Mental Health Theme, Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia.
The Florey Department of Neuroscience and Mental Health, The University of Melbourne, Melbourne, Australia.
J Comp Neurol. 2019 Apr 15;527(6):1039-1055. doi: 10.1002/cne.24574. Epub 2018 Dec 18.
Healthy brain function requires a balance between the activity of dopamine receptor 1 (D1) and dopamine receptor 2 (D2). Alterations in this balance increase the risk for numerous developmental brain disorders. Indeed, D1 and D2 expression fluctuates throughout maturation, although there is conflicting evidence regarding the precise changes that occur. Here, we used stereology to investigate the developmental changes in the number of D1- or D2-expressing neurons in the prelimbic cortex, infralimbic cortex (IL), insula cortex, dorsal striatum, and ventral striatum of female and male mice with green fluorescent protein-tagged D1 or D2. Postnatal day 17, 25, 35, 49, and 70 were examined to cover juvenility to adulthood. In all regions, analysis of D1 density compared to D2 density within each sex seldom detected effects or interactions involving age. However, D1:D2 density ratio changed across age depending on sex. In the IL, D1:D2 density ratio increased in females from adolescence, whereas it was stable in males. In the insula cortex, D1:D2 ratio initially increased in males but decreased in females from juvenility to preadolescence. The ratio then increased in males and females from adolescence to adulthood, with males showing a more dramatic increase. In both the dorsal and ventral striatum, the ratio increased from adolescence. In all regions, females had a higher ratio compared to males throughout maturation except in the insula cortex at P25. These comprehensive observations are novel, and highlight how the maturational changes in the expression of these receptors may contribute to developmental disorders.
健康的大脑功能需要多巴胺受体 1(D1)和多巴胺受体 2(D2)的活性之间保持平衡。这种平衡的改变会增加许多发育性脑疾病的风险。事实上,D1 和 D2 的表达在成熟过程中会波动,尽管关于确切变化存在相互矛盾的证据。在这里,我们使用体视学研究了 GFP 标记的 D1 或 D2 表达神经元在雌性和雄性小鼠的额前皮质、下边缘皮质(IL)、岛叶皮质、背侧纹状体和腹侧纹状体中的数量随发育的变化。检查了出生后第 17、25、35、49 和 70 天,以覆盖从幼年到成年的时间。在所有区域中,对每个性别内 D1 密度与 D2 密度的分析很少检测到与年龄有关的影响或相互作用。然而,D1:D2 密度比随性别而变化。在 IL 中,D1:D2 密度比在雌性中从青春期开始增加,而在雄性中则保持稳定。在岛叶皮质中,D1:D2 比率最初在雄性中增加,但在雌性中从幼年到青春期前减少。然后,该比率在雄性和雌性中从青春期增加到成年期,雄性的增加更为明显。在背侧和腹侧纹状体中,该比率从青春期开始增加。在所有区域中,除了在 P25 的岛叶皮质外,雌性在整个成熟过程中的比例都高于雄性。这些全面的观察结果是新颖的,强调了这些受体表达的成熟变化如何可能导致发育障碍。