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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >CHRONIC ADMINISTRATION OF 13-C/S-RETINOIC ACID DOES NOT ALTER THE NUMBER OF SEROTONINERGIC NEURONS IN THE MOUSE RAPHE NUCLEI
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CHRONIC ADMINISTRATION OF 13-C/S-RETINOIC ACID DOES NOT ALTER THE NUMBER OF SEROTONINERGIC NEURONS IN THE MOUSE RAPHE NUCLEI

机译:长期管理13-C / S-维甲酸不会改变小鼠RAPHE核中5-羟色胺神经元的数量

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The synthetic retinoid 13-cis-retinoic acid (13-c/s-RA), prescribed for the treatment of severe nodular acne, has been linked to an increased incidence of depression. Chronic treatment studies in rodents have shown that 13-c/s-RA induces an increase in depression-related behaviours and a functional uncoupling of the hippocampus and dorsal raphe nucleus (DRN). Changes in the number of serotoninergic neurons in the DRN have been reported in depressed human patients. Given that retinoids have apoptotic effects, we hypothesized that a decrease in the number of serotoninergic neurons in the DRN or median raphe nucleus (MRN) would lead to decreased serotoninergic tone and in turn to the behavioural changes seen with 13-c/s-RA administration. Here, we used immunolabelling and unbiased stereological methods to estimate the number of serotonin (5-hydroxytryp-tamine, 5-HT) neurons in the MRN and DRN of vehicle control and 13-c/s-RA-treated adult mice. In the MRN, the number of 5-HT immunolabelled cells was 1815+-194 in control, compared with 1954+-111 in 13-c/s-RA treated tissues. The number of 5-HT immunolabelled cells was much higher in the DRN, with 7148+-377 cells in the control, compared with 7578+-424 in the 13-c/s-RA treated group. Further analysis of the DRN revealed that there were no changes in the number of 5-HT neurons within distinct subregions of the DRN. Similarly, changes in the density of serotoninergic neurons or in the volume of the MRN or DRN were not observed in 13-c/s-RA treated animals. These data show that apoptotic actions of 13-c/s-RA do not occur in vivo at drug concentrations that induce changes in depression-related behaviour and functional uncoupling of the DRN and hippocampus. The potential pro-depressant behavioural and molecular effects associated with chronic administration of 13-c/s-RA may result from changes in serotoninergic activity rather than changes in the number of serotoninergic neurons.
机译:规定用于治疗严重结节性痤疮的合成类视黄醇13-顺-视黄酸(13-c / s-RA)与抑郁症的发病率增加有关。啮齿动物的长期治疗研究表明,13-c / s-RA引起抑郁相关行为的增加以及海马体和背沟核(DRN)的功能性解偶联。据报道,在抑郁的人类患者中,DRN中5-羟色胺能神经元数量的变化。考虑到类视黄醇具有凋亡作用,我们假设DRN或正中缝核(MRN)中5-羟色胺能神经元数量的减少会导致5-羟色胺能神经张力降低,进而导致13-c / s-RA引起的行为改变行政。在这里,我们使用免疫标记和无偏见的立体方法来估计媒介物对照和13-c / s-RA治疗的成年小鼠的MRN和DRN中5-羟色胺(5-羟色胺,5-HT)神经元的数量。在MRN中,对照组的5-HT免疫标记细胞数为1815 + -194,而在13-c / s-RA处理的组织中为1954 + -111。与13-c / s-RA治疗组的7578 + -424相比,DRN中5-HT免疫标记的细胞数量高得多,对照组为7148 + -377个细胞。对DRN的进一步分析表明,在DRN的不同子区域内,5-HT神经元的数量没有变化。类似地,在13-c / s-RA治疗的动物中未观察到5-羟色胺能神经元密度或MRN或DRN体积的变化。这些数据表明,在药物浓度下13-c / s-RA的凋亡作用在体内不会发生,而药物浓度会引起抑郁相关行为的改变以及DRN和海马的功能解偶联。与13-c / s-RA的长期给药相关的潜在的促抑郁行为和分子效应可能是5-羟色胺能活性的改变而不是5-羟色胺能神经元数目的改变。

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