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新生大鼠瘦素信号通路的阻断会诱发下丘脑的变化,这些变化与青春期启动延迟以及成年期神经肽表达的改变有关。

Blockage of neonatal leptin signaling induces changes in the hypothalamus associated with delayed pubertal onset and modifications in neuropeptide expression during adulthood in male rats.

作者信息

Mela Virginia, Jimenez Sara, Freire-Regatillo Alejandra, Barrios Vicente, Marco Eva-María, Lopez-Rodriguez Ana-Belén, Argente Jesús, Viveros María-Paz, Chowen Julie A

机构信息

Department of Physiology (Animal Physiology II), Faculty of Biology, Universidad Complutense, Madrid, Spain.

Department of Endocrinology, Hospital Infantil Universitario Niño Jesús, Instituto de Investigación Sanitaria Princesa (IP), Madrid, Spain; Department of Pediatrics, Universidad Autónoma de Madrid, Madrid, Spain; CIBER Fisiopatología de Obesidad y Nutrición, Instituto Carlos III, Madrid, Spain.

出版信息

Peptides. 2016 Dec;86:63-71. doi: 10.1016/j.peptides.2016.10.003. Epub 2016 Oct 14.

Abstract

The neonatal leptin surge, occurring from postnatal day (PND) 5 to 13 and peaking at PND9 in rodents, is important for the development of neuroendocrine circuits involved in metabolic control and reproductive function. We previously demonstrated that treatment with a leptin antagonist from PND 5 to 9, coincident with peak leptin levels in the neonatal surge, modified trophic factors and markers of cell turnover and neuronal maturation in the hypothalamus of peri-pubertal rats. The kisspeptin system and metabolic neuropeptide and hormone levels were also modified. Here our aim was to investigate if the timing of pubertal onset is altered by neonatal leptin antagonism and if the previously observed peripubertal modifications in hormones and neuropeptides persist into adulthood and affect male sexual behavior. To this end, male Wistar rats were treated with a pegylated super leptin antagonist (5mg/kg, s.c.) from PND 5 to 9 and killed at PND102-103. The appearance of external signs of pubertal onset was delayed. Hypothalamic kiss1 mRNA levels were decreased in adult animals, but sexual behavior was not significantly modified. Although there was no effect on body weight or food intake, circulating leptin, insulin and triglyceride levels were increased, while hypothalamic leptin receptor, POMC and AgRP mRNA levels were decreased. In conclusion, alteration of the neonatal leptin surge can modify the timing of pubertal onset and have long-term effects on hypothalamic expression of reproductive and metabolic neuropeptides.

摘要

新生期瘦素激增发生在出生后第5天至13天,在啮齿动物中于出生后第9天达到峰值,这对于参与代谢控制和生殖功能的神经内分泌回路的发育很重要。我们之前证明,从出生后第5天至第9天用瘦素拮抗剂进行治疗,这与新生期激增时的瘦素峰值一致,可改变青春期前大鼠下丘脑的营养因子、细胞更新标志物和神经元成熟情况。亲吻素系统以及代谢神经肽和激素水平也发生了改变。在此,我们的目的是研究新生期瘦素拮抗作用是否会改变青春期启动的时间,以及之前观察到的青春期前激素和神经肽的改变是否会持续到成年并影响雄性性行为。为此,从出生后第5天至第9天,对雄性Wistar大鼠皮下注射聚乙二醇化超级瘦素拮抗剂(5mg/kg),并在出生后第102 - 103天处死。青春期启动外部体征的出现延迟。成年动物下丘脑kiss1 mRNA水平降低,但性行为没有明显改变。虽然对体重或食物摄入量没有影响,但循环中的瘦素、胰岛素和甘油三酯水平升高,而下丘脑瘦素受体、POMC和AgRP mRNA水平降低。总之,新生期瘦素激增的改变可改变青春期启动的时间,并对生殖和代谢神经肽的下丘脑表达产生长期影响。

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