Bioavailability of Glucosyl Hesperidin in Rats

Mika Yamada(Hayashibara (Japan)), Fujimi Tanabe(Hayashibara (Japan)), Norie Arai(Hayashibara (Japan)), Hitoshi Mitsuzumi(Hayashibara (Japan)), Yoshikatsu Miwa(Hayashibara (Japan)), Michio Kubota(Hayashibara (Japan)), Hiroto Chaen(Hayashibara (Japan)), Masayoshi Kibata(Hayashibara (Japan))
Bioscience Biotechnology and Biochemistry
June 23, 2006
Cited by 143Open Access
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Abstract

Glucosyl hesperidin (G-hesperidin) is a water-soluble derivative of hesperidin. We compared the absorption and metabolism of G-hesperidin with those of hesperidin in rats. After oral administration of G-hesperidin or hesperidin to rats, hesperetin was detected in sera hydrolyzed with beta-glucuronidase, but it was not detectable in unhydrolyzed sera. Serum hesperetin was found more rapidly in rats administered G-hesperidin than in those administered hesperidin. The area under the concentration-time curve for hesperetin in the sera of rats administered G-hesperidin was approximately 3.7-fold greater than that of rats administered hesperidin. In the urine of both administration groups, hesperetin and its glucuronide were found. Urinary excretion of metabolites was higher in rats administered G-hesperidin than in those administered hesperidin. These results indicate that G-hesperidin presents the same metabolic profile as hesperidin. Moreover, it was concluded that G-hesperidin is absorbed more rapidly and efficiently than hesperidin, because of its high water solubility.


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