UMR 1253, iBrain, Inserm, Université de Tours, CEDEX 1, 37032, Tours, France.
Transl Psychiatry. 2022 Sep 1;12(1):356. doi: 10.1038/s41398-022-02119-1.
The different depressive disorders that exist can take root at adolescence. For instance, some functional and structural changes in several brain regions have been observed from adolescence in subjects that display either high vulnerability to depressive symptoms or subthreshold depression. For instance, adolescents with depressive disorder have been shown to exhibit hyperactivity in hippocampus, amygdala and prefrontal cortex as well as volume reductions in hippocampus and amygdala (prefrontal cortex showing more variable results). However, no animal model of adolescent subthreshold depression has been developed so far. Our objective was to design an animal model of adolescent subthreshold depression and to characterize the neural changes associated to this phenotype. For this purpose, we used adolescent Swiss mice that were evaluated on 4 tests assessing cognitive abilities (Morris water maze), anhedonia (sucrose preference), anxiety (open-field) and stress-coping strategies (forced swim test) at postnatal day (PND) 28-35. In order to identify neural alterations associated to behavioral profiles, we assessed brain resting state metabolic activity in vivo using F-FDG PET imaging at PND 37. We selected three profiles of mice distinguished in a composite Z-score computed from performances in the behavioral tests: High, Intermediate and Low Depressive Risk (HDR, IDR and LDR). Compared to both IDR and LDR, HDR mice were characterized by passive stress-coping behaviors, low cognition and high anhedonia and anxiety and were associated with significant changes of F-FDG uptakes in several cortical and subcortical areas including prelimbic cortex, infralimbic cortex, nucleus accumbens, amygdala, periaqueductal gray and superior colliculus, all displaying higher metabolic activity, while only the thalamus was associated with lower metabolic activity (compared to IDR). LDR displayed an opposing behavioral phenotype and were associated with significant changes of F-FDG uptakes in the dorsal striatum and thalamus that both exhibited markedly lower metabolic activity in LDR. In conclusion, our study revealed changes in metabolic activities that can represent neural signatures for behavioral profiles predicting subthreshold depression at adolescence in a mouse model.
存在的不同抑郁障碍可能在青春期扎根。例如,在表现出高易患抑郁症状或亚临床抑郁的受试者中,已经观察到几个大脑区域的功能和结构变化。例如,患有抑郁障碍的青少年表现出海马体、杏仁核和前额叶皮层的过度活跃,以及海马体和杏仁核的体积减少(前额叶皮层表现出更多可变的结果)。然而,到目前为止,还没有开发出青少年亚临床抑郁的动物模型。我们的目标是设计一种青少年亚临床抑郁的动物模型,并描述与这种表型相关的神经变化。为此,我们使用了在出生后第 28-35 天评估认知能力(莫里斯水迷宫)、快感缺失(蔗糖偏好)、焦虑(旷场)和应激应对策略(强迫游泳试验)的青少年瑞士小鼠。为了确定与行为特征相关的神经改变,我们在出生后第 37 天使用 F-FDG PET 成像评估了大脑的静息状态代谢活性。我们选择了三种行为测试表现的复合 Z 分数计算出来的三种不同的小鼠特征:高、中、低抑郁风险(HDR、IDR 和 LDR)。与 IDR 和 LDR 相比,HDR 小鼠表现出被动的应激应对行为、低认知、高快感缺失和焦虑,并且与几个皮质和皮质下区域的 F-FDG 摄取的显著变化相关,包括前额叶皮层、下边缘皮层、伏隔核、杏仁核、导水管周围灰质和上丘,所有这些区域都显示出更高的代谢活性,而只有丘脑与更低的代谢活性相关(与 IDR 相比)。LDR 表现出相反的行为表型,与 F-FDG 摄取的显著变化相关,在 LDR 中,背侧纹状体和丘脑都表现出明显更低的代谢活性。总之,我们的研究揭示了代谢活性的变化,这些变化可以代表行为特征的神经特征,预测青少年亚临床抑郁的动物模型。