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dc.contributor.authorF. du Toit, Eugeneen_US
dc.contributor.authorNabben, Marindaen_US
dc.contributor.authorLochner, Amandaen_US
dc.date.accessioned2017-05-03T15:31:40Z
dc.date.available2017-05-03T15:31:40Z
dc.date.issued2005en_US
dc.date.modified2009-09-15T07:37:24Z
dc.identifier.issn03008428en_US
dc.identifier.doi10.1007/s00395-005-0528-5en_AU
dc.identifier.urihttp://hdl.handle.net/10072/25682
dc.description.abstractBackground The mechanisms for obesity induced myocardial remodelling and subsequent mechanical dysfunction are poorly understood. There is good evidence that angiotensin II and TNFa have strong growth promoting properties and are elevated with obesity. In addition, these two peptides may interact to exacerbate myocardial ischaemic/reperfusion injury. Hypothesis Obesity increases systemic and myocardial renin-angiotensin system (RAS) activity and TNFa levels and contributes to obesity induced cardiac remodelling and ischaemic/reperfusion injury. Methods Male Wistar rats were placed on a standard rat chow diet or cafeteria diet for 16 weeks. Two additional groups of rats received the respective diets and losartan (30 mg/ kg/d) in their drinking water. Hearts were perfused on the isolated working rat heart perfusion system and mechanical function was documented before and after 15 min normothermic total global ischaemia. Blood and myocardial samples were collected for angiotensin II, TNFa and NADPH oxidase activity determinations. Results The rats on the cafeteria diet became obese compared to rats on the standard rat chow (438 ᠵ.9 g vs 393 ᠷ.3 g for control, p < 0.05). Obesity was associated with elevated serum angiotensin II (0.050 ᠰ.015 pmol/ml vs. 0.035 ᠰ.003 pmol/ml, p < 0.05) and TNFa levels (42.8 ᠵ.93 pg/ml vs. 13.18 ᠲ.50 pg/ml, p < 0.05), and increased heart to body weight ratios (3.1 ᠰ.04 mg/g vs. 2.8 ᠰ.03 mg/g, p < 0.05). Losartan had no effect on body weight but decreased basal myocardial angiotensin II and TNF? levels as well as heart to body weight ratio in the obese and lean controls (2.5 ᠰ.05 mg/g and 2.6 ᠰ.04 mg/g relative to their controls, p < 0.05). Hearts from obese rats had lower reperfusion aortic outputs (AO) than their concurrent controls (18.42 ᠱ.17 ml/min vs. 27.8 ᠰ.83 ml/min, p < 0.05). Losartan improved aortic output recoveries in obese rats (23.0 ᠱ.71 ml/min, p < 0.05). Conclusions Obesity increased serum angiotensin II and TNFa levels, blood pressure, and heart weight to body weight ratios. These changes were associated with decreased basal and post-ischaemic myocardial mechanical function. Chronic AT1 receptor antagonism prevented the adverse changes in heart weight, mechanical function and susceptibility to ischaemic/reperfusion injury. Although current data do not exclude additional mechanisms for obesity induced cardiac remodelling, they suggest that angiotensin II may contribute to obesity induced cardiac remodelling and ischaemic/reperfusion injury.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherDr Dietrich Steinkopff Verlagen_US
dc.publisher.placeHeidelberg, Germanyen_US
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom346en_US
dc.relation.ispartofpageto354en_US
dc.relation.ispartofissue4en_US
dc.relation.ispartofjournalBasic Research in Cardiologyen_US
dc.relation.ispartofvolume100en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchCardiology (incl. Cardiovascular Diseases)en_US
dc.subject.fieldofresearchcode110201en_US
dc.titleA potential role for Angiotensin II in obesity induced cardiac hypertrophy and ischaemic/reperfusion injuryen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2005
gro.hasfulltextNo Full Text


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