5型磷酸二酯酶抑制剂他达拉非的抗抑郁和抗焦虑作用与中枢神经系统自身免疫过程中肠道-大脑轴的调节有关

Eduardo Duarte-Silva, Alice Chevrollier Oriá, Ingrid Prata Mendonça, Igor Henrique Rodrigues Paiva, Klyvia Leuthier Dos Santos, Amanda Juliana Sales, José Roberto Botelho de Souza, Michael Maes, Sven Guenther Meuth, Christina Alves Peixoto
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摘要

多发性硬化症(MS)是一种严重影响中枢神经系统(CNS)的衰弱性疾病。除神经系统症状外,该病还伴有焦虑和抑郁等神经精神并发症。西地那非和他达拉非等磷酸二酯酶-5抑制剂(PDE5Is)已被证明具有类似抗抑郁的作用,但这种作用的机制尚未完全确定。为了解决这个问题,我们使用了多发性硬化症的 EAE 模型、行为测试、免疫荧光、免疫组织化学、Western 印迹和 16 S rRNA 测序。在这里,我们发现实验性自身免疫性脑脊髓炎(EAE)小鼠的抑郁样行为是由于神经炎症、突触可塑性降低、谷氨酸能神经递质功能障碍、糖皮质激素受体(GR)抵抗、血脑屏障(BBB)通透性增加和免疫细胞浸润中枢神经系统以及炎症、肠道通透性增加和免疫细胞浸润远端结肠所致。此外,16 S rRNA 测序显示,EAE 小鼠的行为功能障碍与肠道微生物群的变化有关,如固着菌和糖杆菌的丰度增加,而变形菌、副杆菌和脱硫弧菌的丰度减少。此外,我们还发现 Erysipelotrichaceae 和 Desulfovibrionaceae 的数量增加,而 Lactobacillus johnsonii 的数量减少。令人惊讶的是,我们发现他达拉非可能通过针对上述疾病的所有方面发挥类似抗抑郁的作用。总之,我们的工作表明,EAE中的焦虑和抑郁样行为与神经免疫和肠道微生物群介导的大量机制有关,而他达拉非可能是通过靶向这些机制而发挥抗抑郁样作用的。了解他达拉非的这些作用机制对于为未来抑郁症患者的临床试验铺平道路非常重要。
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The Antidepressant- and Anxiolytic-Like Effects of the Phosphodiesterase Type-5 Inhibitor Tadalafil are Associated with the Modulation of the Gut-Brain Axis During CNS Autoimmunity.

Multiple Sclerosis (MS) is a debilitating disease that severely affects the central nervous system (CNS). Apart from neurological symptoms, it is also characterized by neuropsychiatric comorbidities, such as anxiety and depression. Phosphodiesterase-5 inhibitors (PDE5Is) such as Sildenafil and Tadalafil have been shown to possess antidepressant-like effects, but the mechanisms underpinning such effects are not fully characterized. To address this question, we used the EAE model of MS, behavioral tests, immunofluorescence, immunohistochemistry, western blot, and 16 S rRNA sequencing. Here, we showed that depressive-like behavior in Experimental Autoimmune Encephalomyelitis (EAE) mice is due to neuroinflammation, reduced synaptic plasticity, dysfunction in glutamatergic neurotransmission, glucocorticoid receptor (GR) resistance, increased blood-brain barrier (BBB) permeability, and immune cell infiltration to the CNS, as well as inflammation, increased intestinal permeability, and immune cell infiltration in the distal colon. Furthermore, 16 S rRNA sequencing revealed that behavioral dysfunction in EAE mice is associated with changes in the gut microbiota, such as an increased abundance of Firmicutes and Saccharibacteria and a reduction in Proteobacteria, Parabacteroides, and Desulfovibrio. Moreover, we detected an increased abundance of Erysipelotrichaceae and Desulfovibrionaceae and a reduced abundance of Lactobacillus johnsonii. Surprisingly, we showed that Tadalafil likely exerts antidepressant-like effects by targeting all aforementioned disease aspects. In conclusion, our work demonstrated that anxiety- and depressive-like behavior in EAE is associated with a plethora of neuroimmune and gut microbiota-mediated mechanisms and that Tadalafil exerts antidepressant-like effects probably by targeting these mechanisms. Harnessing the knowledge of these mechanisms of action of Tadalafil is important to pave the way for future clinical trials with depressed patients.

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Tetramerization of PKM2 Alleviates Traumatic Brain Injury by Ameliorating Mitochondrial Damage in Microglia. T Cells Trafficking into the Brain in Aging and Alzheimer's Disease. Sigma-1 Receptors Control Neuropathic Pain and Peripheral Neuroinflammation After Nerve Injury in Female Mice: A Transcriptomic Study. The Antidepressant- and Anxiolytic-Like Effects of the Phosphodiesterase Type-5 Inhibitor Tadalafil are Associated with the Modulation of the Gut-Brain Axis During CNS Autoimmunity. Hyperalgesic Effect Evoked by il-16 and its Participation in Inflammatory Hypernociception in Mice.
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