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Post-weaning high-fat diet accelerates kidney injury, but not hypertension programmed by maternal diabetes.
Aliou, Yessoufou; Liao, Min-Chun; Zhao, Xin-Ping; Chang, Shiao-Ying; Chenier, Isabelle; Ingelfinger, Julie R; Zhang, Shao-Ling.
Afiliação
  • Aliou Y; Centre de recherche du Centre hospitalier de l'Universite de Montreal (CRCHUM), Universite de Montreal, Montréal, Quebec, Canada.
  • Liao MC; Centre de recherche du Centre hospitalier de l'Universite de Montreal (CRCHUM), Universite de Montreal, Montréal, Quebec, Canada.
  • Zhao XP; Centre de recherche du Centre hospitalier de l'Universite de Montreal (CRCHUM), Universite de Montreal, Montréal, Quebec, Canada.
  • Chang SY; Centre de recherche du Centre hospitalier de l'Universite de Montreal (CRCHUM), Universite de Montreal, Montréal, Quebec, Canada.
  • Chenier I; Centre de recherche du Centre hospitalier de l'Universite de Montreal (CRCHUM), Universite de Montreal, Montréal, Quebec, Canada.
  • Ingelfinger JR; Pediatric Nephrology Unit, Massachusetts General Hospital and Harvard Medical School Boston, Boston, Massachusetts.
  • Zhang SL; Centre de recherche du Centre hospitalier de l'Universite de Montreal (CRCHUM), Universite de Montreal, Montréal, Quebec, Canada.
Pediatr Res ; 79(3): 416-24, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26571223
ABSTRACT

BACKGROUND:

The aim of this study was to establish the underlying mechanisms by which a post-weaning high-fat diet (HFD) accelerates the perinatal programming of kidney injury occurring in the offspring of diabetic mothers.

METHODS:

Male mice, offspring of nondiabetic and diabetic dams were fed with normal diet (ND) or HFD from 4 to 20 wk of age. Rat renal proximal tubular cells were used in vitro.

RESULTS:

On ND, the offspring of dams with severe maternal diabetes had an intrauterine growth restriction (IUGR) phenotype and developed mild hypertension and evidence of kidney injury in adulthood. Exposing the IUGR offspring to HFD resulted in rapid weight gain, catch-up growth, and later to profound kidney injury with activation of renal TGFß1 and collagen type IV expression, increased oxidative stress, and enhanced renal lipid deposition, but not systemic hypertension. Given our data, we speculate that HFD or free fatty acids may accelerate the process of perinatal programming of kidney injury, via increased CD36 and fatty acid-binding protein 4 expression, which may target reactive oxygen species, nuclear factor-kappa B, and TGFß1 signaling in vivo and in vitro.

CONCLUSION:

Early postnatal exposure to overnutrition with a HFD increases the risk of development of kidney injury, but not hypertension, in IUGR offspring of dams with maternal diabetes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Gestacional / Dieta Hiperlipídica / Hipertensão / Rim Limite: Animals / Pregnancy Idioma: En Revista: Pediatr Res Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Gestacional / Dieta Hiperlipídica / Hipertensão / Rim Limite: Animals / Pregnancy Idioma: En Revista: Pediatr Res Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá