ReviewCurrent research in toxicology2026
Polylactic acid microplastics as metabolic disruptors: Linking gut dysbiosis to systemic toxicity by disrupting microbiota-host co-metabolism.
Review in Current research in toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Pathogenesis of Micro/Nanoplastics in Mammalian Systems: Gut to Systemic Multi-Organ Dysfunction.Research (Washington, D.C.) · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The increasing application of polylactic acid (PLA) in consumer products leads to the widespread environmental distribution of its micro- and nano-plastics (PLA-MNPs). These particles pose potential health risks following environmental exposure, yet the mechanisms underlying their systemic toxicity remain inadequately defined. This review synthesizes current evidence demonstrating that PLA-MNPs accumulate in the intestine, compromising the gut barrier and inducing dysbiosis of the gut microbiota. We also explore the hypothetical role of disrupted gut microbiota-host co-metabolism - particularly involving aromatic amino acid pathways such as tryptophan metabolism - as a potential mechanism linking PLA-MNPs exposure to intestinal inflammation and injury, while acknowledging the current lack of direct experimental evidence for PLA-MNPs-specific effects on these pathways. By integrating literature on the gut-liver axis, we further elucidate how intestinal injury propagates to systemic metabolic disturbances. This overview aims to provide a structured synthesis of existing findings, identify key knowledge gaps, and suggest targeted approaches for future mechanistic and exposure-informed risk assessment of PLA-MNPs.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.