Endpoint | Key finding |
---|---|
Clinical pathology | High dose oral application of SiO2 and Ag nanoparticles had no detectable effects on established clinical pathology endpoints in male Wistar rats |
Gut microbiome | Ingested SiO2 and Ag nanoparticles altered the gut microbiome significantly |
 | SiO2 and Ag NP influence the level of microbial genera some of which are known to mediate probiotic or adverse effects |
 | The gut microbiome is a sensitive indicator for possible hazards caused by orally administrated NP |
Plasma metabolome | Orally applied SiO2 and Ag NP led to changes in the level of several plasma metabolites known to be crucial for human health |
 | Key plasma metabolites (e.g. gut-microbiota derived IAA) are suitable markers for potential adverse effects induced by orally applied NP |
Combined gut microbiome and plasma metabolome | The combination of gut microbiome and plasma metabolome profiling has a strong potential as a sensitive tool to disclose early detrimental effects of ingested NP |