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Drug-Induced Sleep Endoscopy DISE with Target Controlled Infusion TCI and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
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Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
Cira Rubies1, Ana-Paula Dantas1, Montserrat Batlle2,3
1Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Scientific Reports
|August 9, 2019
Summary
Obstructive sleep apnea causes aortic changes like hypertrophy and elastin rupture. Mesenchymal stem cell infusions may mitigate these vascular effects by reducing inflammation.
Area of Science:
- Cardiovascular Research
- Sleep Medicine
- Regenerative Medicine
Background:
- Obstructive sleep apnea (OSA) is linked to aortic issues like dilatation, stiffness, and atherosclerosis.
- The precise mechanisms driving vascular remodeling in OSA remain unclear.
Purpose of the Study:
- To investigate vascular remodeling in the aorta caused by OSA.
- To explore the underlying molecular mechanisms of OSA-induced vascular changes.
- To evaluate the therapeutic potential of mesenchymal stem cells (MSC) in a rat model of OSA.
Main Methods:
- A non-invasive rat model of chronic OSA was established using recurrent airway obstructions.
- Sham-operated rats without obstructions served as controls.
- Vascular remodeling, molecular markers (ROS, RAS, nitric oxide), and the impact of MSC infusions were assessed.
Main Results:
- Chronic OSA induced significant aortic remodeling, including eccentric hypertrophy, increased wall thickness, and lumen diameter.
- Elastin fibers in the aorta increased but showed signs of rupture; no changes in media fibrosis were observed.
- Elevated reactive oxygen species (ROS), renin-angiotensin system (RAS) markers, and nitric oxide imbalance were identified as potential mechanisms.
- MSC infusions attenuated OSA-related vascular alterations, likely via anti-inflammatory effects.
Conclusions:
- Repetitive airway obstructions mimicking OSA cause substantial structural changes in the thoracic aorta.
- Oxidative stress, RAS activation, and nitric oxide dysregulation are implicated in OSA-induced aortic remodeling.
- Mesenchymal stem cells show promise in ameliorating OSA-associated vascular damage, potentially through their anti-inflammatory actions.
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