The growth of white matter during human adolescence shows a striking sexual dimorphism; the volume of white matter increases with age slightly in girls and steeply in boys. Here, we provide evidence supporting the role of androgen receptor (AR) in mediating the effect of testosterone on white matter. In a large sample of typically developing adolescents (n= 408, 204 males), we used magnetic resonance imaging and acquired T1-weighted and magnetization transfer ratio (MTR) images. We also measured plasma levels of testosterone and genotyped a functional polymorphism in the AR gene, namely the number of CAG repeats in exon 1 believed to be inversely proportional to the AR transcriptional activity. We found that the testosterone-related increase of white-matter volume was stronger in male adolescents with the lower versus higher number of CAG repeats in the AR gene, with testosterone explaining, respectively, 26 and 8% of variance in the volume. The MTR results suggest that this growth is not related to myelination; the MTR decreased with age in male adolescents. We speculate that testosterone affects axonal caliber rather than the thickness of the myelin sheath.
To date, electroconvulsive therapy (ECT) is the most potent treatment in severe depression. Although ECT has been successfully applied in clinical practice for over 70 years, the underlying mechanisms of action remain unclear. We used functional MRI and a unique data-driven analysis approach to examine functional connectivity in the brain before and after ECT treatment. Our results show that ECT has lasting effects on the functional architecture of the brain. A comparison of pre-and posttreatment functional connectivity data in a group of nine patients revealed a significant cluster of voxels in and around the left dorsolateral prefrontal cortical region (Brodmann areas 44, 45, and 46), where the average global functional connectivity was considerably decreased after ECT treatment (P < 0.05, family-wise error-corrected). This decrease in functional connectivity was accompanied by a significant improvement (P < 0.001) in depressive symptoms; the patients' mean scores on the Montgomery Asberg Depression Rating Scale pre-and posttreatment were 36.4 (SD = 4.9) and 10.7 (SD = 9.6), respectively. The findings reported here add weight to the emerging "hyperconnectivity hypothesis" in depression and support the proposal that increased connectivity may constitute both a biomarker for mood disorder and a potential therapeutic target. T he treatment of depressive disorder is one of the most pressing issues in contemporary medical practice: The illness is a leading cause of significant disability worldwide (1). Current therapeutic strategies are imperfect, and there is an urgent need to develop more consistently effective and rapidly acting treatment solutions. Unfortunately, our understanding of the etiopathology of mood disorder is incomplete. As a result, the elucidation of the mechanisms of action of effective treatment has necessarily been less than secure and advance has been slow. Available treatments (e.g., chemical antidepressant therapy) were discovered serendipitously rather than designed, and insight into the biology of depressive disorder by study of antidepressant actions has been limited. In particular, the effectiveness of electroconvulsive therapy (ECT), the most potent and rapidly acting of all antidepressant agents (2), has eluded a coherent explanatory framework despite its regular use for more than 70 years. However, if the effects of ECT could be reproduced in a less invasive way, and with a more benign side-effect profile, the treatment of severe depression would be significantly enhanced. To achieve this, we need first to understand better how ECT influences brain function. Here, we show that ECT alters the functional architecture of frontal systems by strongly down-regulating connectivity in key circuits implicated in mood disorder.Efforts to delineate the neural substrate of mood disorder using functional brain imaging technology have generally identified abnormal frontal cortical and limbic activity in depressed patients (3-9). Although such regional findings tend to correspond anatomically to tho...
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