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The effect of angiotensin II recepto...
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Pourdjabbar, Ali.
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The effect of angiotensin II receptor blockade, prior to, during and after a myocardial infarction in rats with and without insulin resistance.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
The effect of angiotensin II receptor blockade, prior to, during and after a myocardial infarction in rats with and without insulin resistance./
作者:
Pourdjabbar, Ali.
面頁冊數:
169 p.
附註:
Source: Masters Abstracts International, Volume: 44-01, page: 0230.
Contained By:
Masters Abstracts International44-01.
標題:
Biology, Animal Physiology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=MR02533
ISBN:
9780494025338
The effect of angiotensin II receptor blockade, prior to, during and after a myocardial infarction in rats with and without insulin resistance.
Pourdjabbar, Ali.
The effect of angiotensin II receptor blockade, prior to, during and after a myocardial infarction in rats with and without insulin resistance.
- 169 p.
Source: Masters Abstracts International, Volume: 44-01, page: 0230.
Thesis (M.Sc.)--University of Toronto (Canada), 2005.
Since diabetes and myocardial infarction (MI) are associated with an up-regulation of the renin-angiotensin system (RAS), we hypothesized that Angiotensin-II receptor blockers will be beneficial in the peri- and post-large-MI periods, in Wistar and insulin-resistant rats (ZFR).
ISBN: 9780494025338Subjects--Topical Terms:
1017835
Biology, Animal Physiology.
The effect of angiotensin II receptor blockade, prior to, during and after a myocardial infarction in rats with and without insulin resistance.
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169 p.
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Source: Masters Abstracts International, Volume: 44-01, page: 0230.
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Thesis (M.Sc.)--University of Toronto (Canada), 2005.
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Since diabetes and myocardial infarction (MI) are associated with an up-regulation of the renin-angiotensin system (RAS), we hypothesized that Angiotensin-II receptor blockers will be beneficial in the peri- and post-large-MI periods, in Wistar and insulin-resistant rats (ZFR).
520
$a
In Wistar rats, Losartan at a high-dose (30mg/kg/day) caused significant hypotension resulting in increased 24hour mortality. In the 24hour post-MI survivors, Losartan administered progressively (3mg/kg/day progressively increased to 30mg/kg/day), reduced mortality between day-1 and day-38, improved ventricular remodeling, hemodynamics and fetal-gene expression profiles. In ZFR, Losartan administered progressively reduced early ventricular arrhythmias resulting in improved survival. Chronically, Losartan reduced cardiac hypertrophy and fetal-gene re-expression, however it did not improve ventricular remodeling and hemodynamics.
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These results indicate that the peri- and post-MI blockade of the RAS reduces arrhythmias and improves peri-MI survival only in the ZFR, while the chronic treatment improved the 24hour-38day survival, ventricular function and remodeling, fetal-gene and GLUT-4 mRNA expression in normal animals.
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