Summary
Recent studies have suggested that green tea polyphenols (GTP) are promising agents for preventing bone loss in women. Findings
that GTP supplementation resulted in increased urinary GTP concentrations and bone mass via an increase of antioxidant capacity
and/or a decrease of oxidative stress damage suggest a significant role of GTP in bone health of women.
Introduction
Recent studies suggested that green tea polyphenols (GTP) are promising agents for preventing bone loss in women. However,
the mechanism related to the possible protective role of GTP in bone loss is not well understood.
Methods
This study evaluated bioavailability, mechanisms, bone mass, and safety of GTP in preventing bone loss in middle-aged rats
without (sham, SH) and with ovariectomy (OVX). A 16-week study of 2 (SH vs. OVX) × 3 (no GTP, 0.1% GTP, and 0.5% GTP in drinking
water) factorial design using 14-month-old female rats (n = 10/group) was performed. An additional 10 rats in baseline group were euthanized at the beginning of study to provide baseline
parameters.
Results
There was no difference in femur bone mineral density between baseline and the SH+0.5% GTP group. Ovariectomy resulted in
lower values for liver glutathione peroxidase activity, serum estradiol, and bone mineral density. GTP supplementation resulted
in increased urinary epigallocatechin and epicatechin concentrations, liver glutathione peroxidase activity and femur bone
mineral density, decreased urinary 8-hydroxy-2′-deoxyguanosine and urinary calcium levels, but no effect on serum estradiol
and blood chemistry levels.
Conclusion
We conclude that a bone-protective role of GTP may contribute to an increase of antioxidant capacity and/or a decrease of
oxidative stress damage.
Keywords Blood chemistry - Bone mineral density - Green tea - Oxidative stress - Postmenopausal women
Originally presented as “Green Tea Polyphenols Prevent Aging- and Estrogen-Deficiency-Induced Bone Loss in Aged and Ovariectomized
Female Rats” by Chwan-Li Shen at the Annual Meeting of Experimental Biology held in Washington D.C., USA, April 27-May 1,
2007.
Supported by Lubbock Endowed Professorship to CLS and NIH grant CA90997 to JSW.