Microplastic-Induced Disruption of Intestinal Barrier Integrity and Triggering Neuroinflammatory Responses Through

Arya Ghosh1, Varnita Karmakar1, Baishakhi Saha2

  • 1Department of Pharmaceutical Sciences and Technology, Birla Institute of Technology, Mesra, Ranchi, 835215, Jharkhand, India.

Insights

Microplastics (MPs) harm gut health and brain function by disrupting the gut-brain axis (GBA). Polyethylene and polypropylene MPs cause intestinal damage, inflammation, and neurotoxicity, with polyethylene showing greater effects.

Area of Science:

  • Environmental toxicology
  • Neuroscience
  • Gastroenterology

Background:

  • Microplastics (MPs) are pervasive environmental contaminants.
  • Their impact on the gut-brain axis (GBA) and associated neurotoxicity is not fully understood.
  • Polyethylene (PE) and polypropylene (PP) are common MP types.

Purpose of the Study:

  • To investigate the effects of PE and PP MPs on intestinal barrier integrity, oxidative stress, neuroinflammation, and synaptic dysfunction.
  • To elucidate the role of MPs in gut-brain axis dysregulation.
  • To compare the toxicity of PE-MPs and PP-MPs.

Main Methods:

  • Physicochemical characterization of MPs.
  • Oral administration of PE- and PP-MPs (10 and 100 mg/kg BW) to experimental animals for 45 days.
  • Assessment of intestinal barrier integrity, gut microbiota, oxidative stress, neuroinflammation, neurochemical markers, and behavioral changes.

Main Results:

  • MP exposure disrupted intestinal barrier integrity and altered short-chain fatty acid profiles.
  • Evidence of oxidative stress, inflammation in the gut and brain, and altered neurochemical markers.
  • Behavioral abnormalities, increased amyloid precursor protein (APP), and tau pathology indicated GBA impairment.
  • PE-MPs exhibited greater toxicity than PP-MPs, especially at higher doses.

Conclusions:

  • Chronic exposure to PE and PP MPs disrupts intestinal homeostasis.
  • MPs promote neuroinflammatory toxicity via gut-brain axis dysregulation.
  • PE MPs appear more toxic than PP MPs at equivalent doses.

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