The angiotensin II AT1 receptor antagonist candesartan at antihypertensive plasma concentrations reduces damage induced by ischemia-reperfusion

被引:10
|
作者
Shimizu, M [1 ]
Wang, QD [1 ]
Sjöquist, PO [1 ]
Rydén, L [1 ]
机构
[1] Karolinska Hosp, Dept Cardiol, S-17176 Stockholm, Sweden
关键词
myocardial ischemia; reperfusion; angiotensin II; AT1-receptor antagonism; pig;
D O I
10.1023/A:1007763618021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to investigate if the angiotensin II AT1 receptor antagonist candesartan in antihypertensive plasma concentrations improves myocardial function and limits infarct size in anesthetized pigs. Animals were subjected to 45 min of regional ischemia and 240 min of reperfusion. Starting 60 min before ischemia, two groups of pigs (n = 6 in each) received either candesartan (25 mu g/kg bolus followed by a continuous infusion at a rate of 14 mu g/kg/h) or the corresponding volume of vehicle throughout the study period. Left ventricular systolic segment shortening (%SS) was measured by sonomicrometry, and infarct size was determined by triphenyl tetrazolium chloride staining. The plasma concentration of candesartan during the experiment was between 100 and 150 nmol/L, which was considered to be within the therapeutic range. Neither candesartan nor vehicle affected hemodynamics or coronary blood flow prior to ischemia. Compared to vehicle, candesartan improved recovery of %SS in the ischemic area. At 240 min of reperfusion, the %SS was significantly higher in pigs given candesartan than in pigs given vehicle (7.1 +/- 0.87% vs - 1 +/- 1.79%; p < 0.01). In both groups the area at risk was approximately 20 % of the left ventricle. Infarct size as a percentage of the area at risk was significantly smaller in the candesartan group than in the vehicle group (46 +/- 3.0 vs 73 +/- 3.6%; p < 0.01). The results suggest that angiotensin II AT1 receptor blockade, obtained in antihypertensive plasma concentrations, supports myocardial functional recovery and limits infarct size.
引用
收藏
页码:347 / 353
页数:7
相关论文
共 50 条
  • [1] The Angiotensin II AT1 Receptor Antagonist Candesartan at Antihypertensive Plasma Concentrations Reduces Damage Induced by Ischemia–Reperfusion
    Masafumi Shimizu
    Qing-Dong Wang
    Per-Ove Sjöquist
    Lars Rydén
    Cardiovascular Drugs and Therapy, 1999, 13 : 347 - 354
  • [3] Effects of the insurmountable angiotensin AT1 receptor antagonist candesartan and the surmountable antagonist losartan on ischemia/reperfusion injury in rat hearts
    Wang, QD
    Sjöquist, PO
    EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 380 (01) : 13 - 21
  • [4] Influence of the angiotensin II AT1 receptor antagonist irbesartan on ischemia/reperfusion injury in the dog heart
    Benedikt Preckel
    Wolfgang Schlack
    Michael Gonzàlez
    Detlef Obal
    Holger Barthel
    Volker Thämer
    Basic Research in Cardiology, 2000, 95 : 404 - 412
  • [5] TCV-116, an angiotensin II type 1 receptor antagonist, reduces hepatic ischemia-reperfusion injury in rats
    Araya, J
    Tsuruma, T
    Hirata, K
    Yagihashi, A
    Watanabe, N
    TRANSPLANTATION, 2002, 73 (04) : 529 - 534
  • [7] Chronic peripheral administration of the angiotensin II AT1 receptor antagonist Candesartan blocks brain AT1 receptors
    Nishimura, Y
    Ito, T
    Hoe, KL
    Saavedra, JM
    BRAIN RESEARCH, 2000, 871 (01) : 29 - 38
  • [8] Effects of captopril and angiotensin II receptor blockers (AT1, AT2) on myocardial ischemia-reperfusion induced infarct size
    Parlakpinar, Hakan
    Ozer, Mehmet Kaya
    Acet, Ahmet
    CYTOKINE, 2011, 56 (03) : 688 - 694
  • [9] An angiotensin II type 1 receptor blocker, candesartan, increases myocardial apoptosis in rats with acute ischemia-reperfusion
    Chen, M
    Hamada, M
    Hiasa, G
    Suzuki, M
    Ikeda, S
    Hiwada, K
    HYPERTENSION RESEARCH, 2001, 24 (03) : 323 - 329
  • [10] Pharmacological evaluation on antihypertensive activity of a novel AT1 angiotensin II receptor antagonist
    Tang, Bei
    Li, Helin
    Zhong, Ze
    Wu, Huiping
    Shen, Hongwei
    Hu, Jiayuan
    Ma, Jianping
    Wu, Jinting
    Wang, Yuehui
    CURRENT SCIENCE, 2019, 116 (12): : 1987 - 1992