Lu N Z, Eshleman A J, Janowsky A, Bethea C L
Division of Reproductive Sciences, Oregon National Primate Research Center, Beaverton, USA.
Mol Psychiatry. 2003 Mar;8(3):353-60. doi: 10.1038/sj.mp.4001243.
The serotonin reuptake transporter (SERT) plays an important role in serotonin neurotransmission and in several psychopathological disorders such as depression and anxiety disorders. In this study, we investigated whether the ovarian steroids, estrogen (E) and progesterone (P) regulate SERT binding, intracellular distribution, and function using [(3)H]citalopram ligand binding with quantitative autoradiography, immunofluorescence histochemistry with confocal microscopy and [(3)H]serotonin uptake, respectively. Ovariectomized macaques received either placebo, E alone, P alone or E plus P for 28 days. In the raphe, E, P, and E+P treatments did not change SERT binding density. In several hypothalamic nuclei, [(3)H]citalopram binding was increased by E, P, and E+P. Immunofluorescent SERT in serotonin soma was intracellular and similar among treatments. In the hypothalamus, immunofluorescent SERT was located along the serotonergic axons and there was a significant proliferation of immunofluorescent fibers in hormone-treated animals. In addition, E and E+P treatment increased serotonin uptake in the basal ganglia. These findings suggest that ovarian hormones regulate SERT protein expression and distribution, perhaps via extracellular serotonin or mRNA stability, but not solely at the level of gene transcription. Further investigation on the possible action of ovarian steroids on the directionality of SERT transport is indicated.
5-羟色胺再摄取转运体(SERT)在5-羟色胺神经传递以及多种精神病理障碍(如抑郁症和焦虑症)中发挥着重要作用。在本研究中,我们分别使用[³H]西酞普兰配体结合定量放射自显影技术、共聚焦显微镜免疫荧光组织化学技术以及[³H]5-羟色胺摄取技术,研究了卵巢类固醇激素雌激素(E)和孕激素(P)是否调节SERT结合、细胞内分布及功能。去卵巢的猕猴接受安慰剂、单独使用E、单独使用P或E加P治疗28天。在中缝核,E、P和E + P治疗均未改变SERT结合密度。在几个下丘脑核团中,E、P和E + P均使[³H]西酞普兰结合增加。5-羟色胺神经元胞体中的免疫荧光SERT位于细胞内,各治疗组之间相似。在下丘脑中,免疫荧光SERT沿5-羟色胺能轴突分布,激素治疗组动物的免疫荧光纤维有显著增生。此外,E和E + P治疗增加了基底神经节中的5-羟色胺摄取。这些发现表明,卵巢激素可能通过细胞外5-羟色胺或mRNA稳定性调节SERT蛋白表达和分布,但并非仅在基因转录水平发挥作用。有必要进一步研究卵巢类固醇对SERT转运方向性的可能作用。