Annette G. Beck-Sickinger 1, William F. Colmers 2, Helen M. Cox 3, Henri N. Doods 4, Herbert Herzog 5, Dan Larhammar 6, Martin C. Michel 7, Remi Quirion 8, Thue Schwartz 9 and Thomas Westfall 10
Neuropeptide Y (NPY) receptors ( nomenclature as agreed by the NC-IUPHAR Subcommittee on Neuropeptide Y Receptors [ 159 ]) are activated by the endogenous peptides neuropeptide Y , neuropeptide Y-(3-36), peptide YY , PYY-(3-36) and pancreatic polypeptide (PP). The receptor originally identified as the Y3 receptor has been identified as the CXCR4 chemokine recepter (originally named LESTR, [ 140 ]). The y6 receptor is a functional gene product in mouse, absent in rat, but contains a frame-shift mutation in primates producing a truncated non-functional gene [ 85 ]. Three-dimensional structures have been determined for subtype active receptors Y 1, Y 2 and Y 4 [216 , 115 ] and inactive antagonist bound Y 1 and Y 2 receptors [ 245 , 215 ]. Many of the agonists exhibit differing degrees of selectivity dependent on the species examined. For example, the potency of PP is greater at the rat Y 4 receptor than at the human receptor [ 63 ]. In addition, many agonists lack selectivity for individual subtypes, but can exhibit comparable potency against pairs of NPY receptor subtypes, or have not been examined for activity at all subtypes. [ 125 I]-PYY or [ 125 I]-NPY can be used to label Y 1, Y 2, Y 5 and y 6 subtypes non-selectively, while [125 I][cPP(1-7), NPY(19-23), Ala 31 , Aib 32 , Gln 34 ]hPP may be used to label Y 5 receptors preferentially (note that cPP denotes chicken peptide sequence and hPP is the human sequence).
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Y1 receptor
Y2 receptor
Y4 receptor
Y5 receptor
y6 receptor