Protective Effects of Total Flavonoid from Mori Folium on Myocardial Ischemic-reperfused Injury in Rats
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Protective Effects of Total Flavonoid from Mori Folium on Myocardial Ischemic-reperfused Injury in Rats
Chinese Journal of Experimental Traditional Medical FormulaeVol. 17, Issue 19, Pages: 185-187(2011)
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Published:2011
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WANG Ping. Protective Effects of Total Flavonoid from Mori Folium on Myocardial Ischemic-reperfused Injury in Rats[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(19): 185-187.
DOI:
WANG Ping. Protective Effects of Total Flavonoid from Mori Folium on Myocardial Ischemic-reperfused Injury in Rats[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(19): 185-187.DOI:
Protective Effects of Total Flavonoid from Mori Folium on Myocardial Ischemic-reperfused Injury in Rats
Objective: To study effects of the total flavones from Mori Folium(TFMF)on myocardial cell apoptosis and caspase-3 expression in myocardial ischemic-reperfusion injury in rats. Method: Ninety SD rats were randomized into sham operation group
model group
three dose groups of TFMF(35
70
140 mg·kg-1·d-1)
Tonxinluo capsule group(100 mg·kg-1·d-1).The left anterior descending coronary artery was ligated for 30 min
followed by 2 h of reperfusion to establish the rat model of myocardial ischemia-reperfusion injury. myocardia apoptosis were detected by the TUNEL staining and caspase-3 expression was detected by immunohistochemical technique method. Result: IS/LV and IS/AR increased obviously in model group compared with those in sham group
Myocardial apoptosis rate increased obviously(P<0.01)and caspase-3 protein expression was significantly elevated(P<0.05 or P<0.01)in the model group. Compared with model group
IS/LV
IS/AR and myocardial apoptosis rate in TFMF group decreased obviously(P<0.05 or P<0.01)
and caspase-3 protein expression was down-regulated(P<0.05 or P<0.01). Conclusion: TFMF possessed an obviouse ameliorate effect on myocardial cell apoptosis in myocardial ischemic-reperfused injury rats by decreasing the caspase-3 protein expression.