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Identification and cellular localisation of NPW1 (GPR7) receptors for the novel neuropeptide W-23 by [125I]-NPW radioligand binding and immunocytochemistry.

作者信息

Singh Gurminder, Maguire Janet J, Kuc Rhoda E, Fidock Mark, Davenport Anthony P

机构信息

Clinical Pharmacology Unit, Addenbrooke's Hospital, University of Cambridge, Level 6, Centre for Clinical Investigation, Box 110, Cambridge CB2 2QQ, UK.

出版信息

Brain Res. 2004 Aug 13;1017(1-2):222-6. doi: 10.1016/j.brainres.2004.03.079.

Abstract

Using a novel radioligand, we have identified high-affinity binding sites (K(D)=0.44+/-0.13 nM) for the recently discovered peptide, neuropeptide W (NPW), in rat brain. Binding density was highest in the amygdala (B(max)=149.9+/-13.8 fmol/mg protein), thalamic, and hypothalamic nuclei. A similar distribution was observed in mouse brain. We have confirmed the identity of these binding sites as the G-protein-coupled receptor, NPW(1) (previously designated orphan receptor GPR7), using site-directed antisera that revealed receptors were expressed by neuronal cell bodies and processes. Additionally, we have demonstrated the presence of NPW-like immunoreactivity in neuronal cell bodies in areas projecting to the amygdala, such as the dorsal raphe nucleus and ventral tegmental area, providing evidence for an emerging new transmitter system.

摘要

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