Jpe. Spencer et al., Epicatechin is the primary bioavailable form of the procyanidin dimers B2 and B5 after transfer across the small intestine, BIOC BIOP R, 285(3), 2001, pp. 588-593
Citations number
30
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Perfusion of isolated small intestine with the procyanidin dimers B2 and 13
5 extracted from cocoa indicated that both forms of dimer are transferred t
o the serosal side of enterocytes but only to a very small extent (< 1% of
the total transferred flavanol-like compounds). However, perfusion of dimer
mainly resulted in large amounts of unmetabolised/unconjugated epicatechin
monomer being detected on the serosal side (95.8%). The cleavage of dimer
during transfer seemed to be energy-dependent, requiring an intact cell sys
tem, as incubation with jejunal homogenates failed to yield epicatechin. Lo
w levels methylated dimer were also detected (3.2%), but no conjugates and
metabolites of epicatechin indicating that metabolism of monomer and dimer
is limited during dimer cleavage/translocation. The methylation of dimer ma
y be by catechol-O-methyltransferase, however, at high concentrations of di
mer COMT activity is reduced leading to an inhibition of both monomer and d
imer O-methylation. (C) 2001 Academic Press.