Chronic administration of neuropeptide Y into the lateral ventricle of C57BL/6J male mice produces an obesity syndrome including hyperphagia, hyperleptinemia, insulin resistance, and hypogonadism

Mol Cell Endocrinol. 2001 Dec 20;185(1-2):195-204. doi: 10.1016/s0303-7207(01)00620-7.


Neuropeptide Y (NPY) is involved in the central regulation of appetite, sexual behavior, and reproductive function. We have previously shown that chronic infusion of NPY into the lateral ventricle of normal rats produced an obesity syndrome characterized by hyperphagia, hyperinsulinism and collapse of reproductive function. We further demonstrated that acute inhibition of LH secretion in castrated rats was preferentially mediated by the NPY receptor subtype 5 (Y(5)). In the present study, the effects of chronic, central infusion of NPY, or the mixed Y2-Y5 agonist PYY(3-36), were evaluated both in normal male C57BL/6J mice and Sprague-Dawley rats. After a 7-day infusion to male mice, both NPY and PYY(3-36) at 5 nmol per day, induced marked hyperphagia leading to significant increases in body and fat pad weights. Furthermore, both compounds markedly reduced several markers of the reproductive axis. In the rat study, PYY(3-36) was more active than NPY to inhibit the pituitary-testicular axis, confirming the importance of the Y5 subtype for such effects. In the mouse, chronic NPY infusion induced a sustained increase in corticosterone and insulin secretion. Plasma leptin levels were also markedly increased possibly explaining the observed reduction in gene expression for hypothalamic NPY. Gene expression for hypothalamic POMC was reduced in the NPY- or PYY(3-36)-infused mice, suggesting that NPY exacerbated food intake by both acting through its own receptor(s), and reducing the satiety signal driven by the POMC-derived alpha-MSH. The present study in the mouse suggests in analogy with available rat data, that constant exposure to elevated NPY in the hypothalamic area unabatedly enhances food intake leading to an obesity syndrome including increased adiposity, insulin resistance, hypercorticism, and hypogonadism, reminiscent of the phenotype of the ob/ob mouse, that displays elevated hypothalamic NPY secondary to lack of leptin negative feedback action.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Hyperphagia / chemically induced
  • Hyperphagia / etiology
  • Hypogonadism / chemically induced
  • Hypogonadism / etiology
  • Insulin Resistance
  • Lateral Ventricles
  • Leptin / blood
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neuropeptide Y / administration & dosage
  • Neuropeptide Y / pharmacology*
  • Obesity / chemically induced*
  • Obesity / etiology
  • Obesity / pathology
  • Peptide Fragments
  • Peptide YY / administration & dosage
  • Peptide YY / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Syndrome


  • Leptin
  • Neuropeptide Y
  • Peptide Fragments
  • Peptide YY
  • peptide YY (3-36)