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Xiyuan Hospital, China Academy of Chinese Medical Sciences,Beijing,China
纸质出版日期:2015,
网络出版日期:2014-7-14,
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Guo, Cy., Ma, Xj., Wang, Js. et al. Effects of Panax Quinquefolium Saponin on phosphatidylinositol 3-kinase/serine threonine kinase pathway of neonatal rat myocardial cells subjected to hypoxia., Chin. J. Integr. Med. 21, 384–388 (2015). https://doi.org/10.1007/s11655-014-1881-8
Chun-yu Guo, Xiao-juan Ma, Jing-shang Wang, et al. Effects of Panax Quinquefolium Saponin on phosphatidylinositol 3-kinase/serine threonine kinase pathway of neonatal rat myocardial cells subjected to hypoxia[J]. Chinese Journal of Integrative Medicine, 2015,21(5):384-388.
Guo, Cy., Ma, Xj., Wang, Js. et al. Effects of Panax Quinquefolium Saponin on phosphatidylinositol 3-kinase/serine threonine kinase pathway of neonatal rat myocardial cells subjected to hypoxia., Chin. J. Integr. Med. 21, 384–388 (2015). https://doi.org/10.1007/s11655-014-1881-8 DOI:
Chun-yu Guo, Xiao-juan Ma, Jing-shang Wang, et al. Effects of Panax Quinquefolium Saponin on phosphatidylinositol 3-kinase/serine threonine kinase pathway of neonatal rat myocardial cells subjected to hypoxia[J]. Chinese Journal of Integrative Medicine, 2015,21(5):384-388. DOI: 10.1007/s11655-014-1881-8.
To explore the effects of Panax Quinquefolium Saponin (PQS) on phosphatidylinositol 3-kinase/serine threonine kinase (PI3K/Akt) pathway of neonatal rat myocardial cells subjected to hypoxia. Neonatal rat myocardial cells were cultured in vitro. After the myocardial cell injury was induced by hypoxia
the cells were randomized into 5 groups: the normal group
the model group
the positive control group (Ciclosporin A
2 µ mol/L)
the low-dose PQS group (PQSL
25mg/L)
and the high-dose PQS group (PQSH
50 mg/L). Morphology and behavior of myocardial cells were observed under an inverted microscope. Apoptosis rate and lactate dehydrogenase (LDH) leakage rate of myocardial cells were determined by colorimetry. Mitochondrial transmembrane potential was assessed using a fluorexon laser. Phospho-glycogen synthase kinase (GSK)-3β and phospho-Akt as well as cytochrome C were determined by Western blot LDH leakage in the Ciclosporin A group
PQSH group and PQSL group reduced progressively compared with the model group (P<0.05). Akt and GSK-3β was strongly phosphorylated after treatment with Ciclosporin A and PQS compared with the model group (P<0.05
P<0.01). Compared with the model group (16.41±1.74; 35.28±6.30)
both the integrated optical density of mitochondrial permeability transition pore (MPTP) and the mitochondrial transmembrane potential significantly increased in the PQSH group (42.74±2.12; 71.36±6.54) and the PQSL group (39.58±1.49; 66.99±5.45; P<0.05
P<0.01). However
the protein of cytochrome C outside the mitochondrion decreased in the PQSH group (273.66±14.61) and the PQSL group (259.62±17.31) compared with the model group (502.41±17.76; P<0.05). Through activation of the PI3K/Akt pathway and inhibition of the MPTP
PQS might protect the heart against ischemia injury and apoptosis of myocardial cells.
To explore the effects of Panax Quinquefolium Saponin (PQS) on phosphatidylinositol 3-kinase/serine threonine kinase (PI3K/Akt) pathway of neonatal rat myocardial cells subjected to hypoxia. Neonatal rat myocardial cells were cultured in vitro. After the myocardial cell injury was induced by hypoxia
the cells were randomized into 5 groups: the normal group
the model group
the positive control group (Ciclosporin A
2 µ mol/L)
the low-dose PQS group (PQSL
25mg/L)
and the high-dose PQS group (PQSH
50 mg/L). Morphology and behavior of myocardial cells were observed under an inverted microscope. Apoptosis rate and lactate dehydrogenase (LDH) leakage rate of myocardial cells were determined by colorimetry. Mitochondrial transmembrane potential was assessed using a fluorexon laser. Phospho-glycogen synthase kinase (GSK)-3β and phospho-Akt as well as cytochrome C were determined by Western blot LDH leakage in the Ciclosporin A group
PQSH group and PQSL group reduced progressively compared with the model group (P<0.05). Akt and GSK-3β was strongly phosphorylated after treatment with Ciclosporin A and PQS compared with the model group (P<0.05
P<0.01). Compared with the model group (16.41±1.74; 35.28±6.30)
both the integrated optical density of mitochondrial permeability transition pore (MPTP) and the mitochondrial transmembrane potential significantly increased in the PQSH group (42.74±2.12; 71.36±6.54) and the PQSL group (39.58±1.49; 66.99±5.45; P<0.05
P<0.01). However
the protein of cytochrome C outside the mitochondrion decreased in the PQSH group (273.66±14.61) and the PQSL group (259.62±17.31) compared with the model group (502.41±17.76; P<0.05). Through activation of the PI3K/Akt pathway and inhibition of the MPTP
PQS might protect the heart against ischemia injury and apoptosis of myocardial cells.
Panax Quinquefolium Saponinischemic cardiomyocytesphosphatidylinositol 3-kinase/serinethreonine kinasemitochondrial permeability transition pore
Panax Quinquefolium Saponinischemic cardiomyocytesphosphatidylinositol 3-kinase/serinethreonine kinasemitochondrial permeability transition pore
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