2007
DOI: 10.1016/j.cbi.2007.06.006
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Modulating hesperetin bioavailability at the level of its intestinal metabolism and ABC transporter mediated efflux studied in Caco-2 monolayers

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Cited by 3 publications
(3 citation statements)
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“…It is now clear that many flavonoid conjugates interact with ABC transporters, and that these transporters are crucial for determining their distribution around the body. For example, ABCC2 is situated on the brush border of small intestine enterocytes, and effluxes some conjugates back towards the gut lumen and, in effect, these compounds per se are no longer bioavailable to the body (Brand, van der Wel, Williamson, van Bladeren, & Rietjens, ; Williamson et al., ). ABCG2 also plays an important role in the efflux of flavonoid conjugates from cells (Zhang, Yang, & Morris, ).…”
Section: Interaction Of Flavonoids With the Gastrointestinal Tractmentioning
confidence: 99%
“…It is now clear that many flavonoid conjugates interact with ABC transporters, and that these transporters are crucial for determining their distribution around the body. For example, ABCC2 is situated on the brush border of small intestine enterocytes, and effluxes some conjugates back towards the gut lumen and, in effect, these compounds per se are no longer bioavailable to the body (Brand, van der Wel, Williamson, van Bladeren, & Rietjens, ; Williamson et al., ). ABCG2 also plays an important role in the efflux of flavonoid conjugates from cells (Zhang, Yang, & Morris, ).…”
Section: Interaction Of Flavonoids With the Gastrointestinal Tractmentioning
confidence: 99%
“…52 Many flavonoid adducts have been well studied for their interactions with ATP-binding cassette transporter proteins, which are critical in determining their distribution in vivo. 53 Metabolism and transport back to the lumen from the enterocyte via the ATP-binding cassette transporter is thought to limit the bioavailability of flavonoids.…”
Section: Bioavailability Of Flavonoid Compoundsmentioning
confidence: 99%
“…It has been shown that genistein can interact with the family of transporter proteins (OATP1B1), and further studies have shown that the flavonoids mangiferin and silymarin interact with human OAT1, whereas quercetin, naringenin, and naringenin‐7‐ O ‐rutinoside (Narirutin) do not 52 . Many flavonoid adducts have been well studied for their interactions with ATP‐binding cassette transporter proteins, which are critical in determining their distribution in vivo 53 . Metabolism and transport back to the lumen from the enterocyte via the ATP‐binding cassette transporter is thought to limit the bioavailability of flavonoids.…”
Section: Bioavailability Of Flavonoid Compoundsmentioning
confidence: 99%