Literature DB >> 7738690

A Na(+)-dependent mechanism is involved in mucosal uptake of cinnamic acid across the jejunal brush border in rats.

S Wolffram1, T Weber, B Grenacher, E Scharrer.   

Abstract

Phenolic acids are present in all plant-derived foods and in most diets. Indirect evidence indicates substantial absorption of phenolic monomers from the gastrointestinal tract. However, the mechanisms involved in the absorptive process are unknown. The present study investigates mucosal uptake of radioactively labeled cinnamic acid as a model substance for monomeric cinnamic acid derivatives (e.g., cinnamic, ferulic or caffeic acid) in the rat jejunum using an in vitro mucosal uptake technique. The results indicate the existence of a Na(+)-dependent saturable transport mechanism for uptake of cinnamic acid across the jejunal brush border membrane. The observed Na+ dependence of jejunal cinnamate uptake seems not to be related to the activity of the Na+,H+ exchanger. Lowering the pH of the incubation medium resulted in a pronounced increase in mucosal cinnamate uptake that can be only partially explained by an increase in nonionic diffusion of cinnamic acid. Furthermore, jejunal uptake of cinnamate seems to be influenced by intracellular HCO3- and/or pH, since the addition of methazolamide to a HCO3(-)- and CO2-free incubation medium significantly inhibited mucosal cinnamate uptake, whereas methazolamide was without an effect in the presence of HCO3- and CO2 in the incubation medium. Unlabeled cinnamic and ferulic acid as well as short-chain fatty acids (acetic, propionic and butyric acid) significantly inhibited Na(+)-dependent uptake of radioactivity labeled cinnamic acid.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7738690     DOI: 10.1093/jn/125.5.1300

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  6 in total

1.  The bioavailability of polyphenols is highly governed by the capacity of the intestine and of the liver to secrete conjugated metabolites.

Authors:  M Silberberg; C Morand; T Mathevon; C Besson; C Manach; A Scalbert; C Remesy
Journal:  Eur J Nutr       Date:  2005-06-30       Impact factor: 5.614

2.  Differential distribution of ferulic acid to the major plasma constituents in relation to its potential as an antioxidant.

Authors:  C Castelluccio; G P Bolwell; C Gerrish; C Rice-Evans
Journal:  Biochem J       Date:  1996-06-01       Impact factor: 3.857

3.  Butyric acid increases transepithelial transport of ferulic acid through upregulation of the monocarboxylate transporters SLC16A1 (MCT1) and SLC16A3 (MCT4).

Authors:  Kerstin Ziegler; Asimina Kerimi; Laure Poquet; Gary Williamson
Journal:  Arch Biochem Biophys       Date:  2016-02-09       Impact factor: 4.013

Review 4.  Cinnamic Acid and Its Derivatives: Mechanisms for Prevention and Management of Diabetes and Its Complications.

Authors:  Sirichai Adisakwattana
Journal:  Nutrients       Date:  2017-02-21       Impact factor: 5.717

Review 5.  Ferulic Acid From Plant Biomass: A Phytochemical With Promising Antiviral Properties.

Authors:  Io Antonopoulou; Eleftheria Sapountzaki; Ulrika Rova; Paul Christakopoulos
Journal:  Front Nutr       Date:  2022-02-07

Review 6.  Hydroxycinnamic acid derivatives: a potential class of natural compounds for the management of lipid metabolism and obesity.

Authors:  Md Ashraful Alam; Nusrat Subhan; Hemayet Hossain; Murad Hossain; Hasan Mahmud Reza; Md Mahbubur Rahman; M Obayed Ullah
Journal:  Nutr Metab (Lond)       Date:  2016-04-11       Impact factor: 4.169

  6 in total

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