TY - JOUR
T1 - Ginkgo biloba extract EGb 761 attenuates hippocampal neuronal loss and cognitive dysfunction resulting from chronic restraint stress in ovariectomized rats
AU - Takuma, K.
AU - Hoshina, Y.
AU - Arai, S.
AU - Himeno, Y.
AU - Matsuo, A.
AU - Funatsu, Y.
AU - Kitahara, Y.
AU - Ibi, D.
AU - Hayase, M.
AU - Kamei, H.
AU - Mizoguchi, H.
AU - Nagai, T.
AU - Koike, K.
AU - Inoue, M.
AU - Yamada, K.
N1 - Funding Information:
We are grateful to Dr. Wolfgang Weber (Dr. Willmar Schwabe GmbH & Co. KG, Karlsruhe, Germany) and Dr. Yoichiro Ueno (Schwabe Greenwave Ltd., Tokyo, Japan) for providing Ginkgo biloba leaf extract EGb 761 and giving valuable advice. This study was supported in part by Grants for Scientific Research (19390062) and for the 21st Century COE Program from the Ministry of Education, Culture, Sports, Science and Technology of Japan, a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science, a grant from Kanzawa Medical Research Foundation, and a grant from the Smoking Research Foundation.
PY - 2007/10/26
Y1 - 2007/10/26
N2 - We have recently found that a combination of ovariectomy (OVX) and chronic restraint stress causes cognitive dysfunction and reduces hippocampal CA3 neurons in female rats and that estrogen replacement suppresses the OVX/stress-induced behavioral and morphological changes. In this study, we examined the effect of Ginkgo biloba extract (EGb 761), a popular herbal supplement, on the cognitive dysfunction and neuromorphological change in OVX/stress-subjected rats. Female Fisher 344 rats were randomly divided into three groups: vehicle-treated OVX, EGb 761 (50 mg/kg) -treated OVX and vehicle-treated sham-operated control groups. Two months after ovariectomy, all animals received restraint stress for 21 days (6 h/day), and were then subjected to a novel object recognition test followed by morphological examination by Nissl staining. EGb 761 was orally administered once daily until the behavioral analysis was done. Treatment with EGb 761 improved memory impairment and neuronal loss of hippocampus in the OVX/stress-subjected group in the same ways as 17β-estradiol. On the other hand, EGb 761 did not affect the loss of bone mineral density and increase in body weight after OVX, although 17β-estradiol attenuated them. These results have important implications for neuroprotective and cognition enhancing effects of EGb 761 in postmenopausal women and suggest that the effects are mediated by a different mechanism from estrogen.
AB - We have recently found that a combination of ovariectomy (OVX) and chronic restraint stress causes cognitive dysfunction and reduces hippocampal CA3 neurons in female rats and that estrogen replacement suppresses the OVX/stress-induced behavioral and morphological changes. In this study, we examined the effect of Ginkgo biloba extract (EGb 761), a popular herbal supplement, on the cognitive dysfunction and neuromorphological change in OVX/stress-subjected rats. Female Fisher 344 rats were randomly divided into three groups: vehicle-treated OVX, EGb 761 (50 mg/kg) -treated OVX and vehicle-treated sham-operated control groups. Two months after ovariectomy, all animals received restraint stress for 21 days (6 h/day), and were then subjected to a novel object recognition test followed by morphological examination by Nissl staining. EGb 761 was orally administered once daily until the behavioral analysis was done. Treatment with EGb 761 improved memory impairment and neuronal loss of hippocampus in the OVX/stress-subjected group in the same ways as 17β-estradiol. On the other hand, EGb 761 did not affect the loss of bone mineral density and increase in body weight after OVX, although 17β-estradiol attenuated them. These results have important implications for neuroprotective and cognition enhancing effects of EGb 761 in postmenopausal women and suggest that the effects are mediated by a different mechanism from estrogen.
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U2 - 10.1016/j.neuroscience.2007.07.042
DO - 10.1016/j.neuroscience.2007.07.042
M3 - Article
C2 - 17869007
AN - SCOPUS:35348922970
SN - 0306-4522
VL - 149
SP - 256
EP - 262
JO - Neuroscience
JF - Neuroscience
IS - 2
ER -