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D-Pinitol attenuates postmenopausal symptoms in ovariectomized mice

去卵巢大鼠 内分泌学 内科学 高架加迷宫 突触素 雌激素 医学 更年期 齿状回 尾部悬挂试验 行为绝望测验 海马体 焦虑 精神科 免疫组织化学 抗抑郁药
作者
Woo Chang Kang,Keontae Park,Chang Hyeon Kong,Do Yeon Kim,Yong Seung Lee,Mijin Jeon,Min Seo Kim,Seo Yun Jung,Jongki Hong,Jung Hye Choi,Jong Hoon Ryu
出处
期刊:Life Sciences [Elsevier BV]
卷期号:333: 122147-122147 被引量:9
标识
DOI:10.1016/j.lfs.2023.122147
摘要

Menopause is a natural process in women that can lead to post-menopausal syndrome with symptoms such as hot flushes, weight gain, anxiety, cognitive decline, and depression. Hormonal replacement therapy is commonly prescribed. However, it has serious adverse effects. Herbal medicinal products and isoflavones are used as alternatives. D-Pinitol found in Pinaceae and Fabaceae families has anti-inflammatory and antioxidant effects. However, it has not received as much attention as isoflavones. In this study, we investigated whether D-pinitol could alleviate post-menopausal symptoms using an ovariectomized (OVX) mouse model. Female ICR mice were divided into six groups: sham (vehicle), OVX (vehicle), OVX + D-pinitol (10, 30, 100 mg/kg, p.o.), and OVX + estradiol (0.5 mg/kg, s.c.). Treatment with vehicle, D-pinitol, and estradiol began at seven weeks post ovariectomy. We employed several behavioral tests, hot-flush test, and Western blot analysis. We found that D-pinitol treatment (30, 100 mg/kg, p.o.) reversed cognitive dysfunction in OVX mice (novel object recognition and Y-maze test). Additionally, D-pinitol alleviated anxiety-like behaviors (elevated plus-maze) and reversed depressive-like behaviors (splash test, tail suspension test). It also normalized increased basal tail skin temperature in OVX mice. Moreover, D-pinitol administration reversed decreased expression of ERβ and synaptophysin and phosphorylation of ERK and PI3K-Akt-GSK-3β induced by OVX in the hippocampus and prefrontal cortex. These findings indicate that D-pinitol might be a promising candidate for treating post-menopausal symptoms by increasing ERβ and synaptophysin expression levels and activation of ERK or PI3K-Akt-GSK-3β signaling pathway, at least in part.
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