海马体中证明了它们的功能相关性。在 CA1 区域,NPS 调节突触传递和可塑性。我们通过后续的细胞培养研究证实,NPS 通过受体-配体复合物的内化被摄取到表达 NPS 受体的神经元中。此外,我们在单细胞水平上追踪了经鼻内给予的 NPS 的内化,并进一步证明它可以进入小鼠大脑而不会失去其抗焦虑特性。最后,我们表明 NPS 可调节谷氨酸能系统蛋白的表达,这些蛋白参与突触可塑性等过程。这些结果不仅阐明了 NPS 在大脑中的途径,还建立了一种在小鼠中给予 NPS 的非侵入性方法,因此强烈鼓励将其转化为治疗病理性焦虑的新方法。