Studies of the G protein beta 3 subunit in human hypertension

I have studied the GNB3 gene as a candidate gene for hypertension and left ventricular mass in a systematic and comprehensive manner. I have carried out association studies in three independent populations - A case-control study with well characterised hypertensive and their matched controls; a twin...

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Main Author: Padmanabhan, Sandosh
Published: University of Glasgow 2004
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415256
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spelling ndltd-bl.uk-oai-ethos.bl.uk-4152562015-03-19T03:41:22ZStudies of the G protein beta 3 subunit in human hypertensionPadmanabhan, Sandosh2004I have studied the GNB3 gene as a candidate gene for hypertension and left ventricular mass in a systematic and comprehensive manner. I have carried out association studies in three independent populations - A case-control study with well characterised hypertensive and their matched controls; a twin study looking at echocardiographic LV mass; and a large family based study analysing blood pressure and ECG LV mass. In addition I have also looked at three additional candidate genes including ACE, aldosterone synthase and beta-1 adrenoceptor. Though these studies concluded that there was no association between the C825T polymorphism and blood pressure or LV mass, I have demonstrated a significant heritability of various electrocardiographic measures of LV mass and an interaction between GNB3, ACE and SF1 explaining the variability of continuous measures of LV mass in this population. I studied the functional aspects of the GNB3 polymorphism by measuring platelet aggregation in normal human volunteers, using it as a marker of G-protein related signal transduction. However, there was also no association between epinephrine or platelet activating factor induced platelet aggregation and the GNB3 genotype. Finally, I performed molecular studies using cells transfected with b3 (wild-type) and b3-s (splice-variant) of GNB3 along with a fusion construct of a2AGi, and measuring of GTPase activity and calcium signalling. There was no significant difference between b3 or b3-s transfected cells, in terms of epinephrine stimulated GTPase activity, onset-delay of calcium release and time-to-peak of calcium signal. However, cells expressing b3-s showed a significantly lower rate of calcium release compared to cells expressing b3. These results indicate that the G protein b3-s subunit has no functional difference or possible slightly reduced effect compared to the wild type.616.132071R Medicine (General)University of Glasgowhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415256http://theses.gla.ac.uk/3784/Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 616.132071
R Medicine (General)
spellingShingle 616.132071
R Medicine (General)
Padmanabhan, Sandosh
Studies of the G protein beta 3 subunit in human hypertension
description I have studied the GNB3 gene as a candidate gene for hypertension and left ventricular mass in a systematic and comprehensive manner. I have carried out association studies in three independent populations - A case-control study with well characterised hypertensive and their matched controls; a twin study looking at echocardiographic LV mass; and a large family based study analysing blood pressure and ECG LV mass. In addition I have also looked at three additional candidate genes including ACE, aldosterone synthase and beta-1 adrenoceptor. Though these studies concluded that there was no association between the C825T polymorphism and blood pressure or LV mass, I have demonstrated a significant heritability of various electrocardiographic measures of LV mass and an interaction between GNB3, ACE and SF1 explaining the variability of continuous measures of LV mass in this population. I studied the functional aspects of the GNB3 polymorphism by measuring platelet aggregation in normal human volunteers, using it as a marker of G-protein related signal transduction. However, there was also no association between epinephrine or platelet activating factor induced platelet aggregation and the GNB3 genotype. Finally, I performed molecular studies using cells transfected with b3 (wild-type) and b3-s (splice-variant) of GNB3 along with a fusion construct of a2AGi, and measuring of GTPase activity and calcium signalling. There was no significant difference between b3 or b3-s transfected cells, in terms of epinephrine stimulated GTPase activity, onset-delay of calcium release and time-to-peak of calcium signal. However, cells expressing b3-s showed a significantly lower rate of calcium release compared to cells expressing b3. These results indicate that the G protein b3-s subunit has no functional difference or possible slightly reduced effect compared to the wild type.
author Padmanabhan, Sandosh
author_facet Padmanabhan, Sandosh
author_sort Padmanabhan, Sandosh
title Studies of the G protein beta 3 subunit in human hypertension
title_short Studies of the G protein beta 3 subunit in human hypertension
title_full Studies of the G protein beta 3 subunit in human hypertension
title_fullStr Studies of the G protein beta 3 subunit in human hypertension
title_full_unstemmed Studies of the G protein beta 3 subunit in human hypertension
title_sort studies of the g protein beta 3 subunit in human hypertension
publisher University of Glasgow
publishDate 2004
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415256
work_keys_str_mv AT padmanabhansandosh studiesofthegproteinbeta3subunitinhumanhypertension
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