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用[具体物质]发酵的[植物名称]根及(.)美林提取物对去卵巢小鼠的抗血脂异常作用 。 需注意,原文中“(.) Merrill”部分表述不太清晰准确,可能存在信息缺失。

Anti-dyslipidemic effects of root and (.) Merrill extracts fermented with in ovariectomized mice.

作者信息

Jang Hyo-Min, Ha Jimyeong, Choi Insuk

机构信息

The 2nd Research Institute CMG Pharmaceutical Co., Ltd. Seongnam Korea.

Center for Consumer Health 1 Research CHA Advanced Research Institute Seongnam Korea.

出版信息

Food Sci Nutr. 2024 Jul 29;12(10):7544-7551. doi: 10.1002/fsn3.4356. eCollection 2024 Oct.

Abstract

root and () Merrill are rich in phytoestrogens. However, these bioactive ingredients have limited bioavailability due to their high molecular weight. In this study, we extracted two natural products and fermented with before mixing the fermented extracts (FPE-FGE). To understand whether FPE-FGE could alleviate menopause with dyslipidemia, we examined their effects on ovariectomy (OVX)-induced dyslipidemia in mice. Oral administration of the FPE-FGE (1:9, 3:7, and 9:1) did not affect safety-related biomarkers, such as uterus index (%), vagina index (%), aspartate aminotransferase, alanine aminotransferase, blood urea nitrogen, and creatinine. Furthermore, FPE-FGE (1:9, 3:7, and 9:1) increased the levels of 17β-estradiol (E2) and expression of uterus estrogen receptor β (ERβ); there was little effect on the expression of uterus estrogen receptor α (ERα), and reduced the levels of gonadotropins, such as luteinizing hormone (LH) and follicle-stimulating hormone (FSH). However, only the FPE-FGE (3:7) reduced the levels of blood lipids, including total cholesterol (TC) and LDL-cholesterol (LDL-C). Accordingly, FPE-FGE (3:7) upregulated endothelial nitric oxide synthase (eNOS), nitric oxide (NO), cyclic guanosine monophosphate (cGMP), and protein kinase G (PKG). In conclusion, FPE-FGE (3:7) attenuated the menopausal dyslipidemia by upregulating eNOS-NO-cGMP signaling pathway.

摘要

[植物名称]的根和()梅里尔富含植物雌激素。然而,由于这些生物活性成分分子量高,其生物利用度有限。在本研究中,我们提取了两种天然产物并用[发酵剂名称]进行发酵,然后将发酵提取物混合(FPE - FGE)。为了解FPE - FGE是否能缓解伴有血脂异常的更年期症状,我们研究了它们对卵巢切除(OVX)诱导的小鼠血脂异常的影响。口服FPE - FGE(1:9、3:7和9:1)对与安全相关的生物标志物没有影响,如子宫指数(%)、阴道指数(%)、天冬氨酸转氨酶、丙氨酸转氨酶、血尿素氮和肌酐。此外,FPE - FGE(1:9、3:7和9:1)提高了17β - 雌二醇(E2)水平和子宫雌激素受体β(ERβ)的表达;对子宫雌激素受体α(ERα)的表达影响很小,并降低了促性腺激素水平,如促黄体生成素(LH)和促卵泡生成激素(FSH)。然而,只有FPE - FGE(3:7)降低了血脂水平,包括总胆固醇(TC)和低密度脂蛋白胆固醇(LDL - C)。因此,FPE - FGE(3:7)上调了内皮型一氧化氮合酶(eNOS)、一氧化氮(NO)、环磷酸鸟苷(cGMP)和蛋白激酶G(PKG)。总之,FPE - FGE(3:7)通过上调eNOS - NO - cGMP信号通路减轻了更年期血脂异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285b/11521700/87390b52c24f/FSN3-12-7544-g001.jpg

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