High-salt diet combined with elevated angiotensin II accelerates atherosclerosis in apolipoprotein E-deficient mice
Autor: | Peter Bie, Evelina Bernberg, Li-Ming Gan, Göran Bergström, Ole Skøtt, Irene J. Andersson, Maria E. Johansson |
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Rok vydání: | 2009 |
Předmět: |
Apolipoprotein E
medicine.medical_specialty Isoprostane Apolipoprotein B Physiology Aorta Thoracic Peptide hormone medicine.disease_cause Receptor Angiotensin Type 1 Article chemistry.chemical_compound Mice Apolipoproteins E Internal medicine Renin–angiotensin system Internal Medicine medicine Animals Salt intake Sodium Chloride Dietary Brachiocephalic Trunk biology business.industry Angiotensin II Atherosclerosis Lipids Oxidative Stress Endocrinology chemistry biology.protein Female Cardiology and Cardiovascular Medicine business Oxidative stress |
Zdroj: | Johansson, M E, Bernberg, E, Andersson, I J, Bie, P, Skøtt, O, Gan, L & Bergström, G 2009, ' High-salt diet combined with elevated angiotensin II accelerates atherosclerosis in apolipoprotein E-deficient mice ', Journal of Hypertension, vol. 27, no. 1, pp. 41-7 . |
ISSN: | 0263-6352 |
Popis: | OBJECTIVES: High-salt diet likely elevates blood pressure (BP), thus increasing the risk of cardiovascular events. We hypothesized that a high-salt diet plays a critical role in subjects whose renin-angiotensin systems cannot adjust to variable salt intake, rendering them more susceptible to atherosclerosis. METHODS: Apolipoprotein E-deficient (ApoE-/-) mice received standard or high-salt diet (8%) alone or in combination with fixed angiotensin II (Ang II) infusion (0.5 microg/kg per min). BP was measured using telemetry, and plaque burden was assessed in the thoracic aorta and innominate artery. We used urinary isoprostane as a marker for oxidative stress. RESULTS: Although high-salt diet per se did not affect plaque extension, high salt combined with Ang II increased plaque area significantly in both the aorta and the innominate artery as compared with Ang II or salt alone (P < 0.05 and P < 0.01, respectively). High-salt diet did not affect BP or isoprostane levels, whereas Ang II infusion increased both BP and isoprostane levels (P < 0.05 and P < 0.01, respectively). Although high-salt diet combined with Ang II did not amplify BP, salt in combination with Ang II increased isoprostane levels further (P < 0.001 vs. Ang II alone). Ang II increases macrophage content in lesions (P < 0.05), whereas salt likely increases collagen content. CONCLUSION: High-salt diet per se does not influence BP in ApoE-/- mice and is only moderately atherogenic. Possibly mediated via increased oxidative stress, a high-salt diet combined with fixed high Ang II levels accelerates atherogenesis synergistically, beyond the effect of BP. |
Databáze: | OpenAIRE |
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