AI Article Synopsis

  • A study investigated the effects of losartan pretreatment over varying durations (1 day, 1 week, and 4 weeks) on rats subjected to ischemia-reperfusion, finding significant cardiovascular protective benefits after 4 weeks.
  • After one and one week of losartan treatment, myocardial infarct size remained unchanged, but 4 weeks of treatment reduced infarct size significantly and improved endothelial-dependent vasorelaxation.
  • Additionally, losartan pretreatment was associated with decreased levels of vascular endothelial growth factor (VEGF) in ischemic myocardium, indicating an improvement in ischemia-related conditions.

Article Abstract

A previous study by our group showed that 10 weeks of pretreatment with losartan reduced myocardial infarct size and arrhythmias in a rat model of ischaemia-reperfusion. However, the effect of a differing time course of pretreatment has not been investigated. 104 Sprague-Dawley rats were randomised to four groups: a control, and three treatment groups in which losartan (40 mg/kg/day) was administered in drinking water for one day, one week, and four weeks respectively. After different durations of pretreatment, the rats were subjected to 17 minutes of left coronary artery occlusion and 120 minutes of reperfusion. Haemodynamic variables were not significantly different between the four groups. Myocardial infarct size was unchanged after one day and one week of pretreatment (52+/-7, 57+/-6% vs.control 55+/-3%), but was significantly reduced by four weeks of pretreatment with losartan (38+/-6, p<0.05). Endothelial-dependent vasorelaxation was significantly increased by four weeks of pretreatment (-81+/-4 vs.-62+7%, p<0.05). As an indicator of ischaemia, vascular endothelial growth factor (VEGF) levels in ischaemic myocardium were decreased after one and four weeks of pretreatment (0.75+/-0.05, 0.58+/-0.10 vs. 1.0, p<0.05,0.01, respectively). In conclusion, losartan has time-dependent cardiovascular protective effects. Four weeks of pretreatment with losartan decreased infarct size and VEGF, and improved endothelial dysfunction.

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Source
http://dx.doi.org/10.3317/jraas.2001.014DOI Listing

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