XU Rong-rong, LI Ying-dong, LIU Kai, et al. Protection Effect of Ultra-filtration Extract from the Mixture of and on Adriamycin-induced Myocardial Apoptosis of Neonatal Rats[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(15): 222-226.
DOI:
XU Rong-rong, LI Ying-dong, LIU Kai, et al. Protection Effect of Ultra-filtration Extract from the Mixture of and on Adriamycin-induced Myocardial Apoptosis of Neonatal Rats[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(15): 222-226. DOI: 10.11653/syfj2013150222.
Protection Effect of Ultra-filtration Extract from the Mixture of and on Adriamycin-induced Myocardial Apoptosis of Neonatal Rats
Objective: To investi gate the influence of ultra-filtration extract from the mixture of Angelica sinensis and Hedysarum polybotrys(UFE-AH) on myocardial cell apoptosis induced by adriamycin(ADR) of neonatal rats. Method: Myocardial cells of neonatal rats born 1 to 2 days were primarily cultured by differential adherent method for 48 h at 37℃
5%CO2 incubator
adjusting the cell concentration to 1×106/mL
then randomly divided into five group:normal control group
adriamycin group
low-does
medium-does
and high-does UFE-AH.to detect MTT method was used to inhibition of cell growth rate
and to detect the level of de-oxyribonucleic acid damage (DNA damage) the single cell gel electrophoresis was used
western blot was used to detect the expression of Bcl-2 and Bax. Result: Compared with the normal group
the inhibition of cell growth rate in adriamycin group increased significantly
head DNA%(HDNA%)
tail DNA%(TDNA%)
tail length(TL)
tail moment(TM)
olive tail moment(OTM) were significantly increased
the protein expressions of Bcl-2 were decreased and the protein expressions of Bax were increased significantly (P<0.01);In comparison of the four other groups with model group
UFE-AH
HDNA%
TDNA%
TL
TM
OTM numerical and the protein expressions of Bax
but increase the protein expressions of Bcl-2 of the myocardial ceels in neonatal rats and the radio of Bcl-2/Bax. Conclusion: can reduce the DNA damage of the myocardial cells induced by adriamycin and increase the radio of Bcl-2/Bax
and has the protective effects on myocardial cell apoptosis induced by adriamycin of neonatal rats.