Effect of anthocyanin-rich bilberry extract on bone metabolism in ovariectomized rats

• Published in: Biomedical reports Vol. 8; no. 2; pp. 198 - 204
• Main Authors: Shimizu, Saki, Matsushita, Hiroshi, Morii, Yuko, Ohyama, Yuriko, Morita, Noriko, Tachibana, Rika, Watanabe, Kazushi, Wakatsuki, Akihiko
• Format: Journal Article
• Language: English
• Published: England Spandidos Publications 01.02.2018; Spandidos Publications UK Ltd; D.A. Spandidos
• Subjects: Anthocyanins; Berries; Biocompatibility; Biomedical materials; Body weight; Bone density; Bone growth; Bone histomorphometry; Bone loss; Bone mass; Bone mineral density; Bone surgery; Bone turnover; Cancellous bone; Femur; Fruits; Hormone replacement therapy; Menopause; Metabolism; Nutrients; Osteogenesis; Osteoid; Osteoporosis; Ovariectomy; Oxidative stress; Pathogenesis; Physiological aspects; Post-menopause; Postmenopausal women; Rats; Rodents; Supplements; Vegetables; Womens health; Japan; bilberry; bone mineral density; bone histomorphometry; menopause; rat; anthocyanin; osteoporosis; ovariectomy
• ISSN: 2049-9434; 2049-9442
• DOI: 10.3892/br.2017.1029

Menopause is associated with increased oxidative stress, which serves a role, in part, in the pathogenesis of postmenopausal bone loss. Fruits and vegetables are rich in antioxidative nutrients and phytochemicals. Berries are a natural source of anthocyanins, and their intake may improve bone health. The aim of the present study was to determine the effect of an anthocyanin-rich bilberry extract (VME) on bone metabolism in an ovariectomized (Ovx) rat. Female Sprague-Dawley rats (12 weeks old) were randomly divided into the following four groups: Baseline, Sham, Ovx and Ovx+VME (n=8-12 rats per group). Rats in the Baseline group were sacrificed immediately, while those in the other groups were subjected to either sham operation (Sham) or bilateral Ovx (Ovx and Ovx+VME). Rats in the Ovx+VME group were administered VME daily at a dose of 500 mg/kg body weight. At 8 weeks after surgery, bone mass and bone histomorphometry were evaluated. The femur bone mineral density (BMD) in the Ovx group was significantly lower than that in the Sham group (P<0.01). Supplementation of VME in the Ovx rats did not result in an increase in BMD. Histomorphometric analyses revealed that Ovx resulted in decreased measures of bone volume and trabecular number and increased measures of osteoid volume, mineralizing surface and bone formation rates (all P<0.01), whereas VME had no significant effects on these parameters. The present findings indicate that VME did not alter bone metabolism in Ovx rats, suggesting that consumption of VME may not be helpful in preventing postmenopausal bone loss.