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中國精品科技期刊2020
尹忞強,羅來慶,湯海蓮,等. 銀杏內酯B對肥胖小鼠的改善作用研究[J]. 食品工業科技,2024,45(6):337?342. doi: 10.13386/j.issn1002-0306.2023050132.
引用本文: 尹忞強,羅來慶,湯海蓮,等. 銀杏內酯B對肥胖小鼠的改善作用研究[J]. 食品工業科技,2024,45(6):337?342. doi: 10.13386/j.issn1002-0306.2023050132.
YIN Minqiang, LUO Laiqing, TANG Hailian, et al. Ameliorating Effect of Ginkgolide B on Obese Mice[J]. Science and Technology of Food Industry, 2024, 45(6): 337?342. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023050132.
Citation: YIN Minqiang, LUO Laiqing, TANG Hailian, et al. Ameliorating Effect of Ginkgolide B on Obese Mice[J]. Science and Technology of Food Industry, 2024, 45(6): 337?342. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023050132.

銀杏內酯B對肥胖小鼠的改善作用研究

Ameliorating Effect of Ginkgolide B on Obese Mice

  • 摘要: 為探究銀杏內酯B(ginkgolide B,GB)對肥胖小鼠的干預作用,首先采用高脂膳食誘導構建C57BL/6J小鼠肥胖模型,隨后將肥胖小鼠按體重隨機分為4組,模型組(PG)、GB低劑量組(GBL)、GB中劑量組(GBM)和GB高劑量組(GBH),進行為期8周的干預實驗,測定各組小鼠肥胖相關指標,如體重變化、臟器脂肪系數、血脂指標等。GB干預后,GBM和GBH組小鼠的體重增長明顯小于PG組(P<0.05),同時,GBH組的小鼠臟器脂肪系數均顯著降低(P<0.05)。另外,GBM和GBH組小鼠的血脂指標總膽固醇(total cholesterol,TC)、甘油三酯(triglyceride,TG)、低密度脂蛋白膽固醇(low density lipoprotein cholesterol,LDL-C)、高密度脂蛋白膽固醇(high density lipoprotein cholesterol,HLD-C)均得到顯著(P<0.05)改善,尤其是GBH組小鼠;最后,組織病理學結果顯示,GBM和GBH組小鼠肝臟脂肪沉積明顯減輕。進一步實時熒光定量聚合酶鏈式反應(Quantitative Real-time Polymerase Chain Reaction,qRT-PCR)結果顯示,和PG組相比,GBM和GBH組小鼠肝臟中過氧化物酶體增殖物激活受體γ(peroxisome proliferator-activated receptorγ,PPARγ)的mRNA表達水平顯著降低(P<0.05),而解偶聯蛋白2(Uncoupling protein 2,UCP-2)的mRNA水平顯著增加(P<0.05)。本研究發現中高劑量的GB可以有效改善小鼠的肥胖,并且這種改善作用可能和PPARγ-UCP-2信號途徑相關。

     

    Abstract: This study aims to explore the effect of ginkgolide B (GB) on obese mice. An obese C57BL/6J mice model was induced by high-fat diet firstly, and then the obese mice were divided into 4 groups according to body weight randomly: Positive model group (PG), GB low dose group (GBL), GB medium dose group (GBM) and GB high dose group (GBH). After 8-week intervention, the obesity-related indexes (weight change, visceral fat coefficient and serum indexes) of mice in each group were measured. Results showed that the weight gain of mice in GBM and GBH were significantly decreased than in PG (P<0.05), and the visceral fat coefficient of mice in GBH group was also reduced significantly (P<0.05) after GB treatment. Meanwhile, the serum indexes (TG, TC, LDL-C and HDL-C) of mice in GBM and GBH were obviously improved, especially in GBH. Besides, histopathologic findings showed that liver fat deposition was apparently reduced in GBM and GBH. Furthermore, qRT-PCR results showed that the mRNA expression level of PPARγ in liver of mice in GBM and GBH was significantly decreased (P<0.05) in comparison with PG, while the mRNA expression level of UCP-2 was significantly increased (P<0.05). In summary, this study demonstrated that GB of medium and high doses improved obesity in mice, and this ameliorating effect might be related to PPARγ-UCP-2 signaling pathway.

     

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