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首页> 外文期刊>Reproductive toxicology >Prior attenuation of KiSS1/GPR54 signaling in the anteroventral periventricular nucleus is a trigger for the delayed effect induced by neonatal exposure to 17alpha-ethynylestradiol in female rats
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Prior attenuation of KiSS1/GPR54 signaling in the anteroventral periventricular nucleus is a trigger for the delayed effect induced by neonatal exposure to 17alpha-ethynylestradiol in female rats

机译:KiSS1 / GPR54信号在前室室周围核中的先前衰减是雌性大鼠新生暴露于17α-乙炔雌二醇诱导的延迟效应的触发因素

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摘要

Neonatal exposure to 17alpha-ethynylestradiol (EE) causes delayed effect, a late-occurring irreversible damage to reproductive functions characterized by the early onset of age-matched abnormal estrous cycling. To clarify the involvement of a hypothalamic key cycling regulator KiSS1/GPR54 in the delayed effect, we investigated artificially induced LH surges and KiSS1 mRNA expression in the anteroventral periventricular nucleus (AVPV) of cycling young adult rats neonatally exposed to EE, and compared these parameters to those in about 5 months old middle-aged rats. KiSS1 mRNA expression, the number of KiSS1-positive cells and KiSS1/ER alpha co-expressing cells in the AVPV decreased in both EE-exposed and middle-aged rats. The peak area and levels of LH surge dose-dependently decreased in EE-exposed rats, and reduction was more evident in middle-aged rats. These results indicate that the prior attenuation of KiSS1 and consequent depression of LH surges plays a key role in the onset of abnormal estrous cycling in the delayed effect. (C) 2015 Elsevier Inc. All rights reserved.
机译:新生儿暴露于17α-乙炔基雌二醇(EE)会导致延迟效应,这是后期发生的不可逆转的生殖功能损害,其特征是年龄匹配的异常发情周期的早期发作。为了阐明下丘脑关键循环调节因子KiSS1 / GPR54参与延迟效应的原因,我们调查了新生的初次暴露于EE的成年幼鼠的前房室室周围核(AVPV)中的人工诱导的LH激增和KiSS1 mRNA表达,并比较了这些参数约5个月大的中年大鼠。暴露于EE的和中年大鼠的AVPV中的KiSS1 mRNA表达,KiSS1阳性细胞和KiSS1 /ERα共表达细胞的数量均下降。在暴露于EE的大鼠中,LH激增的峰面积和水平呈剂量依赖性降低,而在中年大鼠中,降低更为明显。这些结果表明,KiSS1的先前衰减和随之而来的LH波动的降低在延迟发情中异常发情循环的发作中起关键作用。 (C)2015 Elsevier Inc.保留所有权利。

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