کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5860875 1562637 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
In vitro study of intestinal transport of arsenite, monomethylarsonous acid, and dimethylarsinous acid by Caco-2 cell line
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
In vitro study of intestinal transport of arsenite, monomethylarsonous acid, and dimethylarsinous acid by Caco-2 cell line
چکیده انگلیسی

Arsenic is a pollutant widely distributed in the environment. There are numerous studies on the toxicity of trivalent arsenic forms As(III), MMA(III), and DMA(III), but few data are available on the processes of digestion and absorption of these arsenic species and the mechanisms involved are unknown. The present study evaluated the processes involved in intestinal absorption of trivalent arsenic species, using the Caco-2 cell model as system. The apparent permeability values obtained for As(III) in apical-basolateral direction (4.6 ± 0.3) × 10−6 cm/s, showing moderate intestinal absorption. Transport of MMA(III) [Papp = (7.0 ± 0.9) × 10−6 cm/s] and DMA(III) [Papp = (10.6 ± 1.4) × 10−6 cm/s] is greater than that of As(III). The cellular retention of As(III) (0.9-2.4%) was less than that observed for MMA(III) (30%) and DMA(III) (35%).A substantial paracellular component was observed in transport of As(III) and MMA(III), whereas DMA(III) does not use this pathway for its absorption. For all the trivalent species, transport depends on temperature, with an active transcellular component for MMA(III) and DMA(III). Variations in pH do not affect transport of these species. The presence of GSH and green tea extract significantly alters transport of As(III) across Caco-2 cells.

► Paracellular transport of As(III) and MMA(III) in Caco-2 cell line. ► Active transcellular component for MMA(III) and DMA(III) transport in Caco-2 cell line. ► pH does not affect transport of As(III), MMA(III) and DMA(III) in Caco-2 cell line.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology Letters - Volume 204, Issues 2–3, 28 July 2011, Pages 127-133
نویسندگان
, , , ,