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Full-Text Articles in Biomedical Engineering and Bioengineering
Altered Skeletal Muscle Excitation-Contraction Coupling In The R6/2 Transgenic Mouse Model For Huntington's Disease, Daniel R. Miranda
Altered Skeletal Muscle Excitation-Contraction Coupling In The R6/2 Transgenic Mouse Model For Huntington's Disease, Daniel R. Miranda
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Huntington’s disease (HD) has classically been categorized as a neurodegenerative disorder. However, the expression of the disease-causing mutated huntingtin gene in skeletal muscle may contribute to the symptoms of HD, namely those that involve involuntary muscle contraction. In the R6/2 transgenic mouse model of HD, we previously observed ion channel defects that could contribute to involuntary muscle contraction. Here, in R6/2 muscle we investigated the consequence of these ion channel defects on action potentials (APs), the first step in excitation-contraction (EC) coupling. We found that the ion channel defects were associated with depolarizing the baseline membrane potential during AP trains. …
Altered Skeletal Muscle Excitation-Contraction Coupling In The R6/2 Transgenic Mouse Model For Huntington's Disease, Daniel R. Miranda
Altered Skeletal Muscle Excitation-Contraction Coupling In The R6/2 Transgenic Mouse Model For Huntington's Disease, Daniel R. Miranda
Browse all Theses and Dissertations
Huntington’s disease (HD) has classically been categorized as a neurodegenerative disorder. However, the expression of the disease-causing mutated huntingtin gene in skeletal muscle may contribute to the symptoms of HD, namely those that involve involuntary muscle contraction. In the R6/2 transgenic mouse model of HD, we previously observed ion channel defects that could contribute to involuntary muscle contraction. Here, in R6/2 muscle we investigated the consequence of these ion channel defects on action potentials (APs), the first step in excitation-contraction (EC) coupling. We found that the ion channel defects were associated with depolarizing the baseline membrane potential during AP trains. …
The Role Of Ca2+ In Central Respiratory Control Neurons Of The Locus Coeruleus: Development Of The Chemosensitive Brake, Ann Nicole Imber
The Role Of Ca2+ In Central Respiratory Control Neurons Of The Locus Coeruleus: Development Of The Chemosensitive Brake, Ann Nicole Imber
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Chemosensitive LC neurons increase their firing rate in response to increased CO2 (hypercapnia) in part via inhibition of K+ channels. This increase gets smaller during the first two postnatal weeks (neonatal rats aged P3-P16). Alterations of this "accelerating" pathway may account for the developmental changes in the magnitude of the chemosensitive response in LC neurons. Alternatively, Ca2+ and Ca2+ channels may play a role in the response to hypercapnia, but little is known about the role of Ca2+ in central chemosensitivity. Whole cell patch clamp and fluorescence imaging microscopy were used to study a different …