Related Experiment Video
Updated: Feb 14, 2026

05:36
Standardized Model of Ventricular Fibrillation and Advanced Cardiac Life Support in Swine
Published on: January 30, 2020
8.5K
Electromechanical vortex filaments during cardiac fibrillation.
J Christoph1,2,3, M Chebbok2,4, C Richter1,2,4
1Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany.
Nature
|February 22, 2018
Summary
This study visualizes 3D mechanical scroll waves in the heart using ultrasound, revealing their role alongside electrical signals in cardiac fibrillation. These findings offer new avenues for diagnosing and treating heart arrhythmias.
Area of Science:
- Cardiology
- Biophysics
- Medical Imaging
Background:
- Scroll waves, or vortex-like rotating waves, drive complex patterns in excitable systems.
- Filament-like phase singularities from 3D scroll waves are key in cardiac arrhythmias.
- Understanding 3D dynamics of scroll waves in cardiac tissue is crucial but challenging.
Purpose of the Study:
- To visualize 3D spatiotemporal dynamics of mechanical scroll waves within the contracting heart wall.
- To investigate the coexistence and interaction of mechanical and electrical phase singularities during cardiac fibrillation.
- To characterize cardiac fibrillation using the dynamics of mechanical phase singularities.
Main Methods:
- Utilized high-resolution 4D ultrasound-based strain imaging to observe 3D mechanical scroll waves.
- Simultaneously measured membrane potential, intracellular calcium, and mechanical contractions.
- Analyzed trajectories, topological charge, and lifetime of electrical and mechanical phase singularities.
Main Results:
- Successfully visualized 3D mechanical scroll waves and filament-like phase singularities deep within the heart wall.
- Observed mechanical phase singularities coexisting with electrical phase singularities during cardiac fibrillation.
- Demonstrated complex interactions between electrical and mechanical phase singularities.
Conclusions:
- Cardiac fibrillation can be characterized by the 3D spatiotemporal dynamics of mechanical phase singularities originating in the ventricular wall.
- Electrical and mechanical phase singularities interact dynamically.
- Findings may lead to novel non-invasive diagnostic and therapeutic strategies for cardiac arrhythmias.
Related Concept Videos
Amyloid Fibrils
12.1K
Amyloid fibrils are aggregates of misfolded proteins. Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils.
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
12.1K
Amyloid Fibrils
6.5K
6.5K
Fibril-associated Collagen
3.4K
Fibril-associated collagens are a type of collagens present in the extracellular matrix with interrupted triple helices or FACIT (Fibril-associated collagens interrupted triple-helices). FACIT help connect and attach the collagen fibrils with each other as well as with other proteins of the extracellular matrix.
For example, the type II collagen fibrils in cartilage have covalently bound type IX fibril-associated collagens at regular intervals. Other types of fibril-associated collagens are...
For example, the type II collagen fibrils in cartilage have covalently bound type IX fibril-associated collagens at regular intervals. Other types of fibril-associated collagens are...
3.4K
Disassembly of Intermediate Filaments
2.7K
Intermediate filaments (IFs) do not undergo spontaneous disassembly. Enzymes, kinases, and phosphatases add and remove phosphates from specific sites to regulate their disassembly. The IF concentration in the cytoplasm also regulates the disassembly. If the concentration crosses a threshold, it activates the protein kinases in the vicinity, allowing the phosphorylation of IFs.
Keratin proteins, found at the cell periphery near cell junctions, undergo a cycle of assembly and disassembly. In Type...
Keratin proteins, found at the cell periphery near cell junctions, undergo a cycle of assembly and disassembly. In Type...
2.7K
Adaptability of Cytoskeletal Filaments
6.1K
The cytoskeleton is a complex dynamic structure performing varied functions based on cellular requirements. The adaptability of the individual filaments in the cytoskeleton determines their ability to perform various functions within the cell. It can undergo rapid reorganization during processes like cell division or remain stable for several hours as in the interphase. The adaptability of these filaments depends on stringent regulatory mechanisms. The microfilament and microtubules of the...
6.1K
Assembly of Cytoskeletal Filaments
28.0K
Cytoskeletal filaments are polymeric forms of smaller protein subunits. However, individual cytoskeletal filaments may easily disassemble or associate with other similar filaments to form rigid structures. Microfilaments, made of actin monomers, rely on actin-binding proteins to form bundles and create networks of individual actin filaments. Microtubules rely on microtubule-associated proteins (MAPs) to form sturdy cylindrical structures. However, the proteins involved in forming complex...
28.0K

