Dystrophin as a novel regulator of the circadian clock in skeletal muscle and the brain
Active Project Grant Awarded Last action
- Award ID
- R21NS140497
- Recipient
-
University Of Alabama At Birmingham UEI YND4PLMC9AN7
- Awarding agency
-
National Institute of Neurological Disorders and Stroke
National Institutes of Health, Department of Health and Human Services
- Obligated
- $660,448
Award facts
- Assistance listing
- 93.853 Extramural Research Programs in the Neurosciences and Neurological Disorders
- Completion date 95% complete
- Place of performance
- Birmingham, AL 35294, USA
Award details come from USAspending.gov.
Description
- Abstract
- Duchenne muscular dystrophy (DMD) is a severe and progressive neuromuscular disease that affects 1:5000 live male births, making IT the most common form of muscular dystrophy. DMD is caused by the disruption of the dystrophin gene that results in the production of a non-functional or absent dystrophin protein. Lack of dystrophin in muscle results in myofiber death and fibrosis that can result in fatal cardiac arrhythmia and/or respiratory failure in end-stage DMD patients. Interestingly, many DMD patients report sleep disruption, nighttime sleep/wake disruptions, nocturnal blood pressure dipping, and other symptoms independent of diaphragm respiratory muscle weakness. These symptoms are strongly influenced by the circadian system, which suggests that DMD patients exhibit dysregulated circadian rhythmicity of which root molecular cause has not been directly identified. While the loss of dystrophin is the primary cause of DMD, IT is evident that the circadian clock has the ability to influence many of the same muscle health parameters, such as muscle function and metabolism, and may represent a novel pathological factor influencing DMD patient outcomes. This proposal will investigate the contribution of circadian rhythm disruption to DMD disease pathology and the mechanism of action to induce disease-associated pathophysiologies through the use of a novel conditional dystrophin loss-of-function mouse model. This proposal will evaluate the contribution of dystrophin expression in the skeletal muscle and suprachiasmatic nucleus (SCN)/brain towards the regulation of circadian rhythm, and define its role in muscular health and disease pathogenesis.
Transactions
| Action | Obligated | Date |
|---|---|---|
| Amendment | $187,316 | |
| Amendment | $236,566 | |
| Original award | $236,566 |
Subawards
| Subrecipient | Amount | Awarded |
|---|---|---|
| University Of Florida | $64,000 |
Quick answers
Who received award R21NS140497?
R21NS140497 was awarded to University Of Alabama At Birmingham by National Institute of Neurological Disorders and Stroke (National Institutes of Health) on December 23, 2024.
How much is award R21NS140497 worth?
$660,448 has been obligated on R21NS140497.
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