Literature DB >> 2000635

Gastrointestinal absorption of paraquat in the isolated mucosa of the rat.

J R Heylings1.   

Abstract

The gastrointestinal absorption of paraquat (1,1'-dimethyl-4,4'-bipyridylium) was studied using the isolated mucosa from different regions of the gastrointestinal tract of rats. Tissues were stripped of their muscle layers and the viability of the mucosa was maintained in flux chambers by bathing both serosal and luminal membranes with separate oxygenated solutions. Paraquat absorption, transmucosal potential difference (PD), and permeability of the mucosa were studied. Exposure of the luminal side of isolated mucosae to paraquat (100 mg/ml) resulted in greater paraquat absorption across the small intestine compared to other regions of the gastrointestinal tract. The descending order of tissue absorption (as %/cm2 mucosa) was jejunum (17.6 +/- 0.8%), ileum (10 +/- 2.7%), colon (5.7 +/- 3.2%), duodenum (5.5 +/- 1.3%), stomach (2 +/- 0.8%), and esophagus (0.5 +/- 0.7%). Mucosal uptake of paraquat in the ileum was nonlinear over a luminal concentration range 2-200 mg/ml. Three phases to paraquat absorption were identified in this region of the small intestine: (i) a rate which was faster than diffusion (2-20 mg/ml paraquat); (ii) a rate which was slower than diffusion and obeyed saturation kinetics, with an apparent Km = 116 mM and Vmax = 11.3 mumol/g/hr, at paraquat concentrations up to 150 mg/ml: and (iii) a rate similar to that of diffusion at 200 mg/ml paraquat. Paraquat absorption at 200 mg/ml was also associated with an increase in mucosal permeability and reduction in PD. Inhibition of tissue metabolism resulted in a linear or diffusional paraquat absorption over a wide luminal concentration range (2-200 mg/ml). It is suggested, therefore, that paraquat absorption in the rat occurs principally in the small intestine and by a mechanism which consists of facilitated, saturable, and diffusional components. Knowledge of the mechanism by which paraquat gains entry to the bloodstream may offer new approaches to the development of safer formulations of the herbicide.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 2000635     DOI: 10.1016/0041-008x(91)90311-2

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  4 in total

1.  Acute and chronic stress-induced oxidative gastrointestinal mucosal injury in rats and protection by bismuth subsalicylate.

Authors:  D Bagchi; O R Carryl; M X Tran; M Bagchi; A Garg; M M Milnes; C B Williams; J Balmoori; D J Bagchi; S Mitra; S J Stohs
Journal:  Mol Cell Biochem       Date:  1999-06       Impact factor: 3.396

2.  Protection against chemically-induced oxidative gastrointestinal tissue injury in rats by bismuth salts.

Authors:  D Bagchi; O R Carryl; M X Tran; M Bagchi; P J Vuchetich; R L Krohn; S D Ray; S Mitra; S J Stohs
Journal:  Dig Dis Sci       Date:  1997-09       Impact factor: 3.199

3.  Transport characteristics of paraquat across rat intestinal brush-border membrane.

Authors:  M Nagao; H Saitoh; W D Zhang; K Iseki; Y Yamada; T Takatori; K Miyazaki
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

4.  Improvement in survival after paraquat ingestion following introduction of a new formulation in Sri Lanka.

Authors:  Martin F Wilks; Ravindra Fernando; P L Ariyananda; Michael Eddleston; David J Berry; John A Tomenson; Nicholas A Buckley; Shaluka Jayamanne; David Gunnell; Andrew Dawson
Journal:  PLoS Med       Date:  2008-02       Impact factor: 11.069

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.