Aarestrup Malene Ravn, Reveles Jensen Kristian H, Larsen Søren Vinther, Ozenne Brice, Köhler-Forsberg Kristin, Knudsen Gitte Moos, Jørgensen Martin Balslev, Frokjaer Vibe G
Neurobiology Research Unit, Rigshospitalet, Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Neurosci Appl. 2025 Feb 28;4:105517. doi: 10.1016/j.nsa.2025.105517. eCollection 2025.
Sex hormones may contribute to the pathophysiology of Major Depressive Disorder (MDD) through effects on the serotonergic brain system. Estradiol is associated with serotonergic neurobiology in rodent models and humans across sexes. In healthy men, we have previously observed a negative association between testosterone and serotonin 4 receptor (5-HT4R) levels, a receptor implicated in depression and a promising novel antidepressant target. Here, we investigate the associations between sex hormone levels and 5-HT4R binding in unmedicated men with MDD compared to healthy men. We used a latent variable model to evaluate the association between estradiol and testosterone, and cerebral 5-HT4R binding based on [C]SB207145 Positron Emission Tomography (PET) data from 25 males with MDD from the Neuropharm trial and 52 healthy males (aged 18-49), which included 38 healthy males from our previous study. As previously shown in the complete group of men and women with MDD from the Neuropharm trial, we here confirm that a lower cerebral 5-HT4R level is also observed in the male MDD population alone compared to healthy men (β = -0.07, = 0.012). In addition to the previously shown negative association between global 5-HT4R levels and testosterone (β = -0.007, = 0.006) in healthy men, we also observe a positive association with estradiol (β = 1.74, = 0.001). However, we do not observe this in men with MDD (testosterone: β = 0.0001, = 0.97; estradiol: β = 0.64, 0.36). There was a trend towards a group difference in the association between testosterone and global 5-HT4R (β = 0.008, = 0.082). In summary, we found evidence for a coupling between 5-HT4R and sex hormone levels in healthy men. This neuroendocrine connection appeared unclear in unmedicated men with depression, possibly due to a different and weaker coupling.
性激素可能通过对血清素能脑系统的作用,参与重度抑郁症(MDD)的病理生理过程。在啮齿动物模型和不同性别的人类中,雌二醇都与血清素能神经生物学相关。在健康男性中,我们之前观察到睾酮与血清素4受体(5-HT4R)水平之间存在负相关,该受体与抑郁症有关,也是一个有前景的新型抗抑郁靶点。在此,我们研究了未接受药物治疗的MDD男性与健康男性相比,性激素水平与5-HT4R结合之间的关联。我们使用潜在变量模型,基于来自神经药理学试验的25名患有MDD的男性和52名健康男性(年龄在18 - 49岁之间,其中38名健康男性来自我们之前的研究)的[C]SB207145正电子发射断层扫描(PET)数据,评估雌二醇和睾酮与大脑5-HT4R结合之间的关联。正如之前在神经药理学试验中完整的MDD男性和女性群体中所显示的那样,我们在此证实,与健康男性相比,仅男性MDD群体中也观察到较低的大脑5-HT4R水平(β = -0.07, = 0.012)。除了之前在健康男性中显示的全局5-HT4R水平与睾酮之间的负相关(β = -0.007, = 0.006)外,我们还观察到与雌二醇存在正相关(β = 1.74, = 0.001)。然而,在患有MDD的男性中我们未观察到这种情况(睾酮:β = 0.0001, = 0.97;雌二醇:β = 0.64,0.36)。睾酮与全局5-HT4R之间的关联存在组间差异的趋势(β = 0.008, = 0.082)。总之,我们发现了健康男性中5-HT4R与性激素水平之间存在耦合的证据。这种神经内分泌联系在未接受药物治疗的抑郁症男性中似乎不明确,可能是由于不同且较弱的耦合。