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Pulmonary Flora‐Derived Lipopolysaccharide Mediates Lung‐Brain Axis through Activating Microglia Involved in Polystyrene Microplastic‐Induced Cognitive Dysfunction
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In a mouse study, inhaling polystyrene microplastics impaired learning and memory -- even though the plastics never reached the brain directly. Instead, the microplastics changed the bacterial community in the lungs, which produced inflammatory signals that traveled to the brain and triggered damage, revealing a lung-to-brain pathway for microplastic harm.
Microplastics (MPs) have been detected in the atmospheric and the human respiratory system, indicating that the respiratory tract is a significant exposure route for MPs. However, the effect of inhaled MPs on cognitive function has not been adequately studied. Here, a C57BL/6 J mouse model of inhalation exposure to polystyrene MPs (PS-MPs, 5 µm, 60 d) is established by intratracheal instillation. Interestingly, in vivo fluorescence imaging and transmission electron microscopy reveal that PS-MPs do not accumulate in the brain. However, behavioral experiments shows that cognitive function of mice is impaired, accompanied by histopathological damage of lung and brain tissue. Transcriptomic studies in hippocampal and lung tissue have demonstrated key neuroplasticity factors as well as cognitive deficits linked to lung injury, respectively. Mechanistically, the lung-brain axis plays a central role in PS-MPs-induced neurological damage, as demonstrated by pulmonary flora transplantation, lipopolysaccharide (LPS) intervention, and cell co-culture experiments. Together, inhalation of PS-MPs reduces cognitive function by altering the composition of pulmonary flora to produce more LPS and promoting M1 polarization of microglia, which provides new insights into the mechanism of nerve damage caused by inhaled MPs and also sheds new light on the prevention of neurotoxicity of environmental pollutants.
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Mice that consumed polystyrene microplastics over an extended period showed reduced immune cells called macrophages in their colons and changes in gut bacteria that were linked to altered brain chemistry. This study provides evidence for a gut-brain connection where microplastics may affect brain function indirectly by first disrupting gut health and the immune system.
Exposure to polystyrene microplastics impairs hippocampus-dependent learning and memory in mice
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Researchers found that mice exposed to polystyrene microplastics for eight weeks showed impaired learning and memory, with plastic particles detected in their hippocampus, the brain region critical for memory formation. The microplastics caused neuroinflammation, disrupted synaptic signaling, and altered gene expression in the brain. Interestingly, cutting the vagus nerve partially prevented these effects, suggesting that gut-brain communication plays a role in how ingested microplastics affect cognitive function.
Oral exposure of polystyrene microplastics and doxycycline affects mice neurological function via gut microbiota disruption: The orchestrating role of fecal microbiota transplantation
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Mice exposed to both polystyrene microplastics and the antibiotic doxycycline showed brain inflammation and declines in learning and memory, driven by disruptions to their gut bacteria. Fecal transplants from healthy mice reversed some of these brain effects, confirming the gut-brain connection plays a key role. This suggests that microplastics combined with common antibiotics could harm brain function through changes in the gut microbiome.
Polystyrene Microplastics Disrupt the Gut-Brain Axis via Activating Brain TLR4 and Impair Hippocampal Synapses through the TLR4/MyD88/NF-κB Pathway
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Scientists found that tiny plastic particles from polystyrene (commonly used in food containers and packaging) can damage the connection between your gut and brain when consumed. These microplastics disrupt healthy gut bacteria, allowing harmful substances to enter the bloodstream and eventually reach the brain, where they cause inflammation and damage to areas important for memory and learning. This research suggests that exposure to these tiny plastic particles could potentially contribute to brain health problems over time.
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Researchers found that inhaled polystyrene nanoplastics worsen asthma in mice by triggering a chain reaction involving gut bacteria disruption, nerve-immune signaling, and airway inflammation, revealing a gut-lung connection where plastic particles in the body can amplify respiratory disease through multiple biological pathways at once.
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