Tese
Caracterização das alterações morfofuncionais de unidades motoras de um modelo murino para doença de Huntington (BACHD)
Fecha
2016-12-13Autor
Priscila Aparecida Costa Valadão
Institución
Resumen
Huntington's disease is a complex neurodegenerative disorder characterized by motor
dysfunction with severe muscle atrophy. The motor symptoms are progressive and
attributed to the loss of striatal neurons in the brain, causing involuntary limbs, trunk and
face movements. In Huntington’s disease, there is a polyglutamine expansion of
huntingtin protein leading to the formation of mutated protein that interferes in several
processes in cells leading them to the death. Despite the cause of the involuntary
movements in Huntington’s disease be well established, it is known that both normal and
mutated huntingtin are expressed outside the Central Nervous System, such as at the
skeletal muscle. Thus, the aim of this study was to investigate possible changes in
sternomastoid and tibialis anterior muscle’s motor units from a murine model for
Huntington’s disease (BACHD) once this structure is directly involved in the execution
of movements. We used behavioral tests, optical, fluorescence, confocal and electronic
microscopy to investigate possible changes in the components of sternomastoid and
tibialis anterior muscles motor units, such as motor neurons in the cervical and lumbar
segment of the spinal cord, neuromuscular junctions and skeletal muscles. We first
identified motor deficit in behavioral testes in BACHD mice. After, we observed in
transgenic mice decrease in cervical and lumbar motoneurons number and atrophy. We
also observed fragmentation, denervation and loss of pre and post-synaptic colocalization
in neuromuscular junctions. In addition, we noticed that muscle atrophy that was
accompanied by both changes in the pattern of the myosin heavy chain and muscle
ultrastructural abnormalities in both muscle. Together, our results indicate that this
muscle’ motor unit is also affected in all its components. These results can further
contribute to new targets for therapeutic interventions focusing on peripheral structures
related to movement.