首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Sex-related differences in the distribution of opioid receptor-like 1 receptor mRNA and colocalization with estrogen receptor mRNA in neurons of the spinal trigeminal nucleus caudalis in the rat.
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Sex-related differences in the distribution of opioid receptor-like 1 receptor mRNA and colocalization with estrogen receptor mRNA in neurons of the spinal trigeminal nucleus caudalis in the rat.

机译:大鼠脊髓三叉神经尾核神经元中类阿片受体样1受体mRNA的分布以及与雌激素受体mRNA共定位的性别相关差异。

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We recently reported that exogenously applied orphanin FQ, the endogenous ligand for opioid receptor-like 1 (ORL(1)) receptor, produces sex-specific modulation of trigeminal nociception, and that estrogen contributes to these sex-related differences. Estrogen could produce these sex-related differences by altering the expression of the ORL(1)-receptor gene in the trigeminal nucleus caudalis. Utilizing in situ hybridization, we compared levels of ORL(1) receptor mRNA and investigated its colocalization with estrogen receptor mRNA in trigeminal neurons. Our results showed that in male rats, ORL(1) receptor mRNA is abundantly expressed in the rostral part of the trigeminal nucleus caudalis, and at the junction of caudalis and interpolaris (Vc/Vi). In comparison with males, levels of ORL(1) receptor mRNA were not significantly different in proestrus females, but were significantly higher in the rostral trigeminal nucleus caudalis and at the junction of Vc/Vi of diestrus females. In addition, ovariectomy raised the levels in the rostral trigeminal nucleus caudalis, and at the junction of Vc/Vi. Levels were reduced to proestrus levels in these regions following estradiol replacement. Our results also showed that ORL(1) receptor mRNA is present in majority of estrogen receptor (alpha and/or beta) mRNA-containing neurons. We conclude that there are sex-related differences in the ORL(1)-receptor gene expression in the trigeminal nucleus caudalis, which appear to be determined in part by estrogen levels.
机译:我们最近报道,外源应用的孤儿蛋白FQ,阿片受体样1(ORL(1))受体的内源性配体,产生三叉神经痛的性别特异性调节,而雌激素促成这些性别相关的差异。雌激素可通过改变三叉神经尾核中ORL(1)-受体基因的表达来产生这些性别相关的差异。利用原位杂交,我们比较了ORL(1)受体mRNA的水平,并研究了它在三叉神经元中与雌激素受体mRNA的共定位。我们的结果表明,在雄性大鼠中,ORL(1)受体mRNA在三叉神经尾鳍的前额部分以及尾鳍和极间的交界处(Vc / Vi)大量表达。与雄性相比,雌激素的雌激素水平没有显着差异,但是在雌性三叉神经的前额三叉神经尾核和雌激素的Vc / Vi交界处,ORL(1)受体mRNA的水平却明显较高。此外,卵巢切除术提高了尾状三叉神经尾状尾核和Vc / Vi交界处的水平。雌二醇替代后,这些区域的水平降低至发情期水平。我们的结果还表明,ORL(1)受体mRNA存在于大多数含雌激素受体(α和/或β)mRNA的神经元中。我们得出结论,三叉神经尾尾中的ORL(1)-受体基因表达存在性别相关差异,这似乎部分取决于雌激素水平。

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