Acetaminophen changes intestinal epithelial cell membrane properties, subsequently affecting absorption processes.
نویسندگان
چکیده
BACKGROUND/AIMS Acetaminophen (APAP) effects on intestinal barrier properties are less investigated. APAP may lead to a changed bioavailability of a subsequently administered drug or diet in the body. We investigated the influence of APAP on enterocytic cell membrane properties that are able to modify the net intestinal absorption of administered substances across the Caco-2 barrier model. METHODS The effect of APAP on cytotoxicity was measured by LDH assay, TER value and cell capacitance label-free using impedance monitoring, membrane permeability by FITC-dextrans, and efflux transporter MDR1 activity by Rh123. APAP levels were determined by HPLC analysis. Cell membrane topography and microvilli were investigated using SEM and intestinal alkaline phosphatase (Alpi) and tight junction protein 1 (TJP1) expression by western blot analysis. RESULTS APAP changed the apical cell surface, reduced the number of microvilli and protein expression of Alpi as a brush border marker and TJP1, increased the membrane integrity and concurrently decreased cell capacitance over time. In addition, APAP decreased the permeability to small molecules and increased the efflux transporter activity, MDR1. CONCLUSION APAP alters the Caco-2 cell membrane properties by different mechanisms and reduces the permeability to administered substances. These findings may help to optimize therapeutic implications.
منابع مشابه
Biol. Pharm. Bull. 30(10) 1982—1986 (2007)
cently been identified as important factors affecting drug disposition. The effects of these factors on drug absorption are thought to vary depending on the epithelial barrier functions and transporters. Ingestion of many types of herbal supplements results in interactions with drugs administered concomitantly. The intestinal mucosal epithelium constitutes the major barrier (including tight jun...
متن کاملCircadian modulation in the intestinal absorption of P-glycoprotein substrates in monkeys.
Recent studies in laboratory rodents have revealed that circadian oscillation in the physiologic functions affecting drug disposition underlies the dosing time-dependent change in pharmacokinetics. However, it is difficult to predict the circadian change in the drug pharmacokinetics in a diurnal human by using the data collected from nocturnal rodents. In this study, we used cynomolgus monkeys,...
متن کاملThe Gastrointestinal Tract and Iron Absorption.
IT HAS BEEN demonstrated repeatedly that intestinal absorption of iron is responsive to the body’s needs; enhanced absorption being found with increased need,’-5 and diminished absorption with decreased need.”5’6 Thus there is agreement that intestinal iron absorption is regulated, but there is no general agreement as to the nature of the regulatory mechanism. As part of all previous hypotheses...
متن کاملSoluble uric acid induces inflammation via TLR4/NLRP3 pathway in intestinal epithelial cells
Objective(s): Hyperuricemia is a risk for cardiovascular and metabolic diseases, but the mechanism is ambiguous. Increased intestinal permeability is correlated with metabolic syndrome risk factors. Intestinal epithelial cells play a pivotal role in maintaining intestinal permeability. Uric acid is directly eliminated into intestinal lumen, however, the mechanism and e...
متن کاملMol096735 29..37
Recent studies in laboratory rodents have revealed that circadian oscillation in the physiologic functions affecting drug disposition underlies the dosing time-dependent change in pharmacokinetics. However, it is difficult to predict the circadian change in the drug pharmacokinetics in a diurnal human by using the data collected from nocturnal rodents. In this study, we used cynomolgus monkeys,...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
دوره 32 2 شماره
صفحات -
تاریخ انتشار 2013