Dendrobium nobile alkaloids modulate calcium dysregulation and neuroinflammation in Alzheimer's disease: A bioinformatic analysis

Iman Touati , Yassir Boulaamane , Mohammed Reda Britel , Amal Maurady
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Abstract

Introduction

Dendrobium nobile Lindl alkaloids, or DNLA for short, are the most active ingredients found in D.nobile, a top grade plant in Shen Nong Ben Cao Jing, with an extensive history of medicinal use in Chinese traditional medicine (TCM) as a multifunctional therapeutic agent. Recent evidence has emerged linking the neuroprotective and anti-aging effects of DNLA to their involvement in promoting autophagy of toxic amyloid-β (Aβ) plaques and modulation of key enzymes involved in the hyperphosphorylation of Tau proteins. Although amyloid buildup and the aggregation of Tau proteins are central to the onset of Alzheimer's disease (AD), evidence on how DNLA relate to other overlooked dysregulated AD-associated pathways is still lacking.

Methods

We intend on deciphering the underlying mechanisms driving the anti-AD effect of DNLA, using a combination of network analysis based on differentially expressed genes found in AD patients, target fishing, centrality analysis, enrichment analysis and hub genes identification.

Results

In total, 2069 genes were found differentially expressed in SRP181886 and a PPI network constructed with common targets between DNLA and AD. Five hub genes were identified having a discriminatory power greater than 0.7; HTR2A, GRIN2B, GABRA1, HTR2C, GRIN2A, with the former being the top bottleneck node in the network. Enrichment analysis found that DNLA exert an anti-AD effect through the regulation of the calcium signaling pathway and the serotonergic system, by modulating key receptors implicated in excitatory/inhibitory neurotransmission. Additionally, DNLA were found to modulate two subunits of NMDA receptor involved in the release of pro-inflammatory cytokines, underlying the possible involvement of DNLA in neuroinflammation.

Discussion

This further emphasizes the therapeutic value of D.nobile and the multi-target, multi-pathway potential of DNLA to counteract the deleterious effects of calcium dysregulation and excitatory toxicity in AD, while providing evidence-based rationale behind the traditional use of D. nobile in TCM.

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金钗石斛生物碱可调节阿尔茨海默病的钙失调和神经炎症:生物信息学分析
导言金钗石斛(Dendrobium nobile Lindl alkaloids,简称DNLA)是《神农本草经》中最高级植物金钗石斛中发现的最有效成分,在中国传统医学(中医)中作为一种多功能治疗药物有着广泛的药用历史。最近有证据表明,DNLA 的神经保护和抗衰老作用与它们参与促进有毒淀粉样蛋白-β(Aβ)斑块的自噬和调节参与 Tau 蛋白过度磷酸化的关键酶有关。虽然淀粉样蛋白的堆积和Tau蛋白的聚集是阿尔茨海默病(AD)发病的核心原因,但目前仍缺乏证据证明DNLA与其他被忽视的AD相关途径失调之间的关系。结果在 SRP181886 中总共发现了 2069 个差异表达基因,并构建了 DNLA 和 AD 之间具有共同靶点的 PPI 网络。其中,HTR2A、GRIN2B、GABRA1、HTR2C、GRIN2A 是该网络中最重要的瓶颈节点。富集分析发现,DNLA 通过调节与兴奋/抑制性神经递质有关的关键受体,通过调节钙信号通路和血清素能系统发挥抗AD 作用。讨论这进一步强调了金钗的治疗价值以及 DNLA 多靶点、多途径的潜力,以对抗 AD 中钙调节失调和兴奋毒性的有害影响,同时为金钗在中医药中的传统应用提供了循证依据。
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