Why the study?
Does preincubation with S-nitrosoglutathione, sodium nitroprusside, or prostaglandin E1 reduce thrombin-induced intracellular calcium rise and alkalization in human platelets?
Does preincubation with S-nitrosoglutathione, sodium nitroprusside, or prostaglandin E1 reduce thrombin-induced intracellular calcium rise and alkalization in human platelets?
S-nitrosoglutathione, sodium nitroprusside, and prostaglandin E1 inhibit both the intracellular calcium rise and the alkalizing response induced by thrombin in human platelets.
No immediate clinical implications; hypothesis-generating for S-nitrosoglutathione effects on platelet signaling.
S-Nitrosoglutathione and sodium nitroprusside, two activators of the soluble guanylate cyclase, inhibit the intracellular calcium rise evoked by thrombin at an early step of the activation cascade. A similar effect is obtained with prostaglandin E1, a drug that increases cAMP. We have found that in human platelets thrombin 0.1 IU/ml (approximately 1 nmol/l) produced a transient increase of [Ca2+]i. After a 10-min preincubation at 37 degrees C in 100 mumol/l S-nitrosoglutathione the peak value was reduced by 79 +/- 4% (mean and SEM, percentage of the parallel control). The [Ca2+]i peak was reduced by 66 +/- 4% after preincubation in 100 mumol/l sodium nitroprusside, and by 90 +/- 2% after preincubation in 10 mumol/l prostaglandin E1. Thrombin has a slow alkalizing effect. After a 10-min preincubation at 37 degrees C in 100 mumol/l S-nitrosoglutathione the change in pHi produced by thrombin was reduced by 35 +/- 5%, but only 12 +/- 4% after preincubation in 100 mumol/l sodium nitroprusside. The alkalizing effect of thrombin was also blunted by 10 mumol/l prostaglandin E1: the change of intracellular pH was decreased by 39 +/- 5%. As a conclusion, these drugs in addition to the reduction of rise in [Ca2+]i have an inhibitory effect on the alkalizing response induced by thrombin.
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Oscar A. Gende (2000) studied this question.
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