thromboxane-b2 has been researched along with tetrandrine* in 2 studies
2 other study(ies) available for thromboxane-b2 and tetrandrine
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Effects of tetrandrine and fangchinoline on human platelet aggregation and thromboxane B2 formation.
Tetrandrine (TET) and fangchinoline (FAN) are two major components of the radix of Stephania tetrandra. The effects of TET and FAN on human platelet aggregation and formation of thromboxane (TX) B2, a stable metabolite of TXA2, were examined in the aspect of platelet aggregation. TET and FAN inhibited platelet-activating factor (PAF)-induced human platelet aggregation. IC50 values for TET and FAN were 28.6+/-3.24 microM and 21.7+/-2.61 microM, respectively. In the PAF-receptor binding assay, neither TET nor FAN showed any inhibitory effects on the specific bindings of PAF to its receptor. TET and FAN also inhibited PAF-, thrombin- and arachidonic acid-induced thromboxane B2 formation in human washed platelet. These results indicate that TET and FAN inhibit the platelet aggregation by interfering with the intracellular messengers system, but not by inhibiting the binding of PAF to PAF-receptor on the platelet membrane directly, and the suppression of TXA2 formation by TET and FAN may be responsible for their inhibitory activities on the platelet aggregation and further on the thrombosis. Topics: Alkaloids; Benzylisoquinolines; Blood Platelets; Drugs, Chinese Herbal; Humans; In Vitro Techniques; Platelet Aggregation; Platelet Aggregation Inhibitors; Platelet Membrane Glycoproteins; Receptors, Cell Surface; Receptors, G-Protein-Coupled; Thromboxane B2 | 1999 |
Effects of tetrandrine on production of leukotriene B4 and thromboxane B2 in rabbit blood.
The effects of tetrandrine (Tet) on the production of 2 major metabolites of arachidonic acid (AA), the leukotriene B4 (LTB4) and the thromboxane B2 (TXB2) in rabbit whole blood were investigated by reversed phase high pressure liquid chromatography (HPLC) and radioimmunoassay (RIA), respectively. After incubation with different doses of Tet for 15 min in vitro, the production of LTB4 and TXB2 by rabbit whole blood stimulated with calcimycin (20 mumol.L-1) was inhibited in a dose-dependent manner, with IC50 value of 17.8 +/- 8.6 and 17.7 +/- 9.2 mumol.L-1, respectively. In the presence of exogenous AA, the inhibitory effects of Tet were markedly lessened. The effects of Tet were much like those of calmodulin (CaM) antagonist fluphenazine (Flu). Dexamethasone (Dex) also inhibited the production of LTB4 and TXB2 when incubated with rabbit whole blood for 60 min. Tet iv 10 mg.kg-1 also inhibited the production of LTB4 and TXB2 in rabbit whole blood stimulated with calcimycin. These results suggest that Tet may be an antagonist of CaM, thus suppressing the release of AA which was catalyzed by CaM dependent phospholipase A2 (PLA2) from the membrane phospholipids of blood cells. Topics: Alkaloids; Animals; Benzylisoquinolines; Calcimycin; Calcium Channel Blockers; Chromatography, High Pressure Liquid; Female; Leukotriene B4; Male; Rabbits; Radioimmunoassay; Thromboxane B2 | 1993 |