Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6261710 | Brain Research Bulletin | 2015 | 7 Pages |
â¢QRFP-26 was microinjected into the medial hypothalamic area of male Wistar rats.â¢100 ng and 200 ng doses of QRFP-26 increased liquid food intake.â¢Effective doses of QRFP-26 did not affect general locomotor activity in open field.â¢Pretreatment with receptor antagonist BIBP3226 prevented QRFP-26 effects on feeding.
The RFamide peptide family comprises a number of biologically active peptides sharing RF motif at their C-terminal end. These peptides are involved in the control of multiple physiological functions including regulation of metabolism and feeding behavior. QRFP-43 as well as its 26-aminoacid residue QRFP-26 are able to cause orexigenic effect when administered to the rodents' cerebral ventricles. QRFPs have been suggested as the endogenous ligands of the previously orphan GPR103 receptors. GPR103 receptors share amino acid identity with other receptors of neuropeptides involved in feeding (NPY, NPFF, galanin). QRFP-26 expressing neurons and binding sites are densely present in the rat medial hypothalamus (MHA), an area directly responsible for the regulation of feeding. QRFP-26 was delivered to the target area by direct intrahypothalamic microinjection, and the consumption of liquid food was measured over a 60Â min period. Both doses (100 and 200Â ng) significantly increased food intake. Non-specific receptor antagonist BIBP3226 eliminated the orexigenic effect caused by QRFP-26 administration. Effective doses of QRFP-26 did not modify general locomotor activity and behavioral patterns examined in the open-field test. This study is the first reporting feeding modulating effects following direct intrahypothalamic QRFP-26 administration.