From Furniture To Shampoo
By CASE WESTERN RESERVE UNIVERSITY
New research indicates that chemicals found in countless household products can damage specialized brain cells.
A team of researchers from the Case Western Reserve
University School of Medicine has provided fresh insight into the dangers some
common household chemicals pose to brain health. They suggest that chemicals
found in a wide range of items, from furniture to hair products, may be linked
to neurological diseases like multiple sclerosis and autism spectrum disorders.
Neurological problems impact millions of people, but only
a fraction of cases can be attributed to genetics alone, indicating that
unknown environmental factors are important contributors to neurological
disease.
The new study published in the journal Nature Neuroscience, discovered that some common home chemicals specifically affect the brain’s oligodendrocytes, a specialized cell type that generates the protective insulation around nerve cells.
“Loss of oligodendrocytes underlies multiple sclerosis
and other neurological diseases,” said the study’s principal investigator, Paul
Tesar, the Dr. Donald and Ruth Weber Goodman Professor of Innovative
Therapeutics and director of the Institute for Glial Sciences at the School of
Medicine. “We now show that specific chemicals in consumer products can
directly harm oligodendrocytes, representing a previously unrecognized risk
factor for neurological disease.”
Chemicals of Concern and Their Effects
On the premise that not enough thorough research has been
done on the impact of chemicals on brain health, the researchers analyzed over
1,800 chemicals that may be exposed to humans. They identified chemicals that
selectively damaged oligodendrocytes belong to two classes: organophosphate
flame retardants and quaternary ammonium compounds.
Since quaternary ammonium compounds are present in many
personal-care products and disinfectants, which are being used more frequently
since the COVID-19 pandemic began, humans are regularly exposed
to these chemicals. And many electronics and furniture include organophosphate
flame retardants.
The researchers used cellular and organoid systems in the
laboratory to show that quaternary ammonium compounds cause oligodendrocytes to
die, while organophosphate flame retardants prevented the maturation of
oligodendrocytes.
Implications for Human Health
They demonstrated how the same chemicals damage
oligodendrocytes in the developing brains of mice. The researchers also linked
exposure to one of the chemicals to poor neurological outcomes in children
nationally.
“We found that oligodendrocytes—but not other brain
cells—are surprisingly vulnerable to quaternary ammonium compounds and
organophosphate flame retardants,” said Erin Cohn, lead author and graduate
student in the School of Medicine’s Medical Scientist Training Program.
“Understanding human exposure to these chemicals may help explain a missing
link in how some neurological diseases arise.”
The association between human exposure to these chemicals
and effects on brain health requires further investigation, the experts warned.
Future research must track the chemical levels in the brains of adults and
children to determine the amount and length of exposure needed to cause or
worsen disease.
“Our findings suggest that more comprehensive scrutiny of
the impacts of these common household chemicals on brain health is necessary,”
Tesar said. “We hope our work will contribute to informed decisions regarding
regulatory measures or behavioral interventions to minimize chemical exposure
and protect human health.”
Reference: “Pervasive environmental chemicals impair
oligodendrocyte development” by Erin F. Cohn, Benjamin L. L. Clayton, Mayur
Madhavan, Kristin A. Lee, Sara Yacoub, Yuriy Fedorov, Marissa A. Scavuzzo,
Katie Paul Friedman, Timothy J. Shafer and Paul J. Tesar, 25 March 2024, Nature Neuroscience.
DOI: 10.1038/s41593-024-01599-2
Additional contributing researchers from Case Western
Reserve School of Medicine and from the U.S. Environmental Protection Agency
included Benjamin Clayton, Mayur Madhavan, Kristin Lee, Sara Yacoub, Yuriy
Fedorov, Marissa Scavuzzo, Katie Paul Friedman, and Timothy Shafer.
The research was supported by grants from the National Institutes of Health, National Multiple Sclerosis
Society, Howard Hughes Medical Institute, and New York Stem Cell Foundation,
and philanthropic support by sTF5 Care and the Long, Walter, Peterson, Goodman
and Geller families.