Abstract

Matrix-assisted laser desorption/ionisation mass spectrometry imaging (MALDI-MSI) is presently used in physiological evaluations for visualisation of targets in organs. In the present study, MALDI-MSI was used as a visualisation technique to investigate the intestinal absorption of polyphenols. Nifedipine/phytic acid-aided MALDI-MSI was performed to visualise theaflavin-3′-O-gallate (TF3′G) and epicatechin-3-O-gallate (ECG) in the rat jejunum for 50-µM, 60-min transport experiments. Non-absorbable TF3′G was successfully visualised at the apical region, whereas absorbable ECG was detected throughout the rat jejunum. MALDI-MSI was also performed to determine the transport routes of the target metabolites. Signals corresponding to TF3′G and ECG in the membranes were diminished following treatment with inhibitors targeting the monocarboxylic acid transporter and organic anion transporting polypeptides. Enhanced visualisation of TF3′G was achieved by inhibiting efflux routes. Our findings demonstrated that the present MALDI-MSI can provide critical spatial informations on intestinal absorption of targets, by which TF3′G and ECG were incorporated into intestinal tissues, followed by efflux back to the apical compartment. In addition, MALDI-MSI analyses suggested that TF3′G was resistant to phase II metabolism during the influx/efflux processes, whereas ECG was susceptible to methylation and sulphation reactions. In conclusion, inhibitor-aided MALDI-MSI could serve as a powerful in situ visualisation technique for verifying intestinal transport routes and investigating the metabolism of penetrants.

Highlights

  • Matrix-assisted laser desorption/ionsation mass spectrometry imaging (MALDI-MSI) is a promising in situ analytical tool that can be used in pharmacological studies

  • The present study highlighted the potential use of MALDI-MSI as a novel approach for pharmacological studies; in turn, MALDI-MSI has advantage as non-targeting analysis based on m/z, providing direct evidence on the location of interesting analytes in tissues without chromatographic separation by LC-MS

  • The nifedipine/ phytic acid-aided MALDI-MSI technique is an in situ visualisation technique that successfully and clearly verified the location, transport route(s), and metabolism of the target polyphenols, namely, absorbable ECG and non-absorbable TF3′G, in the SD rat jejunum

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Summary

Introduction

Matrix-assisted laser desorption/ionsation mass spectrometry imaging (MALDI-MSI) is a promising in situ analytical tool that can be used in pharmacological studies. In our previous absorption study on theaflavins (TFs) in 60-min-Caco-2 cell transport, TFs were not detected on the basolateral side by liquid chromatography-time-of-flight-mass spectrometry (LC-TOF-MS)[18] Regardless of their non-absorption properties, TFs were found to play physiological roles in the regulation of intestinal transport routes. TF3′G was suggested to suppress the expression of intestinal peptide transporter 1 (PepT1) and upregulate the expression of the tight junction (TJ) proteins in Caco-2 cells via the activation of AMP-activated protein kinase (AMPK)[18,19] These findings led to a speculation that TFs must exert physiological function in the intestinal tissue, it remains unclear whether TFs could enter the intracellular side of the intestinal membrane. Our previous studies showed that nifedipine enhanced the ionisation of less-ionisable polyphenols (e.g., flavonols, flavones, flavanones, flavonones, chalcones, stilbenoids, and phenolic acids), by removal of a proton from the polyphenol skeleton due to its photobase properties[20]

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