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Pretreatment of ginsenoside-Rd reduces ischemia-reperfusion injury in isolated rat hearts by increasing coronary flow
SONG Chun 1 #,WANG Liping 1,WANG Qilong 1,GAO Mingtang 2 *
1.School of Basic Medical Science, Lanzhou University, Lanzhou 730000
2.Key Laboratory of Preclinical Study for New Drugs of Gansu Province, Lanzhou 730000
*Correspondence author
#Submitted by
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Funding: none
Opened online:16 January 2012
Accepted by: none
Citation: SONG Chun,WANG Liping,WANG Qilong.Pretreatment of ginsenoside-Rd reduces ischemia-reperfusion injury in isolated rat hearts by increasing coronary flow[OL]. [16 January 2012] http://en.paper.edu.cn/en_releasepaper/content/4458840
 
 
Objective: To evaluate the myocardial effects of ginsenoside-Rd in isolated rat hearts and to investigate the potential protective mechanism of ischemia-reperfusion injury. Methods: All rat hearts were isolated and perfused with modified Krebs-Heinseleit buffer (KHB) using the Langendorff preparation. For ischemia-reperfusion trial groups, hearts were treated with ginsenoside-Rd for 10 minutes after 20 minutes’ equilibrium, followed by 30 minutes’ global ischemia and 120 minutes’ reperfusion. For working heart trial groups, hearts were perfused with KHB containing ginsenoside-Rd for 40 minutes after 20 minutes’ equilibrium. Both of these two randomized controlled trials were performed using verapamil as positive control. Coronary flow (CF), heart rate (HR), left ventricular end diastolic pressure (LVEDP), left ventricular systolic pressure (LVSP), left ventricular developed pressure (LVDP), and rate pressure product (RPP) were collected to analyze the myocardial effects of ginsenoside-Rd. Results: Ginsenoside-Rd significantly increased the CF in both I/R trial and working heart trial (P<0.05). In I/R trial, it also helped lower the LVEDP and increase the RPP (P<0.05). However, in working heart trial, it showed no significant difference on the HR and LVDP (P>0.05).Conclusion: Pretreatment of ginsenoside-Rd of a middle dose could play a protective role in isolated rat ischemia-reperfusion hearts, by increasing the coronary flow rather than influencing cardiac functional properties previously.
Keywords:Ischemia-reperfusion injury; Ginsenoside-Rd; Coronary flow
 
 
 

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