Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.676986
Title: Mechanisms involved in the pathophysiology of hypertension models : studies on transient receptor potential vanilloid 1 (TRPV1) and RAMP2
Author: Liang, Lihuan
ISNI:       0000 0004 5368 088X
Awarding Body: King's College London
Current Institution: King's College London (University of London)
Date of Award: 2014
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Abstract:
Hypertension has been described as an important risk factor for cardiovascular morbidity and mortality, despite current treatments. Therefore an increased understanding of the mechanisms in the development of hypertension has become essential. This project involves the study of the vascular component of murine models of hypertension. Firstly the protective role of calcitonin gene-related peptide (CGRP)-like peptide adrenomedullin (AM) was examined using transgenic mice for the AM receptor. Secondly transient receptor potential vanilloid 1 (TRPV1) was studied, activation of which is known to release the sensory neuropeptide CGRP. The angiotensin II (ATII) induced hypertension murine model is considered to mimic essential hypertension. Here, hypertension was induced in 3-4 month old mice (mixed gender) over 14 days following implantation of ATII-containing osmotic mini-pumps. Blood pressure was monitored before mini-pump implantation and until day 14 by either tail cuff plethysmography or telemetry. Post-hoc study analysis of vascular hypertrophy and vascular dysfunction biomarkers (e.g. VCAM-1 and endothelin) was performed. Studies in AM receptor transgenic mice revealed no effect on hypertension, but significant protection against aortic vascular remodelling. This indicates that adrenomedullin, like CGRP, is a protective peptide in the vasculature. Surprizingly, the TRPV1 KO mice were protected against hypertension and aortic remodelling, suggesting a lack of critical involvement of CGRP.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.676986  DOI: Not available
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