Menu  → Metabolism information on chemical compounds  → 
Hesperetin 7-glucoside
Hesperetin 7-glucoside

Compound Hesperetin 7-glucoside 
Animal species rat 
Metabolism parameters  
Metabolites Hesperetin 7-glucoside
Crude drug Citrus Unshiu Peel 
References 1) Véronique Habauzit, Inge-Lise Nielsen, Angel Gil-Izquierdo, Anna Trzeciakiewicz, Christine Morand, Winnie Chee, Denis Barron, Patrice Lebecque, Marie-Jeanne Davicco, Gary Williamson, Elizabeth Offord, Véronique Coxam and Marie-Noëlle Horcajada: Increased bioavailability of hesperetin-7-glucoside compared with hesperidin results in more efficient prevention of bone loss in adult ovariectomised rats. British Journal of Nutrition, 102, 976–984 (2009). 
Remarks Wistar rats were sham operated or ovariectomised (OVX), then pair fed for 90 d a casein-based diet supplemented or not with freeze-dried orange juice enriched with hesperidin (Hp) or hesperetin 7-glucoside (H-7-glc) at two doses of 0.25 and 0.5 % (hesperetin basis). In the rats fed 0.5%, a reduction in OVX-induced bone loss was observed regarding total bone mineral density (BMD): + 7.0% in OVX rats treated with Hp (HpOVX) and +6.6% in OVX rats treated with H-7-glc (H-7-glcOVX) v. OVX controls (p<0.05). In the rats fed 0.25% diet, the H-7-glc OVX group showed a 6.6% improvement in BMD v. the OVX controls (p<0.05), whereas the Hp diet had no effect at this dose. The BMD of rats fed 0.25% H-7-glc was equal to that of those given 0.5% Hp, but was not further increased at 0.5% H-7-glc. Plasma hesperetin levels and relative urinary excretion were significantly enhanced in the H-7-glc v. Hp groups, and the metabolite profile showed the absence of eriodictyol metabolites and increased levels of hesperetin sulphates. Taken together, improved bioavailability of H-7-glc may explain the more efficient bone protection of this compound. 
 

TOPICS

Information on genetic analysis

Information of bioassay

Metabolism information on chemical compounds included in crude drugs

Traditional Medical & Pharmaceutical Database


Section of Pharmacognosy,
Division of Medicinal Resources,
Department of Research and Development,
Institute of Natural Medicine,
University of Toyama
2630 Sugitani, Toyama 930-0194 Japan
TEL: +81-76-434-7601
FAX: +81-76-434-5064