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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1995 Sep 26;92(20):9067–9071. doi: 10.1073/pnas.92.20.9067

High-affinity neuropeptide Y receptor antagonists.

A J Daniels 1, J E Matthews 1, R J Slepetis 1, M Jansen 1, O H Viveros 1, A Tadepalli 1, W Harrington 1, D Heyer 1, A Landavazo 1, J J Leban 1, et al.
PMCID: PMC40925  PMID: 7568074

Abstract

Neuropeptide Y (NPY) is one of the most abundant peptide transmitters in the mammalian brain. In the periphery it is costored and coreleased with norepinephrine from sympathetic nerve terminals. However, the physiological functions of this peptide remain unclear because of the absence of specific high-affinity receptor antagonists. Three potent NPY receptor antagonists were synthesized and tested for their biological activity in in vitro, ex vivo, and in vivo functional assays. We describe here the effects of these antagonists inhibiting specific radiolabeled NPY binding at Y1 and Y2 receptors and antagonizing the effects of NPY in human erythroleukemia cell intracellular calcium mobilization perfusion pressure in the isolated rat kidney, and mean arterial blood pressure in anesthetized rats.

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Selected References

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