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Updated: May 17, 2026

Platelet Adhesion and Aggregation Under Flow using Microfluidic Flow Cells
Published on: October 27, 2009
Glycine reduces platelet aggregation
Peter Schemmer1, Zhi Zhong, Uwe Galli
1Department of General and Transplant Surgery, Ruprecht-Karls-University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany. Peter.Schemmer@med.uni-heidelberg.de
Dietary glycine significantly prolonged bleeding time and inhibited platelet aggregation in rats and humans. Glycine acts through glycine receptors to prevent platelet aggregation, offering potential therapeutic benefits.
Area of Science:
- Pharmacology
- Hematology
- Neuroscience
Background:
- Glycine-gated chloride channels are present in various immune cells, including macrophages and neutrophils.
- Glycine binding to its receptor causes chloride influx, leading to membrane hyperpolarization and preventing calcium influx.
- Platelet aggregation is a calcium-dependent process crucial for hemostasis.
Purpose of the Study:
- To investigate the hypothesis that glycine inhibits platelet aggregation.
- To determine the role of glycine receptors in this inhibitory effect.
- To assess the effect of dietary glycine on bleeding time and platelet aggregation.
Main Methods:
- Rats were fed diets supplemented with glycine or valine for five days.
- Bleeding time and platelet aggregation induced by ADP and collagen were measured.
- Glycine was added in vitro to assess its direct effect on platelet aggregation, with and without strychnine (a glycine receptor antagonist).
- Western blotting was used to detect glycine receptors in rat and human platelets.
Main Results:
- Dietary glycine significantly increased bleeding time twofold compared to controls.
- Platelet aggregation induced by ADP or collagen was reduced by over 50% in rats fed glycine.
- In vitro glycine addition dose-dependently inhibited rat platelet aggregation.
- Strychnine abolished the inhibitory effect of glycine in vitro, indicating a role for glycine receptors.
- Glycine also inhibited human platelet aggregation, and glycine receptors were detected in both rat and human platelets.
Conclusions:
- Glycine effectively prevents platelet aggregation in a dose-dependent manner.
- This effect is mediated through glycine receptors present on platelets.
- Glycine holds potential for therapeutic applications in conditions involving excessive platelet aggregation.
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