Regulation of circadian gene activity in fibroblasts from ADHD patients through Rosiglitazone: a pilot study.

IF 3.2 4区 医学 Q2 CLINICAL NEUROLOGY
Journal of Neural Transmission Pub Date : 2025-05-01 Epub Date: 2025-01-30 DOI:10.1007/s00702-025-02883-6
Monica Grigore, Andrei Gresita, D M Hermann, Thorsten R Doeppner, Victor Gheorman, Daniela Glavan, Aurel Popa-Wagner
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Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a frequently observed condition, with about 70% of individuals diagnosed with ADHD experiencing irregular sleep-wake patterns. Beyond the primary symptoms of ADHD, there is a significant overlap with sleep-related issues, indicating that disrupted sleep patterns may exacerbate ADHD symptoms. ADHD-related sleep problems can be traced to a delayed circadian rhythm and a later onset of melatonin production. Therefore, normalizing circadian rhythms has been proposed as a potential therapeutic target for psychiatric disorders. Recent animal studies have provided compelling evidence linking peroxisome proliferator-activated receptor gamma (PPARγ), a key regulator of energy metabolism, to the regulation of physiological and behavioral rhythms. In this study, we hypothesized that treating fibroblasts from ADHD patients, which exhibit disturbances in circadian rhythmicity that are replicated in peripheral fibroblasts, with rosiglitazone may restore their circadian rhythmicity to that of the controls. To this end, we used cultures of fibroblasts obtained from skin biopsy explants of ADHD patients and controls and investigated the temporal patterns of clock gene expression over a period of 24 h. We report that the administration of the PPARγ agonist, rosiglitazone significantly realigns the chronobiological patterns of ADHD patient samples and control groups by inducing phase shifts in the expression of the BMAL1, PER3, and CRY1 clock genes. Nevertheless, rosiglitazone showed limited impact on the amplitude and phase of CLOCK1, NPAS2, and PER1. No notable changes were observed in PER2 and PER3 gene expression. The data from cultured human dermal fibroblasts indicate that PPARγ-agonists may help regulate circadian molecular mechanisms. Given the shared genetic pathways between ADHD and obesity, future studies could investigate the potential of RSG as a treatment for circadian rhythm disorders, particularly in obese patients with ADHD.

通过罗格列酮调节ADHD患者成纤维细胞的昼夜节律基因活性:一项初步研究。
注意缺陷/多动障碍(ADHD)是一种经常观察到的疾病,大约70%被诊断患有ADHD的人经历了不规则的睡眠-觉醒模式。除了ADHD的主要症状外,还有与睡眠相关的问题,这表明睡眠模式的中断可能会加剧ADHD的症状。与多动症相关的睡眠问题可以追溯到昼夜节律的延迟和褪黑激素分泌的延迟。因此,生理节律正常化被认为是精神疾病的潜在治疗靶点。最近的动物研究提供了令人信服的证据,证明过氧化物酶体增殖物激活受体γ (PPARγ)是能量代谢的关键调节因子,与生理和行为节律的调节有关。在这项研究中,我们假设用罗格列酮治疗ADHD患者的成纤维细胞,可以使其昼夜节律恢复到对照组的水平,这些患者表现出昼夜节律紊乱,并在周围成纤维细胞中复制。为此,我们使用了从ADHD患者和对照组的皮肤活检外植体中获得的成纤维细胞培养物,并研究了24小时内时钟基因表达的时间模式。我们报告说,PPARγ激动剂罗格列酮通过诱导BMAL1、PER3和CRY1时钟基因表达的相移,显著地重新调整了ADHD患者样本和对照组的时间生物学模式。然而,罗格列酮对CLOCK1、NPAS2和PER1的振幅和相位的影响有限。PER2和PER3基因表达无明显变化。来自培养的人真皮成纤维细胞的数据表明,ppar γ激动剂可能有助于调节昼夜节律的分子机制。考虑到ADHD和肥胖之间共享的遗传途径,未来的研究可以调查RSG作为昼夜节律障碍治疗的潜力,特别是在肥胖的ADHD患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Neural Transmission
Journal of Neural Transmission 医学-临床神经学
CiteScore
7.20
自引率
3.00%
发文量
112
审稿时长
2 months
期刊介绍: The investigation of basic mechanisms involved in the pathogenesis of neurological and psychiatric disorders has undoubtedly deepened our knowledge of these types of disorders. The impact of basic neurosciences on the understanding of the pathophysiology of the brain will further increase due to important developments such as the emergence of more specific psychoactive compounds and new technologies. The Journal of Neural Transmission aims to establish an interface between basic sciences and clinical neurology and psychiatry. It intends to put a special emphasis on translational publications of the newest developments in the field from all disciplines of the neural sciences that relate to a better understanding and treatment of neurological and psychiatric disorders.
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