Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.752999
Title: Impacts of inflammatory mediators and hypoxia on vascular reactivity : a model of COPD
Author: Gassama, Abubacarr Kawsu
ISNI:       0000 0004 7426 106X
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2018
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Abstract:
Chronic obstructive pulmonary disease (COPD) is characterized with a poorly reversible airflow limitation. It is a major public health challenge in many developed countries. Cardiovascular complication is a common comorbidity in COPD and is linked to hypoxia and inflammation. Arterial stiffness is also correlated with emphysema severity in COPD patients, with a suggestion that this might be related to systemic inflammation. In this thesis, we have looked to identify the potential interaction of hypoxia and inflammation upon arterial stiffness of alpha-1 antitrypsin deficient subjects. In addition, we investigated the influence of inflammatory mediators and hypoxia on vascular dysfunction in an in vivo and in vitro rat model. Our results have shown that serum TN F-a levels correlated positively and significantly with arterial stiffness as measured by pulse wave velocity (PWV). Regression analysis revealed that TNF-a is not an independent predictor of PWV. However, when combined in a regression model with age, sex, Forced Expiratory Volume in 1 second, systolic pressure and gas transfer factor TLCO, The model was effectively able to predict PWV. There was no significant interaction observed between hypoxia and inflammation to modulate arterial stiffness. In a rat model, we found that TNF-a had significant effect upon pulmonary vascular dilatation in response to carbachol and sodium nitroprusside. Hypoxia applied for 1-2 weeks in vivo had no effect upon of vascular reactivity. However, when combined with hypoxia, the effect ofTNF-a on vasodilation was further impaired. These data suggest that a combination of inflammation and hypoxia can have a combined and detrimental effect upon vascular reactivity and so provide a potential model for studying these exacerbations in vitro.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.752999  DOI: Not available
Keywords: QH301 Biology
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