4.5 Article

Hypothalamic alterations in fetuses of high fat diet-fed obese female rats

Journal

JOURNAL OF ENDOCRINOLOGY
Volume 200, Issue 3, Pages 293-300

Publisher

BIOSCIENTIFICA LTD
DOI: 10.1677/JOE-08-0429

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Funding

  1. National Institute of Health grant [DK 061518]

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The offspring of high fat (HF) diet-fed rats display increased body weight during adulthood. However, it is not known whether the changes, in appetite regulation in these animals occur in utero or postnatally. We investigated the effects of maternal obesity induced by a HF: diet prior to and during pregnancy on leptin and insulin signaling and the expression of orexigenic and anorexigenic peptides in term fetal hypothalami. The consumption of a HF diet prior to and during pregnancy resulted in obesity in HF female rats: additionally, HF female rats exhibited hyperinsulinemia and hyperleptinemia which were exaggerated in late gestation by compared with control female rats that Were fed a Standard rodent laboratory chow (LC). Term fetuses of HF female rats (FHF) also had significantly higher serum leptin and insulin levels compared with control fetuses (FLC) while there was no difference in average fetal weight between the two groups. FHF hypothalami showed elevated levels of mRNA and proteins for leptin long receptor and insulin receptor beta-subunit. However, the protein levels of Signal transducers and activators of transcription-3 and insulin receptor substrate-2, the downstream signaling components of leptin and insulin signaling respectively were decreased. Also, FHF hypothalami had increased mRNA levels of neuropeptide Y and agoutirelated polypeptide indicating that orexigenic neuropeptides in HF progeny are already upregulated by term fetal stage. Additionally, the mRNA levels of pro-opiatemelanocortin and melanocortin receptor-4 were also increased in the HF fetal hypothalami. These findings indicate potential programming effects of an altered intrauterine environment induced by HF diet consumption on appetite-regulating neuropeptides, and leptin and insulin signaling in the late fetal period.

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