Bioactive Natural Products and Synthetic Small Molecules as Potential Investigational Treatments for Neurodegenerative Diseases

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Neurobiology and Clinical Neuroscience".

Deadline for manuscript submissions: closed (30 September 2021)

Special Issue Editors


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Guest Editor
Graduate Institute of Pharmacognosy, Taipei Medical University, Taipei, Taiwan
Interests: functional activities of protein/peptides; antioxidant/antiaging activities; metabolic syndrome disorders
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Guest Editor
Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan
Interests: protein misfolding; amyloid; prion; Alzheimer’s disease; protein chemistry; peptide chemistry; biophysics
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Graduate institute of Pharmacognosy, Taipei Medical University, Taipei, Taiwan
Interests: medical chemistry; enzyme activity
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

The prevalence of Alzheimer’s disease (AD) is continuously growing worldwide, which leads to great social–economic burdens. Despite the great therapeutic improvement researchers have achieved in the past few decades, novel treatments targeting Alzheimer’s disease remain an urgent need.

AD is a progressive neurodegenerative disorder, and patients are characterized by dysfunctions of behaviors, memories, and spatial awareness and, in the late stage, loss of ability to participate in general activities. The neuropathology may involve protein abnormalities of neurofibrillary tangles of tau proteins and senile amyloid plaques of amyloid b peptides (Ab), and neuronal and synaptic losses and accompanying lower levels of acetylcholine, inflammations, and oxidative damages. The “amyloid hypothesis” is the main AD etiology for the imbalance of production and clearance of Ab, which aggregates and then accumulates to initiate AD progress. Reactive oxygen species (ROS) and free radicals are associated with aging based on the “free radical theory of aging”. Although researchers have devoted themselves to developing small molecules and monoclonal antibodies as AD treatments in recent decades, none so far have been clinically successful in cognition improvement. The poor outcome is due to the multifactorial pathogenetic mechanism of AD, and to date, the only approved therapeutic drugs for clinical AD treatments are acetylcholinesterase (AChE) inhibitors, which are developed based on the “cholinergic hypothesis”, and one N-methyl-D-aspartate (NMDA) receptor antagonist. While these drugs have shown short-term benefits in improving symptoms, however, they have not been found to be able to reverse or delay AD progression. This clearly indicates that an unmet medical need exists in AD.

The scope of this Research Topic is to investigate the potential efficacy, pharmacokinetics, and underlying mechanisms of natural products or synthetic compounds against Alzheimer’s disease using modern tools on the following subtopics but not limited to:

Subtopics:

  • Small molecular drugs and medicinal plants potentially against Alzheimer’s disease, and the in vivo pharmacokinetic properties;
  • AChE inhibitory assay and molecular docking with AChE;
  • Ab aggregation, tau protein hyperphosphorylation and neurofibrillary tangles, reactive oxygen species, neuron or microglia inflammation and their roles in neurodegeneration in cell or animal models;
  • In vitro and/or in vivo models studying natural products, synthetic compounds, or derivatives.

You may choose our Joint Special Issue in CIMB.

Prof. Dr. Wen-Chi Hou
Dr. Rita P.-Y. Chen
Prof. Dr. Wei-Jan Huang
Guest Editors

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Keywords

  • Alzheimer’s disease
  • amyloid beta
  • antioxidant
  • reactive oxygen species
  • tau protein
  • cell line experiment
  • animal models
  • bioactive natural products
  • synthetic compounds or derivatives
  • medicinal chemistry
  • computational chemistry

Published Papers (1 paper)

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Research

13 pages, 3040 KiB  
Article
Heat Shock Cognate 70 kDa Protein Is the Target of Tetradecyl 2,3-Dihydroxybenzoate for Neuritogenic Effect in PC12 Cells
by Lihong Cheng, Yanhui Wang, Lan Xiang and Jianhua Qi
Biomedicines 2021, 9(10), 1483; https://doi.org/10.3390/biomedicines9101483 - 16 Oct 2021
Cited by 2 | Viewed by 2620
Abstract
Tetradecyl 2,3-dihydroxybenzoate (ABG-001) is a lead compound derived from gentisides with a remarkable neuritogenic activity. However, the target of ABG-001 is yet to be defined to date. In this study, the potential target of ABG-001 was investigated via an activity-based protein profiling (ABPP) [...] Read more.
Tetradecyl 2,3-dihydroxybenzoate (ABG-001) is a lead compound derived from gentisides with a remarkable neuritogenic activity. However, the target of ABG-001 is yet to be defined to date. In this study, the potential target of ABG-001 was investigated via an activity-based protein profiling (ABPP) analysis, which is a chemical proteomic method for target identification by using chemical probes. Results indicated that the potential target proteins of ABG-001 were heat shock cognate 70 kDa protein (Hsc70), 78 kDa glucose-regulated protein (GRP78), and 14-3-3 theta protein. Then, the potential target of ABG-001 was confirmed by using inhibitors, the cellular thermal shift assay (CETSA) and small-interfering RNA (siRNA) analysis. The inhibitor of Hsc70 and siRNA significantly decreased the neurite outgrowth induced by ABG-001. Furthermore, ABG-001 induced neurite outgrowth was reduced by siRNA against Hsc70, and the results of CETSA suggested that Hsc70 showed a significant thermal stability-shifted effect upon ABG-001 treatment. These results indicated that Hsc70 is the target protein of ABG-001 in PC12 cells. Full article
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