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Related Concept Videos

Extrinsic and Intrinsic Pathways of Hemostasis01:20

Extrinsic and Intrinsic Pathways of Hemostasis

Blood clotting or coagulation involves extrinsic and intrinsic pathways, which ultimately merge into the common pathway, forming a fibrin clot.
The Extrinsic Pathway
The extrinsic pathway of coagulation is typically initiated by tissue damage that exposes blood to tissue factor (TF), a protein released by the damaged tissue cells outside the blood vessels—this interaction with TF triggers biochemical reactions involving specific clotting factors. The key player here is Factor VII, which forms a...
Introduction to Hemostasis01:05

Introduction to Hemostasis

Hemostasis is a complex physiological process that prevents excessive bleeding when a blood vessel is injured. It's crucial for maintaining the integrity of the circulatory system, as it ensures that our blood remains fluid while still within the vascular network and yet clots to prevent blood loss upon vessel injury.
The three phases of hemostasis involve many clotting factors present in plasma and several substances released by platelets and injured tissue cells. It is a fast, localized, and...
Formation of the Platelet Plug01:22

Formation of the Platelet Plug

The platelet phase, the second stage of hemostasis, commences around 15-20 seconds after an injury. It follows and overlaps with the vascular phase, during which blood vessels constrict to minimize blood loss.
As the injured blood vessel contracts, endothelial cells undergo contraction, revealing collagen fibers in the basement membrane and underlying connective tissue. Furthermore, the plasma membrane of endothelial cells becomes adhesive, preparing the site for platelet adhesion. Platelets...
Clot Retraction and Fibrinolysis01:16

Clot Retraction and Fibrinolysis

After a fibrin clot is formed, the next step is clot retraction, a vital process facilitated by platelet contractile proteins, such as actin and myosin. These proteins pull the fibrin strands closer together and condense the clot. This action reduces the size of the clot, creating a smaller, denser structure that effectively seals off the damaged vessel. Clot retraction consolidates the clot and helps with wound healing by bringing the edges of the damaged blood vessel closer together.
Amplifying Signals via Enzymatic Cascade01:22

Amplifying Signals via Enzymatic Cascade

When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze the...
Vascular Spasm01:16

Vascular Spasm

The vascular phase, also known as vasospasm, is the initial stage of hemostasis, crucial for preventing excessive bleeding when a blood vessel is injured. After a vessel is cut, nerves in the damaged area trigger pain and other sensory impulses. Simultaneously, the smooth muscles in the vessel wall contract, resulting in a vascular spasm. This contraction reduces the vessel's diameter at the injury site, slowing or stopping blood loss through the vessel wall. Vascular spasms typically last for...

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Related Experiment Video

Updated: May 29, 2026

A Liposome Membrane Permeability Assay for Investigating the Effects of Phosphatidylinositol Phosphate Groups on Membranotropic Action of Venom PLA2
10:31

A Liposome Membrane Permeability Assay for Investigating the Effects of Phosphatidylinositol Phosphate Groups on Membranotropic Action of Venom PLA2

Published on: September 26, 2025

Phospholipase A(2) activates hemostasis.

Thomas W Stief1

  • 1Department of Clinical Chemistry, University Hospital Giessen & Marburg, Germany.

Drug Target Insights
|September 9, 2011
PubMed
Summary

Phospholipases A(2) (PLA(2)) enzymes activate blood coagulation, leading to pathological disseminated intravascular coagulation (PDIC). Early diagnosis by screening patients for plasmatic thrombin activity is crucial for life-threatening conditions.

Keywords:
PDICPLA2Phospholipasecontact phaseintrinsic hemostasisthrombin

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The Nijmegen Hemostasis Assay: Simultaneous Fluorogenic Measurement of Thrombin and Plasmin Generation in a Single Well
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Last Updated: May 29, 2026

A Liposome Membrane Permeability Assay for Investigating the Effects of Phosphatidylinositol Phosphate Groups on Membranotropic Action of Venom PLA2
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The Nijmegen Hemostasis Assay: Simultaneous Fluorogenic Measurement of Thrombin and Plasmin Generation in a Single Well
08:01

The Nijmegen Hemostasis Assay: Simultaneous Fluorogenic Measurement of Thrombin and Plasmin Generation in a Single Well

Published on: February 27, 2026

Area of Science:

  • Biochemistry
  • Hematology
  • Enzymology

Background:

  • Phospholipases A(2) (PLA(2)) are enzymes that degrade cell membrane phospholipids.
  • PLA(2) activity can initiate the kallikrein-mediated contact phase of coagulation.
  • Elevated PLA(2) levels are observed in conditions like trauma, pancreatitis, and sepsis.

Purpose of the Study:

  • To investigate the effect of PLA(2) on thrombin generation in human blood.
  • To quantify thrombin generation in recalcified plasma after exposure to PLA(2).

Main Methods:

  • Citrated whole blood was incubated with bovine pancreatic or snake PLA(2), LPS, or zymosan A.
  • Plasma was recalcified and thrombin generation was measured using a chromogenic assay.
  • Arginine was used to stop the coagulation reaction and depolymerize fibrin.

Main Results:

  • PLA(2) induced dose-dependent thrombin generation, comparable to LPS and zymosan A.
  • Thrombin generation was proportional to PLA(2) concentration up to 60 ng/ml.
  • High PLA(2) concentrations (10 μg/ml) also induced significant thrombin generation, unlike in control plasma.

Conclusions:

  • Elevated plasmatic PLA(2) activates the hemostasis system, potentially causing pathological disseminated intravascular coagulation (PDIC).
  • Screening for plasmatic thrombin activity is recommended for early diagnosis of these critical conditions.