Intestine-Liver-on-chip systems can be useful to predict oral drug administration and first-pass metabolism in order to partly replace the animal model. While organ-on-chip technology can count on sophisticated micro-physiological devices, the engineered organs still remain artificial surrogates of the native counterparts. Here, we used a bottom-up tissue engineering strategy to build-up physiologically functional 3D Human Intestine Model (3D-HIM) as well as 3D Liver-microtissues (HepG2-μTPs) and designed a microfluidic Intestine-Liver-On-Chip (InLiver-OC) to emulate first-pass mechanism occurring . Our results highlight the ethanol-induced 3D-HIM hyper-permeability and stromal injury, the intestinal prevention on the liver injury, as well as the synergic contribution of the two 3D tissue models on the release of metabolic enzymes after high amount of ethanol administration.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090126PMC
http://dx.doi.org/10.3389/fbioe.2020.00163DOI Listing

Publication Analysis

Top Keywords

first-pass metabolism
8
intestine-liver axis
4
axis on-chip
4
on-chip reveals
4
reveals intestinal
4
intestinal protective
4
protective role
4
role hepatic
4
hepatic damage
4
damage emulating
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!