scholarly journals Spatial structure of beta-amyloid Aβ<sub>1-40</sub> in complex with a biological membrane model

2012 ◽  
Vol 01 (03) ◽  
pp. 22-29 ◽  
Author(s):  
Konstantin S. Usachev ◽  
Andrey V. Filippov ◽  
Oleg N. Antzutkin ◽  
Vladimir V. Klochkov
2012 ◽  
Vol 50 (12) ◽  
pp. 784-792 ◽  
Author(s):  
Konstantin S. Usachev ◽  
Sergej V. Efimov ◽  
Ajdar R. Yulmetov ◽  
Andrey V. Filippov ◽  
Oleg N. Antzutkin ◽  
...  

2017 ◽  
Vol 14 (1) ◽  
Author(s):  
Wen Fu ◽  
Vlatka Vukojevic ◽  
Aarti Patel ◽  
Rania Soudy ◽  
David MacTavish ◽  
...  
Keyword(s):  

RSC Advances ◽  
2016 ◽  
Vol 6 (34) ◽  
pp. 28171-28186 ◽  
Author(s):  
Pravin Ambure ◽  
Kunal Roy

Beta (β)-site amyloid precursor protein cleaving enzyme 1 (BACE1) is one of the most important targets in Alzheimer's disease (AD), which is responsible for production and accumulation of beta amyloid (Aβ).


Author(s):  
Youngsun Lee ◽  
Yoori Choi ◽  
Eun-Joo Park ◽  
Seokjun Kwon ◽  
Hyun Kim ◽  
...  

AbstractDrainage of parenchymal waste through the lymphatic system maintains brain homeostasis. Age-related changes of glymphatic-lymphatic clearance lead to the accumulation beta-amyloid (Aβ) in dementia models. In this study, focused ultrasound treatment in combination with microbubbles (FUS-MB) improved Aβ drainage in early dementia model mice, 5XFAD. FUS-MB enhanced solute Aβ clearance from brain, but not plaques, to cerebrospinal fluid (CSF) space and then deep cervical lymph node (dCLN). dCLN ligation exaggerated memory impairment and progress of plaque formation and also the beneficial effects of FUS-MB upon Aβ removal through CSF-lymphatic routes. In this ligation model, FUS-MB improved memory despite accumulation of Aβ in CSF. In conclusion, FUS-MB enhances glymphatic-lymphatic clearance of Aβ mainly by increasing brain-to-CSF Aβ drainage. We suggest that FUS-MB can delay dementia progress in early period and benefits of FUS-MB depend on the effect of Aβ disposal through CSF-lymphatics.


2021 ◽  
Vol 18 (1) ◽  
pp. 80-87
Author(s):  
Elaine W.L. Chan ◽  
Emilia T.Y. Yeo ◽  
Kelly W.L. Wong ◽  
Mun L. See ◽  
Ka Y. Wong ◽  
...  

Background: In Alzheimer’s disease, accumulation of beta amyloid (Aβ) triggers amyloidogenesis and hyperphosphorylation of tau protein leading to neuronal cell death. Piper sarmentosum Roxb. (PS) is a traditional medicinal herb used by Malay to treat rheumatism, headache and boost memory. It possesses various biological effects, such as anti-cholinergic, anti-inflammatory, anti-oxidant and anti-depressant-like effects. Objective: The present study aimed to investigate neuroprotective properties of PS against Aβ-induced neurotoxicity and to evaluate its potential mechanism of action. Methods: Neuroprotective effects of hexane (HXN), dichloromethane (DCM), ethyl acetate (EA) and methanol (MEOH) extracts from leaves (L) and roots (R) of PS against Aβ-induced neurotoxicity were investigated in SH-SY5Y human neuroblastoma cells. Cells were pre-treated with PS for 24 h followed by 24 h of induction with Aβ. The neuroprotective effects of PS were studied using cell viability and cellular reactive oxygen species (ROS) assays. The levels of extracellular Aβ and tau proteins phosphorylated at threonine 231 (pT231) were determined. Gene and protein expressions were assessed using qRT-PCR analyses and western blot analyses, respectively. Results: Hexane extracts of PS (LHXN and RHXN) protected SH-SY5Y cells against Aβ-induced neurotoxicity, and decreased levels of extracellular Aβ and phosphorylated tau (pT231). Although extracts of PS inhibited Aβ-induced ROS production, it was unlikely that neuroprotective effects were simply due to the anti-oxidant capacity of PS. Further, mechanistic study suggested that the neuroprotective effects of PS might be due to its capability to regulate amyloidogenesis through the downregulation of BACE and APP. Conclusion: These findings suggest that hexane extracts of PS confer neuroprotection against Aβ- induced neurotoxicity in SH-SY5Y cells by attenuating amyloidogenesis and tau hyperphosphorylation. Due to its neuroprotective properties, PS might be a potential therapeutic agent for Alzheimer’s disease.


2020 ◽  
pp. 114689
Author(s):  
Stéphanie Andrade ◽  
Maria João Ramalho ◽  
Joana Angélica Loureiro ◽  
Maria Carmo Pereira

2011 ◽  
Vol 8 (1) ◽  
pp. 79 ◽  
Author(s):  
Adam D Bachstetter ◽  
Bin Xing ◽  
Lucia de Almeida ◽  
Edgardo R Dimayuga ◽  
D Martin Watterson ◽  
...  

2015 ◽  
Vol 76 ◽  
pp. 81-90 ◽  
Author(s):  
Giuseppe Verdile ◽  
Prita R. Asih ◽  
Anna M. Barron ◽  
Eka.J. Wahjoepramono ◽  
Lars M. Ittner ◽  
...  

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