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美达加 - 一种新型复方草药制剂可改善阿尔茨海默病模型的认知行为和疾病病理。

Medha Plus - A novel polyherbal formulation ameliorates cognitive behaviors and disease pathology in models of Alzheimer's disease.

机构信息

Cell Biology and Physiology Division, CSIR-Indian Institute of Chemical Biology, 4 Raja S. C. Mullick Road, Kolkata 700032, India.

Cell Biology and Physiology Division, CSIR-Indian Institute of Chemical Biology, 4 Raja S. C. Mullick Road, Kolkata 700032, India; Academy of Scientific and Innovative Research (AcSIR), Headquarters, CSIR-HRDC Campus, Sector 19, Kamla Nehru Nagar, Ghaziabad 201002, India.

出版信息

Biomed Pharmacother. 2022 Jul;151:113086. doi: 10.1016/j.biopha.2022.113086. Epub 2022 May 24.

Abstract

Alzheimer's disease (AD) is a multi-faceted neurodegenerative disorder that leads to drastic cognitive impairments culminating in death. Pathologically, it is characterized by amyloid-β (Aβ) plaques, neurofibrillary tangles and neurodegeneration in brain. Complete cure of AD remains elusive to date. Available synthetic drugs only provide symptomatic reliefs targeting single molecule, hence, are unable to address the multi-factorial aspects in AD pathogenesis. It is imperative to develop combinatorial drugs that address the multiple molecular targets in AD. We show a unique polyherbal formulation of Brahmi, Mandukaparni, Shankhpushpi, Yastimadhu, Kokilaksha and Shunthi called 'Medha Plus' (MP), conventionally used for improving memory and reducing anxiety, was able to ameliorate cognitive deficits and associated pathological hallmarks of AD. Viability assays revealed that MP prevented Aβ-induced loss of neurites as well as neuronal apoptosis in cellular models. An array of behavioral studies showed that MP was able to recover AD-associated memory deficits in both Aβ-injected rats and 5XFAD mice. Immunohistochemical studies further revealed that MP treatment reduced Aβ depositshpi and decreased apoptotic cell death in the hippocampus. Enzymatic assays demonstrated anti-oxidative and anti-acetyl cholinesterase properties of MP especially in hippocampus of Aβ-injected rats. An underlying improvement in synaptic plasticity was observed with MP treatment in 5XFAD mice along with an increased expression of phospho-Akt at serine 473 indicating a role of PI3K/Akt signaling in correcting these synaptic deficits. Thus, our strong experiment-driven approach shows that MP is an incredible combinatorial drug that targets multiple molecular targets with exemplary neuroprotective properties and is proposed for clinical trial.

摘要

阿尔茨海默病(AD)是一种多方面的神经退行性疾病,导致严重的认知障碍,最终导致死亡。从病理学上讲,它的特征是淀粉样β(Aβ)斑块、神经原纤维缠结和大脑神经退行性变。迄今为止,AD 的完全治愈仍然难以实现。现有的合成药物仅提供针对单个分子的对症治疗,因此无法解决 AD 发病机制中的多因素方面。开发针对 AD 中多个分子靶点的联合药物势在必行。我们展示了一种独特的 Brahmi、Mandukaparni、Shankhpushpi、Yastimadhu、Kokilaksha 和 Shunthi 的草药配方,称为“Medha Plus”(MP),传统上用于改善记忆和减轻焦虑,它能够改善 AD 的认知缺陷和相关病理特征。细胞活力测定表明,MP 可防止 Aβ诱导的神经突损失和细胞凋亡。一系列行为研究表明,MP 能够恢复 Aβ 注射大鼠和 5XFAD 小鼠的 AD 相关记忆缺陷。免疫组织化学研究进一步表明,MP 治疗可减少海马中的 Aβ 沉积和凋亡细胞死亡。酶促测定表明,MP 具有抗氧化和抗乙酰胆碱酯酶特性,特别是在 Aβ 注射大鼠的海马中。在 5XFAD 小鼠中,随着 MP 治疗,观察到突触可塑性的改善,磷酸化 Akt 在丝氨酸 473 处的表达增加,表明 PI3K/Akt 信号通路在纠正这些突触缺陷中的作用。因此,我们强有力的实验驱动方法表明,MP 是一种令人难以置信的组合药物,针对多个分子靶点,具有出色的神经保护特性,并被提议进行临床试验。

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