dc.contributor.author
Schreck, Katharina
dc.contributor.author
Melzig, Matthias F.
dc.date.accessioned
2018-10-29T09:16:22Z
dc.date.available
2018-10-29T09:16:22Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/23125
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-919
dc.description.abstract
The intestinal absorption of fatty acids, glucose and fructose is part of the basic requirements for the provision of energy in the body. High access of saturated long-chain fatty acids (LCFA), glucose and fructose can facilitate the development of metabolic diseases, particularly the metabolic syndrome and type-2 diabetes mellitus (T2DM). Research has been done to find substances which decelerate or inhibit intestinal resorption of these specific food components. Promising targets are the inhibition of intestinal long-chain fatty acid (FATP2, FATP4), glucose (SGLT1, GLUT2) and fructose (GLUT2, GLUT5) transporters by plant extracts and by pure substances. The largest part of active components in plant extracts belongs to the group of polyphenols. This review summarizes the knowledge about binding sites of named transporters and lists the plant extracts which were tested in Caco-2 cells regarding uptake inhibition.
en
dc.format.extent
29 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Caco-2 cells
en
dc.subject
plant extracts
en
dc.subject
uptake inhibition
en
dc.subject
intestinal transporters
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik
dc.title
Intestinal Saturated Long-Chain Fatty Acid, Glucose and Fructose Transporters and Their Inhibition by Natural Plant Extracts in Caco-2 Cells
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.3390/molecules23102544
dcterms.bibliographicCitation.journaltitle
Molecules
dcterms.bibliographicCitation.number
10
dcterms.bibliographicCitation.volume
23
dcterms.bibliographicCitation.url
https://doi.org/10.3390/molecules23102544
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Pharmazie
refubium.funding
Institutional Participation
refubium.funding.id
MDPI
refubium.note.author
Die Publikation wurde aus Open Access Publikationsgeldern der Freien Universität Berlin und der DFG gefördert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dc.relation.hascorrection
https://refubium.fu-berlin.de/handle/fub188/23650
dcterms.isPartOf.issn
1420-3049