Enhanced food intake by progesterone-treated female rats is related to changes in neuropeptide genes expression in hypothalamus

被引:14
作者
Stelmanska, Ewa [1 ]
Sucajtys-Szulc, Elzbieta [2 ]
机构
[1] Med Univ Gdansk, Dept Biochem, PL-80211 Gdansk, Poland
[2] Med Univ Gdansk, Dept Nephrol Transplantol & Internal Med, PL-80211 Gdansk, Poland
关键词
progesterone; cocaine and amphetamine regulated transcript (CART); neuropeptide Y (NPY); progesterone receptor (PR); LUTEINIZING-HORMONE; MEGESTROL-ACETATE; OVARIAN HORMONES; MESSENGER-RNA; UP-REGULATION; BODY-WEIGHT; LEPTIN; RESTRICTION; NPY; PREGNANCY;
D O I
10.5603/EP.2014.0007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Progesterone-treated females eat more food, but the mechanism underlying this effect is not well understood. The aim of the study was to analyse the effect of progesterone on neuropeptide genes expression in rat hypothalamus. Material and methods: Experiments were carried out on female and male Wistar rats. Animals were treated with progesterone (100 mg per rat) for 28 days. NPY and CART mRNA levels in hypothalamus were quantified by real-time PCR. The serum progesterone concentration was determined by radioimmunoassay. Results: Progesterone administration to females caused an increase in food intake, body mass, and white adipose tissue mass. Elevated circulating progesterone concentration up-regulated NPY and down-regulated CART genes expression in hypothalamus of females. In males, elevated blood progesterone concentration had no effect on food intake, body and fat mass and on the neuropeptide genes expression in hypothalamus. Moreover, administration of progesterone in females resulted in decrease of PR mRNA level in hypothalamus. No effect of progesterone administration on PR mRNA level in hypothalamus of males was found. Conclusions: The changes in neuropeptide genes expression in hypothalamus may lead to stimulation of appetite and might explain the observed increase in food intake, body and adipose tissue mass in progesterone-treated females.
引用
收藏
页码:46 / 52
页数:7
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