Related Experiment Video
Updated: Feb 2, 2026

Continuous Noninvasive Measuring of Crayfish Cardiac and Behavioral Activities
Published on: February 6, 2019
Using the magnetoencephalogram to noninvasively measure magnetite in the living human brain
Sheraz Khan1,2, David Cohen1,2,3
1Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Abstract:
During the past several decades there has been much interest in the existence of magnetite particles in the human brain and their accumulation with age. These particles also appear to play an important role in neurodegenerative diseases of the brain. However, up to now the amount and distribution of these particles has been measured only in post-mortem brain tissue. Although in-vivo MRI measurements do show iron compounds generally, MRI cannot separate them according to their magnetic phases, which are associated with their chemical interactions. In contrast, we here offer a new noninvasive, in-vivo method which is selectively sensitive only to particles which can be strongly magnetized. We magnetize these particles with a strong magnetic field through the head, and then measure the resulting magnetic fields, using the dcMagnetoencephalogram (dcMEG). From these data, the mass and locations of the particles can be estimated, using a distributed inverse solution. To test the method, we measured 11 healthy male subjects (ages 19-89 year). Accumulation of magnetite, in the hippocampal formation or nearby structures, was observed in the older men. These in-vivo findings agree with reports of post-mortem measurements of their locations, and of their accumulation with age. Thus, our findings allow in-vivo measurement of magnetite in the human brain, and possibly open the door for new studies of neurodegenerative diseases of the brain.
Related Concept Videos
Mechanical Ventilation III: Noninvasive Ventilation
Noninvasive Positive-Pressure Ventilation...
Measurement: Standard Units
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Biodiversity and Human Values
Measures of Central Tendency
Measuring Reaction Rates

