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Biomedical subjects

J J Sun

Publications and source records attributed to J J Sun.

30 records · Page 2Linked to original sources
PubMed1990

[Protective effects of Panax notoginseng saponins on experimental myocardial injury induced by ischemia and reperfusion in rat].

Effects of total saponins of Panax notoginseng (PNS) and purified ginsenosides Rb1 and Rg1 from PNS on myocardial injury induced by cardiac ischemia and reperfusion were studied with rat hearts in situ and in vitro. In pentobarbital-anesthetized rats, PNS pretreatment (100 and 200 mg/kg) provided significant reduction in myocardial infarct size after left descending coronary artery ligation (40 min) and reperfusion (120 min) in comparison with the control. PNS 12.5 and 25 mg/L, Rb1 10 mg/L, and Rg1 10 mg/L significantly decreased cardiac CPK release, attenuated myocardial Ca2+ accumulation, reduced malondialdehyde (MDA) production and prevented reduction of superoxide dismutase (SOD) activity in comparison with the control in perfused isolated rat hearts with global ischemia (40 min) and reperfusion (15 min). The results show that PNS, Rb1, and Rg1 prevent cardiac ischemia and the action is considered to be related to the inhibition of lipid peroxidation.

Animals↗
PubMed1989

[Effects of Panax notoginseng saponin Rb1 and Rg1 on myocardial action potential and slow inward current].

The effects of Rb1, Rg1 (purified saponin of Panax notoginseng) on contraction force, action potential and slow inward current of guinea pig papillary muscles were studied by intracellular microelectrodes and voltage clamp techniques. The contraction force was decreased and the APD20 was shortened in the presence of Rb1 1 mg/ml, while the RP, APA and Vmax remained unchanged. The amplitude of Isi was decreased from a peak value of 9.8 +/- 1.6 to 7.3 +/- 3.4 microA after 20 min perfusion with Rb1 solution. This effect was reversed by increasing calcium concentration. Rg1 1 mg/ml decreased the contraction force significantly without affecting the configuration of action potential and the amplitude of slow inward current. The results indicate that Rb1 has a blocking effect on calcium channels, but Rg1 has not.

Action Potentials↗
PubMed1989

[Effects of Panax notoginseng saponins on cardiac action potentials and slow inward current].

The effects of total saponins of Panax notoginseng (PNS) on contraction force, normal and slow response action potentials and slow inward current of guinea pig papillary muscles were studied by intracellular microelectrodes and voltage clamp techniques. The contraction force was decreased and the APD20, APD90 of normal AP were shortened in the presence of PNS 1 mg/ml, while the RP, APA and Vmax remained unchanged. The APA of slow AP induced with high K+ was decreased to 85% of its normal value after 20 min of perfusion with PNS solution. Isi was decreased from a peak value of 9.8 +/- 2.0 to effects of PNS on slow affecting INa. The 6.9 +/- 3.6 microA without AP and Isi were reversed by increasing calcium concentration. The results indicate that PNS has a selective blocking effect on calcium channels.

Action Potentials↗
PubMed1987

[Influence of cell-cell interaction upon differentiation of murine embryonal carcinoma cells].

Embryonal carcinoma (EC) cells are the pluripotent stem cells of teratocarcinoma. The aggregates of P19, a mouse EC cell line, undergo differentiation and rapidly lose its colony-forming ability in culture with retinoic acid (RA) or DMSO. Loss of plating efficiency is used to assess the rate of drug-induced differentiation. When exposed respectively to DMSO or RA, the isolated EC cell mutants (D3 and RAC65) did not differentiate but the gap junctions could be formed. In RA-treated co-aggregates of RAC65 and O1A1, each cell line gave responses independent of the presence of the other cell line. However, in DMSO-treated co-aggregates of P19 and D3, D3 cells remained undifferentiated and P19 cell differentiation was much poorer than that in the absence of D3 cells. The results suggest that cell-cell interaction be present in the early stage of DMSO-induced differentiation and absent in the early stage of RA-induced differentiation.

Animals↗
PubMed1986

Actions of cardiotoxins from the southern Chinese cobra (Naja naja atra) on rat cardiac tissue.

The cardiotoxic actions of southern Chinese cobra (Naja naja atra) venom have been investigated. Cardiotoxicity accounted for lethality of crude venom in anaesthetized rats and cardiotoxic polypeptides constituted the bulk of the venom when it was fractionated by CM-Sephadex chromatography. The cardiotoxic actions of these polypeptides were investigated in isolated cardiac tissue. Actions of cardiotoxins on rate, force and intracellular potentials occurred more readily in ventricular tissue and were reversible in all cardiac tissues. Bolus injections of cardiotoxins to perfused rat hearts produced profound changes in intracellular potentials, but such changes were reversed by 10 min after toxin wash-out. The changes included depolarization and loss of the fast phase (0) of the action potential. The loss of beating and contracture produced by cardiotoxins in isolated atria and ventricles showed such marked tachyphylaxis that toxicity was lost after 2-5 exposures. Both calcium and heparin ameliorated the cardiotoxic actions of cardiotoxins. Since the actions of cardiotoxin were partially selective for ventricular tissue, reversible, demonstrated tachyphylaxis and could be prevented, it is suggested that a specific molecular mechanism may be involved, rather than a non-specific action such as cell membrane destruction.

Animals↗
PubMed1985

Cell-cell interaction can influence drug-induced differentiation of murine embryonal carcinoma cells.

When cultured in the presence of either retinoic acid (RA) or dimethyl sulfoxide (DMSO), aggregates of the P19 line of mouse embryonal carcinoma (EC) cells differentiate and the spectrum of cell types formed depends on the drug dose. It is shown here the EC cells rapidly lose their colony-forming ability when cultured as aggregates in the presence of DMSO. This loss of plating efficiency (PE) also occurs rapidly following RA treatment. Loss of PE has been used as a quantitative procedure for assessing the rate of drug-induced differentiation. The relationship between drug dose and loss of PE is much steeper for DMSO than for RA, suggesting that these two drugs affect different stages of the differentiation decision-making apparatus. Mutant EC cell lines (D3 and RAC65) do not differentiate in the presence of drug-inducers (DMSO and RA, respectively). Neither differentiation-deficient mutant has an altered ability to form gap junctions. When D3 and P19 cells were mixed within the same DMSO-treated aggregates, the D3 cells remained undifferentiated and the P19 cells differentiated much less efficiently than if they were cultured in the absence of the D3 cells. When RAC65 and P19 cells were mixed in RA-treated aggregates, each cell responded to the drug as though the other were absent. Thus RA behaves as a cell-autonomous inducer of differentiation, whereas DMSO-induced differentiation seems to be mediated by interactions between neighboring cells.

Animals↗
PubMed1985

Commitment in a murine embryonal carcinoma cell line during differentiation induced by retinoic acid.

Murine embryonal carcinoma (EC) cells are induced to differentiate when cultured in the presence of retinoic acid (RA). Whereas the EC cells have a high plating efficiency, the differentiated cells have little or no colony-forming ability under the same conditions. We have assumed that the loss of colony-forming ability following exposure of EC cells to RA corresponds to the irreversible commitment of EC cells to differentiate. We found that uncommitted EC cells persist in RA-treated aggregates of EC cells and that the proportion of EC cells stabilizes at a level inversely related to the RA concentration. Both experimental evidence and mathematical modelling results are consistent with the interpretation that there is a dynamic equilibrium achieved by a balance between the processes of EC cell proliferation and differentiation. Since different cell types are induced by different RA concentrations, our results suggest that the commitment to differentiate is not related in any simple way to the developmental program which ensues.

Animals↗