Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 2009 Nov;158(Suppl 1):S75. doi: 10.1111/j.1476-5381.2009.00501_46.x

Neuropeptides B and W

PMCID: PMC2884623

Overview: The neuropeptide BW receptor 1 (NPBW1, provisional nomenclature) is activated by two 23-amino-acid peptides, neuropeptide W (NPW-23) and neuropeptide B (NPB-23) (Shimomura et al., 2002; Fujii et al., 2002). C-terminally extended forms of the peptides (NPW-30 and NPB-29) also activate NPBW1 (Brezillon et al., 2003). Unique to both forms of NPB is the N-terminal bromination of the first tryptophan residue. des-Br-NPB-23 and des-Br-NPB-29 were not found to be major components of bovine hypothalamic tissue extracts. The NPBW2 receptor is activated by the short and C-terminal extended forms of NPB and NPW (Brezillon et al., 2003).

Nomenclature NPBW1 NPBW2
Other names GPR7 GPR8
Ensembl ID ENSG00000183729 ENSG00000125522
Principal transduction Gi/0 (Mazzocchi et al., 2005) Gi/0 (Mazzocchi et al., 2005)
Rank order of potency NPB-29 > NPB-23 > NPW-23 > NPW-30 (Brezillon et al., 2003) NPW-23 > NPW-30 > NPB-29 > NPB-23 (Brezillon et al., 2003)
Selective agonists Ava-3, Ava-5 (Kanesaka et al., 2007)
Probes >[125I]-NPW-23 (0.44 nM, Singh et al., 2004) [125I]-NPW-23

Potency measurements were conducted with heterologously expressed receptors with a range of 0.14–0.57 nM (NPBW1) and 0.98–21 nM (NPBW2).

Glossary

Abbreviations:

Ava3

TrpTyrLysAvaAvaAvaGlyArgAlaAlaGlyLeuLeuSerGlyLeu-NH2

Ava5

TrpTyrLysAvaAvaAvaAvaAvaAvaGlyArgAlaAlaGlyLeuLeuSerGlyLeu-NH2

Further Reading

Lee DK, George SR, O'Dowd BF (2003). Continued discovery of ligands for G protein-coupled receptors. Life Sci74: 293–297.

Singh G, Davenport AP (2006). Neuropeptide B and W: neurotransmitters in an emerging G-protein-coupled receptor system. Br J Pharmacol148: 1033–1041.

References

  1. Brezillon S, et al. J Biol Chem. 2003;278:776–783. doi: 10.1074/jbc.M206396200. [DOI] [PubMed] [Google Scholar]
  2. Fujii R, et al. J Biol Chem. 2002;277:34010–34016. doi: 10.1074/jbc.M205883200. [DOI] [PubMed] [Google Scholar]
  3. Kanesaka M, et al. J Peptide Sci. 2007;13:379–385. doi: 10.1002/psc.855. [DOI] [PubMed] [Google Scholar]
  4. Mazzocchi G, et al. J Clin Endocrinol Metab. 2005;90:3466–3471. doi: 10.1210/jc.2004-2132. [DOI] [PubMed] [Google Scholar]
  5. Shimomura Y, et al. J Biol Chem. 2002;277:35826–35832. doi: 10.1074/jbc.M205337200. [DOI] [PubMed] [Google Scholar]
  6. Singh G, et al. Brain Res. 2004;1017:222–226. doi: 10.1016/j.brainres.2004.03.079. [DOI] [PubMed] [Google Scholar]
  7. Singh G, Davenport AP. Br J Pharmacol. 2006;148:1033–1041. doi: 10.1038/sj.bjp.0706825. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES