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The compensatory expression of reproductive hormone receptors in the thymus of the male rat following active immunization against GnRH

机译:主动免疫GnRH后雄性大鼠胸腺中生殖激素受体的补偿性表达

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To determine whether hormone-receptor signaling pathways in the thymus are altered by active immunization against gonadotrophin-releasing hormone I (GnRH), 3-week-old Sprague-Dawley male rats received GnRH-tandem-OVA peptides (200 μg/ml), and the effects were compared to a control group. Serum testosterone, LH and FSH concentrations were markedly reduced, with severe testicular atrophy, compared to controls, demonstrating effective blockade of the pituitary-gonadal axis. The reduction in LH and FSH concentrations in the thymus of immunized animals was lower than that observed in the serum, where a significant difference (P< 0.001) in concentration was observed between both groups. Concentrations of GnRH were increased in the thymus of immunized rats. In thymic tissue, GnRHR, FSHR and LHR demonstrated stronger immunostaining, and AR weaker staining, in the immunized group compared to controls. Reproductive hormone receptor mRNA expression was consistent with protein variations in the immunized thymus. Compared to controls, GnRHR gene levels were significantly increased (P< 0.05), however, AR mRNA expression were greatly decreased with immune week-age (P< 0.05). Both FSHR and LHR mRNA expression levels were significantly higher in the treated group than in controls in the first three samples (P< 0.05). When GnRHR was blocked by an antagonist in thymocytes, all reproductive hormone receptor gene expressions were significantly increased (P< 0.001). In summary, these findings suggest that active immunization against GnRH can up-regulate GnRH receptor and gonadotropin receptor signaling, by stimulating thymic autocrine and paracrine function, whereas the androgen receptor is down-regulated due to a lack of testosterone secretion in the thymus.
机译:为了确定是否通过主动免疫促性腺激素释放激素I(GnRH)来改变胸腺中的激素受体信号通路,三周大的Sprague-Dawley雄性大鼠接受了GnRH-串联-OVA肽(200μg/ ml),并将效果与对照组进行比较。与对照组相比,血清睾丸激素,LH和FSH浓度明显降低,并伴有严重的睾丸萎缩,表明垂体-性腺轴被有效阻断。免疫动物的胸腺中LH和FSH浓度的降低低于血清中的降低,血清中两组之间的浓度差异显着(P <0.001)。免疫大鼠的胸腺中GnRH的浓度增加。在胸腺组织中,与对照组相比,免疫组中的GnRHR,FSHR和LHR表现出更强的免疫染色,AR染色更弱。生殖激素受体mRNA的表达与免疫胸腺中的蛋白质变化一致。与对照组相比,GnRHR基因水平显着升高(P <0.05),但是随着免疫周龄的增长,AR mRNA表达大大降低(P <0.05)。在前三个样品中,治疗组的FSHR和LHR mRNA表达水平均显着高于对照组(P <0.05)。当胸腺细胞中的拮抗剂阻断GnRHR时,所有生殖激素受体基因的表达均显着增加(P <0.001)。总之,这些发现表明,通过刺激胸腺自分泌和旁分泌功能,针对GnRH的主动免疫可以上调GnRH受体和促性腺激素受体的信号传导,而由于胸腺中缺乏睾丸激素分泌,雄激素受体被下调。

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