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Characterization of Y 3 receptor‐mediated synaptic inhibition by chimeric neuropeptide Y‐peptide YY peptides in the rat brainstem
Author(s) -
Glaum Steven R.,
Miller Richard J.,
Rhim Hyewhon,
Maclean Derek,
Georgic Ynn M.,
MacKenzie Robert G.,
Grundemar Lars
Publication year - 1997
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0700883
Subject(s) - peptide yy , neuropeptide y receptor , medicine , endocrinology , chemistry , receptor , inhibitory postsynaptic potential , neuropeptide , biology
1 Neuropeptide Y (NPY) and peptide YY (PYY) act at receptors referred to as Y 1 and Y 2 , while the Y 3 receptor is specific to NPY and does not recognize PYY. The effects of NPY, its related peptides and a series of newly constructed chimeric NPY‐PYY peptides were examined on excitatory and inhibitory postsynaptic currents (e.p.s.cs and i.p.s.cs, respectively) in rat dorsomedial nucleus tractus solitarius (NTS) neurones recorded in coronal brainstem slices. Monosynaptic activity was evoked by electrical stimulation in the region of the tractus solitarius. 2 NPY (5–500 nM) inhibited e.p.s.cs and i.p.s.cs in a concentration‐dependent manner. In contrast, PYY (500 nM) failed to affect either e.p.s.cs or i.p.s.cs. The N‐and C‐terminal parts of a series of chimeric NPY‐PYY peptides were joined at positions where NPY and PYY sequences differ. In binding experiments the chimeric peptides were all about equipotent with NPY and PYY in displacing [ 125 I]‐PYY from Y 1 and Y 2 binding sites on SK‐N‐MC cells and rat hippocampus respectively. 3 In the whole cell voltage clamp recordings of NTS neurones, NPY(1‐23)‐PYY(24–36) and NPY(1‐14)‐PYY(15–36) evoked a concentration‐dependent inhibition of e.p.s.cs and i.p.s.cs, while NPY(l‐7)‐PYY(8–36) and NPY(1‐3)‐PYY(4–36) were inactive. The only differences in amino acid residues between NPY(l‐14)‐PYY(15–36) and NPY(1‐7)‐PYY(8–36) reside in positions 13 and 14. 4 Furthermore, [Pro 34 ]NPY (500 nM) was equivalent in potency to NPY itself at inhibiting monosynaptic transmission in NTS, while [Leu 31 ,Pro 34 ]NPY and pancreatic polypeptide (both at 500 nM) failed to affect synaptic transmission. 5 The present study has shown that NPY acts at Y 3 receptors to suppress both excitatory and inhibitory currents in the NTS. The different efficacy of the chimeric NPY‐PYY peptides suggests that positions 13 and 14 are of great importance for Y 3 receptor recognition. Finally, this receptor type readily recognizes [Pro 34 ]NPY, but not [Leu 31 ,Pro 34 ]NPY.