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大豆黄酮在自闭症实验模型中通过激活神经元 AC/cAMP/CREB/PKA 和线粒体 ETC 复合物途径的治疗效果:来自 CSF、血浆和大脑分析的证据。

Therapeutic efficacy of Genistein in activation of neuronal AC/cAMP/CREB/PKA and mitochondrial ETC-Complex pathways in experimental model of autism: Evidence from CSF, blood plasma and brain analysis.

机构信息

Division of Neuroscience, Department of Pharmacology, ISF College of Pharmacy, Moga, Punjab, India; Affiliated to IK Gujral Punjab Technical University, Jalandhar, Punjab 144603, India.

Division of Neuroscience, Department of Pharmacology, ISF College of Pharmacy, Moga, Punjab, India; Affiliated to IK Gujral Punjab Technical University, Jalandhar, Punjab 144603, India.

出版信息

Brain Res. 2025 Jan 1;1846:149251. doi: 10.1016/j.brainres.2024.149251. Epub 2024 Oct 9.

Abstract

Autism is a complex neurodevelopmental condition characterized by repetitive behaviors, impaired social communication, and various associated conditions such as depression and anxiety. Its multifactorial etiology includes genetic, environmental, dietary, and gastrointestinal contributions. Pathologically, Autism is linked to mitochondrial dysfunction, oxidative stress, neuroinflammation, and neurotransmitter imbalances involving GABA, glutamate, dopamine, and oxytocin. Propionic acid (PRPA) is a short-chain fatty acid produced by gut bacteria, influencing central nervous system functions. Elevated PRPA levels can exacerbate Autism-related symptoms by disrupting metabolic processes and crossing the blood-brain barrier. Our research investigates the neuroprotective potential of Genistein (GNT), an isoflavone compound with known benefits in neuropsychiatric and neurodegenerative disorders, through modulation of the AC/cAMP/CREB/PKA signaling pathway and mitochondrial ETC complex (I-IV) function. In silico analyses revealed GNT's high affinity for these targets. Subsequent in vitro and in vivo experiments using a PRPA-induced rat model of autism demonstrated that GNT (40 and 80 mg/kg., orally) significantly improves locomotion, neuromuscular coordination, and cognitive functions in PRPA-treated rodents. Behavioral assessments showed reduced immobility in the forced swim test, enhanced Morris water maze performance, and restored regular locomotor activity. On a molecular level, GNT restored levels of key signaling molecules (AC, cAMP, CREB, PKA) and mitochondrial complexes (I-V), disrupted by PRPA exposure. Additionally, GNT reduced neuroinflammation and apoptosis, normalized neurotransmitter levels, and improved the complete blood count profile. Histopathological analyses confirmed that GNT ameliorated PRPA-induced brain injuries, restored normal brain morphology, reduced demyelination, and promoted neurogenesis. The study supports GNT's potential in autism treatment by modulating neural pathways, reducing inflammation, and restoring neurotransmitter balance.

摘要

自闭症是一种复杂的神经发育障碍,其特征是重复行为、社交沟通障碍以及抑郁和焦虑等各种相关病症。其多因素病因包括遗传、环境、饮食和胃肠道因素。从病理学角度来看,自闭症与线粒体功能障碍、氧化应激、神经炎症以及涉及 GABA、谷氨酸、多巴胺和催产素的神经递质失衡有关。丙酸(PRPA)是一种由肠道细菌产生的短链脂肪酸,影响中枢神经系统功能。升高的 PRPA 水平通过破坏代谢过程和穿过血脑屏障,加剧与自闭症相关的症状。我们的研究通过调节 AC/cAMP/CREB/PKA 信号通路和线粒体电子传递链(ETC)复合物(I-IV)功能,研究了染料木黄酮(GNT)这种具有神经精神和神经退行性疾病治疗益处的异黄酮化合物的神经保护潜力。计算机分析显示 GNT 与这些靶点具有高亲和力。随后使用 PRPA 诱导的自闭症大鼠模型进行的体外和体内实验表明,GNT(40 和 80mg/kg,口服)可显著改善 PRPA 处理的啮齿动物的运动、神经肌肉协调性和认知功能。行为评估显示强迫游泳试验中不动时间减少,Morris 水迷宫表现增强,以及恢复正常的运动活动。在分子水平上,GNT 恢复了被 PRPA 暴露破坏的关键信号分子(AC、cAMP、CREB、PKA)和线粒体复合物(I-V)的水平。此外,GNT 减少了神经炎症和细胞凋亡,使神经递质水平正常化,并改善了全血细胞计数谱。组织病理学分析证实 GNT 通过调节神经通路、减轻炎症和恢复神经递质平衡,改善了 PRPA 诱导的脑损伤。该研究支持 GNT 通过调节神经通路、减轻炎症和恢复神经递质平衡,在自闭症治疗中的潜在应用。

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