Abstract

Multi-Worm Tracker (MWT) is a real-time computer vision system that can simultaneously quantify motional patterns of multiple worms. MWT provides several behavioral parameters, including analysis of accurate real-time locomotion speed in the nematode, Caenorhabditis elegans. Here, we determined locomotion speed of the Alzheimer's disease (AD) transgenic strain that over-expresses human beta-amyloid1-42 (Aβ) in the neurons. The MWT analysis showed that the AD strain logged a slower average speed than the wild type (WT) worms. The results may be consistent with the observation that the AD patients with dementia tend to show deficits in physical activities, including frequent falls. The AD strain showed reduced ability of the eggs to hatch and slowed hatching of the eggs. Thus, over-expression of Aβ in neurons causes negative effects on locomotion and hatchability. This study sheds light on new examples of detrimental effects that Aβ deposits can exhibit using C. elegans as a model system. The information gathered from this study indicates that the motion tracking analysis is a cost-effective, efficient way to assess the deficits of Aβ over-expression in the C. elegans system.

Highlights

  • Alzheimer’s disease (AD) is a type of amyloidosis and is the major neurodegenerative disorder that causes dementia

  • Video images of the worms on nematode growth media (NGM) agar were captured for 3 min and the speed of the worms was determined using Multi-Worm Tracker (MWT)

  • We compared the results of the wild type (WT) and AD strains (Materials and Methods)

Read more

Summary

Introduction

Alzheimer’s disease (AD) is a type of amyloidosis and is the major neurodegenerative disorder that causes dementia. AD leads to cognitive deficits due to abnormal deposits of β-amyloid (Aβ) peptides in the brain, while CAA is characterized by vascular deposits in the central nervous system, in which hemorrhage is a major clinical feature (Samarasekera et al, 2012). In AD, deposits of the Aβ peptides arise from the proteolytic processing of amyloid precursor proteins (APP), commonly observed in patients with AD (Nicholson et al, 2012). Aβ deposits and tau tangles are well known hallmarks for AD, which may trigger inflammation worsening the disease (Nicholson et al, 2012; Jack and Holtzman, 2013). Details of clinical pathogenesis and biomarkers have been reviewed elsewhere (Jack and Holtzman, 2013)

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call