Responder lymphocytes were cultured with an equal number of irradiated
stimulator lymphocytes from another donor for 6 days in RPMI 1640 (a
modified Me Coh's 5 A Medium), After 48 h incubation with PMA (phorbol
12-myristate), PRA (phytohaematogglutin) and 120 h with MLR (mixed ly
mphocytes reaction), the cells were labelled with H-3-thymidine, Cells
were harvested in a scintillation counter, Globularia alypum L. extra
cts were dissolved in HPLC quality ethanol or water and diluted in RPM
I to concentrations ranging from 0.156-10 mu g/mL. Extract solutions w
ere added immediately after cell stimulation in the cell walls, Cyclos
porin A was used as a control. Both the water and ethanol extracts of
Globularia alypum L. demonstrated a dose response effect in all three
systems of MLR, PHA and PMA with no statistical difference in water or
ethanol extracts, The IC50 were: PHA 1.14 mu g/mL, PMA 1.05 mu g/mL a
nd MLR 2.06 mu g/mL. The PHA and MLR IC50 are approximately double the
IC50 for cyclosporin A (0.5 mu g/mL). The effects of Glubularia alypu
m L. in PMA stimulated lymphocytes suggests it may suppress T cell fun
ction through a pathway that cyclosporin A does not effect.