Related Experiment Video
Updated: Aug 7, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
The H1-histamine antagonist dithiaden inhibits human platelet function in vitro
The H-histamine receptor antagonist Dithaden inhibited in a dose-dependent manner, human platelet 1 aggregation in vitro that was induced with stimuli in the following rank order of potency: thrombin > A23187 > adrenaline > ADP. The aggregation of platelets in plasma induced with adrenaline was inhibited by Dithiaden (DIT) (both the first and the second phase) and the onset of the second phase was prolonged significantly. In a concentration-dependent manner DIT inhibited thrombin- and calcium ionophore A23187-induced {3H}arachidonic acid liberation from, and peroxidation (measured as malondialdehyde formation) of membrane phospholipids. The same effect of DIT was found for the inhibition of thromboxane B suggested that DIT does not inhibit stimulated platelets at specific histamine receptors sites but rather at the phospholipase A and thromboxane synthase level. Results from in vitro experiments should be verified in 2 vivo . generation. It is 2.
The H-histamine receptor antagonist Dithaden inhibited in a dose-dependent manner, human platelet 1 aggregation in vitro that was induced with stimuli in the following rank order of potency: thrombin > A23187 > adrenaline > ADP. The aggregation of platelets in plasma induced with adrenaline was inhibited by Dithiaden (DIT) (both the first and the second phase) and the onset of the second phase was prolonged significantly. In a concentration-dependent manner DIT inhibited thrombin- and calcium ionophore A23187-induced {3H}arachidonic acid liberation from, and peroxidation (measured as malondialdehyde formation) of membrane phospholipids. The same effect of DIT was found for the inhibition of thromboxane B suggested that DIT does not inhibit stimulated platelets at specific histamine receptors sites but rather at the phospholipase A and thromboxane synthase level. Results from in vitro experiments should be verified in 2 vivo . generation. It is 2.
More Related Videos
09:13Turbidimetry on Human Washed Platelets: The Effect of the Pannexin1-inhibitor Brilliant Blue FCF on Collagen-induced Aggregation
Published on: April 6, 2017
09:19In Vitro Microfluidic Disease Model to Study Whole Blood-Endothelial Interactions and Blood Clot Dynamics in Real-Time
Published on: May 24, 2020
Related Concept Videos
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Acid Suppressive Drugs for Peptic Ulcer Disease: Histamine H2-Receptor Antagonists