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Role of premature leptin surge in obesity resulting from intrauterine undernutrition.

Authors
  • Yura, Shigeo
  • Itoh, Hiroaki
  • Sagawa, Norimasa
  • Yamamoto, Hiroshi
  • Masuzaki, Hiroaki
  • Nakao, Kazuwa
  • Kawamura, Makoto
  • Takemura, Maki
  • Kakui, Kazuyo
  • Ogawa, Yoshihiro
  • Fujii, Shingo
Type
Published Article
Journal
Cell Metabolism
Publisher
Elsevier
Publication Date
Jun 01, 2005
Volume
1
Issue
6
Pages
371–378
Identifiers
PMID: 16054086
Source
Medline
License
Unknown

Abstract

Intrauterine undernutrition is closely associated with obesity related to detrimental metabolic sequelae in adulthood. We report a mouse model in which offspring with fetal undernutrition (UN offspring), when fed a high-fat diet (HFD), develop pronounced weight gain and adiposity. In the neonatal period, UN offspring exhibited a premature onset of neonatal leptin surge compared to offspring with intrauterine normal nutrition (NN offspring). Unexpectedly, premature leptin surge generated in NN offspring by exogenous leptin administration led to accelerated weight gain with an HFD. Both UN offspring and neonatally leptin-treated NN offspring exhibited an impaired response to acute peripheral leptin administration on a regular chow diet (RCD) with impaired leptin transport to the brain as well as an increased density of hypothalamic nerve terminals. The present study suggests that the premature leptin surge alters energy regulation by the hypothalamus and contributes to "developmental origins of health and disease."

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