• English
    • Persian
  • English 
    • English
    • Persian
  • Login
View Item 
  •   KR-TBZMED Home
  • TBZMED Published Academics Works
  • Published Articles
  • View Item
  •   KR-TBZMED Home
  • TBZMED Published Academics Works
  • Published Articles
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Amlodipine treatment decreases plasma and carotid artery tissue levels of endothelin-1 in atherosclerotic rabbits

Thumbnail
Date
2011
Author
Rashidi, B
Mohammadi, M
Mirzaei, F
Badalzadeh, R
Reisi, P
Metadata
Show full item record
Abstract
Alteration in transferring of calcium ions are seen in atherosclerotic cells and amlodipine can positively influence risk factors associated with atherosclerosis, but all mechanisms are not known. Recent studies indicate that endothelin-1 (ET-1) contributes to the atheroma formation and progression of atherosclerosis. In this study, we have evaluated the effects of amlodipine treatment and/or high-cholesterol diet on blood and carotid artery tissue concentration of ET-1 in the atherosclerotic rabbits. Thirty six male New Zealand white rabbits were randomly divided into four groups: normal-diet control (NC), normal-diet receiving amlodipine (NA), high-cholesterol diet (HC) and high-cholesterol diet receiving amlodipine (HA) groups. After 8 weeks all animals were anesthetized and blood or carotid tissue samples were colleted. Eight weeks of amlodipine treatment reduced significantly total cholesterol, LDL and TG in hypercholesterolemic (HA) group. Significant increase in plasma HDL-C and decrease in TG were the main effects of amlodipine treatment on serum lipid profiles in the control group. The plasma and carotid tissue levels of ET-1 in HC group were significantly increased as compared with the NC group (p< 0.01). Amlodipine treatment significantly reduced ET-1 level in NA and HA rabbits (p< 0.01). Furthermore, high-cholesterol diet induced atherosclerotic lesions as shown by the enhancement of endothelial cell diameter and accumulation of lipid droplets under endothelial cells. Amlodipine treatment reduced atherotic lesions in these rabbits. Amlodipine treatment reduced levels of total cholesterol, LDL and TG as well as plasma and carotid tissue levels of ET-1 in high lipid situation. We suggest that amlodipine treatment by reducing the ET-1 may contribute to reducing the progression of atherosclerotic disease. é 2010 Elsevier Ireland Ltd.
URI
http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52476
Collections
  • Published Articles

Related items

Showing items related by title, author, creator and subject.

  • Evaluation of serum levels of lipids and lipoproteins in kidney-transplanted patients 

    Mortazavi, M; Tohidi, M; Rahbani-Nobar, M (2001)
    [No abstract available]
  • Correlation between leptin serum levels with lipid profile and anthropometric indices in women with different grades of obesity 

    Zarghami, N; Maleki, MJ; Mamaghani, F; Mohammadzadeh, G; Pourhassan, M (2010)
    Background and Objective: Leptin is a 16 KDa peptide which has a close correlation with adiposity. However, its effect on lipid profile is controversial in human. Therefore, this study was performed to investigate correlation ...
  • Association of S100B serum levels with metabolic syndrome and its components [Associaç?o dos n?veis de soro S100B com a s?ndrome metab?lica e seus componentes] 

    Kheirouri, S; Ebrahimi, E; Alizadeh, M (2018)
    Introduction: We aimed to compare serum levels of S100B between patients with metabolic syndrome and healthy subjects and to investigate the association of S100B with components of the metabolic syndrome. Materials and ...

Knowledge repository of Tabriz University of Medical Sciences using DSpace software copyright © 2018  HTMLMAP
Contact Us | Send Feedback
Theme by 
Atmire NV
 

 

Browse

All of KR-TBZMEDCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

My Account

LoginRegister

Knowledge repository of Tabriz University of Medical Sciences using DSpace software copyright © 2018  HTMLMAP
Contact Us | Send Feedback
Theme by 
Atmire NV