Publication Date

2024

Document Type

Thesis

Committee Members

Sherif M. Elbasiouny, Ph.D. (Advisor); David R. Ladle, Ph.D. (Committee Member); Tarun Goswami, D.Sc. (Committee Member)

Degree Name

Master of Science in Biomedical Engineering (MSBME)

Abstract

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease characterized by motor neuron (MN) death resulting in paralysis and eventually death. ALS has greater prevalence in older populations sharing characteristics with aging like muscle weakness and MN type specific degeneration. MNs innervate skeletal muscles and control muscle contraction through their excitability which is altered in both conditions. C-Boutons are a cholinergic, excitatory synaptic input to MNs and have been studied in ALS and aging but have produced inconsistent findings and undesired gaps. We used immunohistochemistry to label mouse lumbar spinal cord and separate MN types. 60x imaging and automated analysis was performed providing robust 3D measurements. Our results presented similar findings between two ALS mutations with differing changes in a third mutation. We also show C-Bouton input with age undergoes sex and MN type specific reductions aligning with age-related weakness. Finally, we identify C-Bouton similarities and differences between ALS and aging.

Page Count

81

Department or Program

Department of Biomedical, Industrial & Human Factors Engineering

Year Degree Awarded

2024


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