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银杏叶提取物(EGb761)在未成熟大鼠子宫增重试验中未表现出雌激素活性。

Ginkgo biloba extract (EGb761) did not express estrogenic activity in an immature rat uterotrophic assay.

作者信息

Moon Byeonghak, Kim Wonchan, Park Cho Hee, Oh Seung Min

机构信息

Department of Nanofusion Technology, Hoseo University, Asan, Republic of Korea.

AB solution, Suwon, Republic of Korea.

出版信息

Environ Health Toxicol. 2018 Sep;33(3):e2018016-0. doi: 10.5620/eht.e2018016. Epub 2018 Sep 28.

Abstract

Ginkgo biloba is a dioecious tree that has been used in traditional Chinese medicine for about 5,000 years. In previous studies on ginkgo biloba extract (EGb761) using in vitro systems, we confirmed that EGb761 has biphasic effects on estrogenicity. In this study, we evaluated the agonistic and antagonistic activities of EGb761 using a uterotrophic assay in immature female rats. To evaluate agonistic and antagonistic effects of EGb761 on uterus, 21-day-old immature Sprague-Dawley (SD) female rats were treated with EGb761 (100, 200, or 400 mg/kg) by oral gavage, 10 μg/kg of estradiol (E2) or 1 mg/kg tamoxifen (TM) by subcutaneous injection, or with EGb761 plus E2 or TM for 3 consecutive days. At the end of the treatment period, animals were sacrificed and their body weights and organ weights (liver, lung, spleen and kidney) were measured. In addition, estrogen-related gene expressions (IGFBP-1 in liver and CaBP-9 in uterus) were determined. During the experiment, no animal showed clinical signs, a change in body weight or died. EGb761 treatment alone had no effect on absolute/relative uterine weight, luminal epithelial cell height (LECH, μm), or luminal circumference (LC, μm). In addition, uterine weights, LECHs, and LC induced by E2 or TM were not significantly changed by EGb761 at any dose. These results collectively suggested EGb761 has no agonistic/antagonistic effects in utero.

摘要

银杏是一种雌雄异株的树木,在传统中医中已使用了约5000年。在之前使用体外系统对银杏叶提取物(EGb761)进行的研究中,我们证实EGb761对雌激素活性具有双相作用。在本研究中,我们使用未成熟雌性大鼠的子宫增重试验评估了EGb761的激动和拮抗活性。为了评估EGb761对子宫的激动和拮抗作用,对21日龄未成熟的Sprague-Dawley(SD)雌性大鼠通过灌胃给予EGb761(100、200或400mg/kg),通过皮下注射给予10μg/kg雌二醇(E2)或1mg/kg他莫昔芬(TM),或给予EGb761加E2或TM,连续3天。在治疗期结束时,处死动物并测量其体重和器官重量(肝脏、肺、脾脏和肾脏)。此外,还测定了雌激素相关基因表达(肝脏中的IGFBP-1和子宫中的CaBP-9)。在实验过程中,没有动物出现临床症状、体重变化或死亡。单独使用EGb761治疗对绝对/相对子宫重量、腔上皮细胞高度(LECH,μm)或腔周长(LC,μm)没有影响。此外,EGb761在任何剂量下都不会显著改变由E2或TM诱导的子宫重量、LECH和LC。这些结果共同表明EGb761在子宫内没有激动/拮抗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b61/6182247/595a86ea8f28/eht-33-3-e2018016f1.jpg

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