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Effects of intrauterine undernutrition on hypothalamic Kiss1 expression and the timing of puberty in female rats.

机译:宫内营养不足对雌性大鼠下丘脑Kiss1表达及青春期时机的影响。

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Recent studies have suggested that intrauterine undernutrition is closely associated with the pathogenesis of diseases after birth. Perinatal undernutrition is known to disturb the development of reproductive function and delay the onset of puberty in some species. Using a rat model, we determined the effects of prenatal undernutrition on the development of the hypothalamic kisspeptin system and evaluated whether the alteration of the kisspeptin system contributes to the delayed onset of puberty induced by prenatal undernutrition. We also evaluated the effects of prenatal undernutrition on the developmental changes in serum leptin levels because leptin was a putative positive regulator of the hypothalamic kisspeptin system. We compared the timing of vaginal opening (VO) and the developmental changes in body weight, hypothalamic Kiss1 mRNA levels, and serum leptin concentrations between offspring with prenatal undernutrition (UN offspring) and normal nutrition (NN offspring). After birth, the UN offspring showed rapid growth and had caught up to body weight of the NN offspring by postnatal day 12. After postnatal day 16, the UN offspring showed significantly lower Kiss1 mRNA levels than the NN offspring, despite their significantly higher serum leptin levels (at days 20 and 28). The timing of VO in the UN offspring was delayed compared with that in the NN offspring, and chronic central injection of kisspeptin normalized the timing of VO in the UN offspring. These results suggest that decreased hypothalamic kisspeptin action contributes to the delayed onset of puberty in prenatally undernourished female rats. Increased leptin resistance in the kisspeptin system might be involved in these alterations.
机译:最近的研究表明,宫内营养不良与出生后疾病的发病机理密切相关。众所周知,围产期营养不良会干扰某些物种的生殖功能,并延缓青春期的发作。使用大鼠模型,我们确定了产前营养不足对下丘脑kisepteptin系统发育的影响,并评估了kisepteptin系统的改变是否有助于由产前营养不足引起的青春期延迟发作。我们还评估了产前营养不良对血清瘦素水平发展变化的影响,因为瘦素是下丘脑吻合肽系统的一种假定的正调节剂。我们比较了带营养不良的后代(UN后代)和正常营养(NN后代)之间的阴道开放时间(VO)以及体重,下丘脑Kiss1 mRNA水平和血清瘦素浓度的发育变化。出生后,联合国后代表现出快速的成长,并在出生后第12天达到了NN后代的体重。出生后第16天,联合国后代显示出比NN后代明显低的Kiss1 mRNA水平,尽管他们的血清瘦素明显更高。水平(第20和28天)。与NN后代相比,联合国后代的VO时机延迟了,而长期集中注射kisepteptin使联合国后代的VO时机正常化。这些结果表明,下丘脑kisepteptin的作用降低导致出生前营养不良的雌性大鼠青春期延迟发作。在kisseptin系统中,瘦素抵抗力增强可能与这些改变有关。

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