Abstract��OBJECTIVE To explore the protective effect of ginkgo-diyidamolum injection on rat myocardial cells injured by oxygen-glucose deprivation. METHODS The model of oxygen-glucose deprivation in rat myocardial cells was established. The cells were randomly divided into five groups:normal group, oxygen-glucose deprivation group, different ginkgo-diyidamolum injection dosage groups(0.28, 0.84, 1.40 mg��mL-1). The effects of ginkgo-diyidamolum injection on NO level, malondialdehyde (MDA) level, changes in the concentrations of lactate dehydrogenase (LDH), superoxide dismutase (SOD) activity were evaluated. Cells apoptosis rate was determined by flow cytometry. The gene transcription level of myocardial cell gap junction protein 43 (Cx43) was monitored by RT-PCR. RESULTS Compared with oxygen-glucose deprivation group, ginkgo-diyidamolum injection could reduce the content of intracellular NO, MDA, LDH and enhance the activity of SOD. Ginkgo-diyidamolum injection high dose and middle dose groups obviously improved the myocardial cell morphology, inhibited cell apoptosis and Cx43 gene in myocardial cells. CONCLUSION Ginkgo-diyidamolum injection has a strong protective effect when myocardial cells injured by oxygen-glucose deprivation, which is related to the antioxidant effect, inhibition of cell apoptosis, and maintaining the role of myocardial gap junction channel.
SUN N, XU G, ZHANG F, et al. Study on protective effect of Sijunzi decoction(red/white ginseng) on H2O2-induced H9c2 cardiomyocytes apoptosis[J]. China J Chin Mater Med(�й���ҩ��־),2015,3(10):1989-1993.
[2]
WU H X, WANG W G, ZHAO B,et al. Association between heart failure classification and sinus rhythm oscillation in ischemic cardiomyopathy[J]. Med J Chin People Arm Police Force(�侯ҽѧ),2015,26(1):68-71.
[3]
BIN C. Research of pharmacological action and clinical application of Ginkgo Dipyridamole Injection[J]. China Pharm(�й�ҩҵ), 2010,19(14):88-90.
[4]
ZHA Y, LI L. Systematic evaluation of yinxing damo injection in the treatment of angina pectoris[J]. J China Pharm(�й�ҩ��),2010,21(44):4143-4147.
[5]
ZHOU Q, HOU D B. Pharmacological and adverse effects of ginkgo dipyridamole injection[J]. J China Pharm(�й�ҩ��),2013,24(28):2686-2688.
[6]
SIMPSON P, SAVION S. Differentiation of rat myocytes in single cell cultures with and without proliferating nonmyocardial cells[J]. Circ Res,1982,50(1):101-116.
[7]
LIU Q Y, ZHANG Y Y, WAN H T, et al. Study of compatibility of liquiritin,glycyrrhetinic acid and hypaconitine[J]. Chin Arch Tradit Chin Med(�л���ҽҩѧ��),2013,31(3):493-495.
[8]
LIU J M. Influence of the extract of ginkgo leaves on the cerebral vascular diameter and inflammatory reactants of patients with lacunar infarction[J]. Chin Comm Doct(�й�����ҽ��),2015,31(1):18-19.
[9]
YE L, YU Y P, YAN M X,et al. Effects of Ginkgo biloba extract on the hepatic endoplasmic reticulum stress-related JNK pathway in rats with hepatic fibrosis[J]. China J Tradit Chin Med(�л���ҽҩ��־),2015,30(1):293-295.
[10]
YAO L Y, WANG J C, LIU J J, et al. Effect of Ginkgo biloba extract on vascular endothelial function in patients with type 2 diabetes mellitus[J]. Clin Focus,2014,29(1):88-89.
[11]
YAO X M. Experimental study on the effect of Ginkgo biloba extract on immunological hepatic fibrosis in rats induced by pig blood[J]. J Guangxi Med Univ(����ҽ�ƴ�ѧѧ��),2014,31(6):921-923.
[12]
QI Y X, ZHAO H P, ZHU Y Y. Pharmacological action and clinical application progress of dipyridamole[J]. J Taishan Med Coll(̩ɽҽѧԺѧ��),2005,26(4):124-129.
[13]
ZHANG W P, DENG Y Y, REN J X, et al. Mechanisms of total flavones of Epimedium on oxidative stress induced by myocardial ischemia / reperfusion injury in rats[J]. China J Chin Mater Med(�й���ҩ��־),2016,41(18):3400-3405.
[14]
LI Q, CHEN X, KAN X X, et al. Protective effect and mechanism of compound Ginkgo biloba granules on oxidative stress injury of HUVEC[J]. China J Chin Mater Med(�й���ҩ��־),2016,41(4):722-727.
[15]
ZOU C C, XU Q X, YAN H Y, et al. Antioxidant activity and protective effect of fructus trichosanthis extracts with different solvent on myocardial ischemia reperfusion injury in rats[J]. Chin Pharm J(�й�ҩѧ��־),2017,52(2):124-129.
[16]
RAJNAI H, TELEKI I, KISZNER G, et al. Connexin 43 communication channels in follicular dendritic cell development and in follicular lymphomas[J]. J Immunol Res, 2015,2015:528098.
[17]
ZHANG W, SONG J K, DU G H. Apoptosis signal transduction pathways in ischemia-reperfusion injury[J]. Chin Pharm J(�й�ҩѧ��־), 2015,50(7):565-569.