Open AccessThe anorexic hormone Peptide YY 3–36 is rapidly metabolized to inactive Peptide YY 3–34 in vivo
Author(s) -
Toräng Signe,
Veedfald Simon,
Rosenkilde Mette Marie,
Hartmann Bolette,
Holst Jens Juul
Publication year - 2015
Publication title -
physiological reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 39
ISSN - 2051-817X
DOI - 10.14814/phy2.12455
Subject(s) - peptide yy , metabolite , endocrinology , medicine , pancreatic polypeptide , chemistry , peptide , enteroendocrine cell , neuropeptide y receptor , receptor , radioimmunoassay , hormone , biology , neuropeptide , biochemistry , endocrine system , glucagon
Abstract Peptide YY ( PYY ) is a 36 amino acid peptide hormone released from enteroendocrine cells. An N‐terminally degraded metabolite, PYY 3–36, has anorexigenic effects, which makes the PYY system a target for obesity treatment. However, little is known about the kinetics and degradation products of PYY . A related peptide, Neuropeptide Y ( NPY ), may be degraded from the C‐terminus. We therefore investigated PYY degradation after in vitro incubations in porcine plasma and blood and in vivo by infusing PYY 3–36 into multicatheterized pigs ( n = 7) (2 pmol/kg/min). Plasma samples were analyzed by region‐specific radioimmunoassays ( RIA ) and HPLC analysis. A metabolite, corresponding to PYY 3–34 was formed after incubation in plasma and blood and during the infusion study. When taking the C‐terminal degradation into account, the half‐life ( T ½) of PYY in blood and plasma amounted to 3.4 ± 0.2 and 6.2 ± 0.2 h, respectively. After PYY 3–36 infusion in pigs, the peptide was degraded with a T ½ of 3.6 ± 0.5 min. Significant extraction (20.5 ± 8.0%) compatible with glomerular filtration was observed across the kidneys and significant C‐terminal degradation (26.5 ± 4.8%) was observed across the liver. Net balances across the hind limb, splanchnic bed, and lungs were not significantly different from zero. PYY 3–34 was unable to activate the Y2 receptor in a transfected cell line. In conclusion, PYY 3–36 is extensively degraded to PYY 3–34 in the pig, a degradation that renders the peptide inactive on the Y2 receptor. Currently used assays are unlikely to be able to detect this degradation and therefore measure falsely elevated levels of PYY 3–36 , leading to underestimation of its physiological effects.